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Gene: BDNF (brain derived neurotrophic factor) Homo sapiens

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Symbol:

BDNF

Name:

brain derived neurotrophic factor

RGD ID:

731027

HGNC Page

HGNC:1033

Description:

Predicted to enable growth factor activity and nerve growth factor receptor binding activity. Involved in nervous system development and positive regulation of nervous system development. Predicted to be located in perinuclear region of cytoplasm and secretory granule. Predicted to be active in several cellular components, including glutamatergic synapse; hippocampal mossy fiber to CA3 synapse; and secretory vesicle. Implicated in several diseases, including alcohol dependence; cocaine dependence; cognitive disorder (multiple); congenital central hypoventilation syndrome; and neurodegenerative disease (multiple). Biomarker of several diseases, including lung disease (multiple); mood disorder (multiple); neurodegenerative disease (multiple); open-angle glaucoma (multiple); and opiate dependence (multiple).

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

abrineurin; ANON2; brain-derived neurotrophic factor; BULN2; MGC34632; neurotrophic factor BDNF precursor form; neurotrophin; proBDNF

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Bdnf (brain derived neurotrophic factor)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Bdnf (brain-derived neurotrophic factor)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB
Chinchilla lanigera (long-tailed chinchilla):	Bdnf (brain derived neurotrophic factor)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	BDNF (brain derived neurotrophic factor)	NCBI	Ortholog
Canis lupus familiaris (dog):	BDNF (brain derived neurotrophic factor)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Bdnf (brain derived neurotrophic factor)	NCBI	Ortholog
Sus scrofa (pig):	BDNF (brain derived neurotrophic factor)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	BDNF (brain derived neurotrophic factor)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Bdnf (brain derived neurotrophic factor)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Bdnf (brain-derived neurotrophic factor)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Bdnf (brain derived neurotrophic factor)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	bdnf (brain-derived neurotrophic factor)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Xenopus tropicalis (tropical clawed frog):	bdnf	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	bdnf	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	bdnf.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	bdnf.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	27,654,893 - 27,722,030 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	27,654,893 - 27,722,058 (-)	Ensembl			hg38	GRCh38
GRCh37	11	27,676,440 - 27,743,577 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	27,633,016 - 27,699,872 (-)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	11	27,633,019 - 27,637,249	NCBI
Celera	11	27,822,548 - 27,889,725 (-)	NCBI		Celera
Cytogenetic Map	11	p14.1	NCBI
HuRef	11	27,374,586 - 27,441,772 (-)	NCBI		HuRef
CHM1_1	11	27,675,184 - 27,742,527 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	27,795,301 - 27,862,460 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

acoustic neuroma (IEP)

acute stress disorder (ISO)

alcohol dependence (IAGP,ISO)

alcohol use disorder (IEP,ISO)

alcohol withdrawal syndrome (IEP,ISO)

Alcohol-Related Disorders (ISO)

Alcoholic Intoxication (ISO)

alopecia (IEP)

Alzheimer's disease (EXP,IAGP,IEA,IEP,ISO)

amnestic disorder (ISO)

amphetamine abuse (EXP,ISO)

Amyloid Plaques (ISO)

Anhedonia (ISO)

anxiety disorder (ISO)

Arthralgia (ISO)

asthma (IAGP,IDA,IEP)

Ataxia (ISO)

atopic dermatitis (IAGP,IEP)

attention deficit hyperactivity disorder (ISO)

autism spectrum disorder (EXP,IEP)

autistic disorder (EXP)

bacterial meningitis (ISO)

Binge Drinking (ISO)

bipolar disorder (EXP,IEA)

Body Weight (EXP)

borna disease (ISO)

Brain Injuries (EXP,IEP)

brain ischemia (EXP)

cannabis abuse (ISO)

Cerebral Hemorrhage (IMP)

Chronic Pain (ISO)

cocaine abuse (ISO)

cocaine dependence (IDA,ISO)

Cocaine-Related Disorders (EXP,ISO)

cognitive disorder (IAGP,ISO)

colitis (ISO)

color blindness (IAGP)

congenital central hypoventilation syndrome (IAGP)

cystitis (ISO)

Deafness (EXP,IDA,ISO)

depressive disorder (EXP,IEP,ISO)

Diabetic Nephropathies (ISO)

diabetic neuropathy (ISO)

diabetic retinopathy (ISO)

Drug Eruptions (ISO)

Dysbiosis (ISO)

epilepsy (EXP)

epilepsy with generalized tonic-clonic seizures (EXP)

Experimental Autoimmune Encephalomyelitis (ISO)

Experimental Diabetes Mellitus (ISO)

Experimental Seizures (ISO)

focal epilepsy (IEA)

Frontotemporal Lobar Degeneration (IAGP)

genetic disease (IAGP)

glaucoma (IDA,IMP,ISO)

Gliosis (EXP)

Hearing Loss (ISO)

Hearing Loss, Noise-Induced (ISO)

heroin dependence (EXP,IEP)

Huntington's disease (IEP,IMP,ISO)

Hyperalgesia (IDA,ISO)

Hyperoxia (ISO)

hypertensive encephalopathy (ISO)

hypothyroidism (ISO)

Hypoxia (EXP)

Inflammation (EXP,ISO)

inner ear disease (ISO)

intellectual disability (EXP,IAGP)

intermediate coronary syndrome (IEP)

interstitial lung disease (IEP)

Intervertebral Disc Disease (IEP)

Intervertebral Disc Displacement (ISO)

intestinal disease (ISO)

irritable bowel syndrome (IEP)

keratoconus (IEP)

Leukoencephalopathies (ISO)

low tension glaucoma (IEP)

major depressive disorder (IEP)

Memory Disorders (IAGP,IEP,ISO)

Metabolic Syndrome (IEP)

middle cerebral artery infarction (ISO)

mood disorder (IEP)

morbid obesity (EXP)

morphine dependence (ISO)

morphine withdrawal syndrome (ISO)

multiple sclerosis (IEP)

Nasal Polyps (IEP)

neovascular inflammatory vitreoretinopathy (IEP)

Nerve Degeneration (EXP,ISO)

Nerve Injuries (ISO)

nervous system disease (EXP)

nicotine dependence (EXP,ISO)

obesity (IAGP,IEP)

obsessive-compulsive disorder (IAGP,ISO)

obstructive sleep apnea (IDA)

opiate dependence (IEP)

Optic Nerve Injuries (IDA,ISO)

Pain (ISO)

Parkinson's disease (EXP,IAGP,IEA,IEP)

Parkinsonism (IDA)

Peripheral Nerve Injuries (ISO)

post-traumatic stress disorder (IAGP,ISO)

Postoperative Cognitive Dysfunction (IEP,ISO)

premature ejaculation (ISO)

Prenatal Exposure Delayed Effects (ISO)

Presbycusis (ISO)

primary open angle glaucoma (IEP)

psychotic disorder (EXP)

pulmonary fibrosis (IEP)

pulmonary sarcoidosis (IEP)

Radiation Injuries (ISO)

Referred Pain (ISO)

Reperfusion Injury (ISO)

Respiration Disorders (ISO)

Respiratory Tract Infections (IEP)

Retina Reperfusion Injury (IDA)

retinal degeneration (ISO)

rhinitis (IAGP,ISO)

schizophrenia (EXP,IEA)

sciatic neuropathy (ISO)

Seasonal Allergic Rhinitis (IEP)

sensorineural hearing loss (ISO)

Sjogren's syndrome (IEP)

Sleep Deprivation (ISO)

Spinal Cord Injuries (IMP,ISO)

Spinal Cord Reperfusion Injury (ISO)

Starvation (ISO)

status epilepticus (EXP,IMP,ISO)

Stomach Neoplasms (EXP)

Stroke (ISO)

systemic scleroderma (IEP)

Tinnitus (IEP,ISO)

transient cerebral ischemia (ISO)

traumatic brain injury (ISO)

trigeminal neuralgia (ISO)

type 2 diabetes mellitus (IEP)

urticaria (IEP)

vascular dementia (ISO)

Visceral Pain (ISO)

withdrawal disorder (EXP,ISO)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (ISO)

(+)-epicatechin-3-O-gallate (EXP)

(+)-pilocarpine (ISO)

(+)-syringaresinol beta-D-glucoside (ISO)

(-)-epigallocatechin 3-gallate (EXP,ISO)

(20S)-ginsenoside Rg3 (EXP,ISO)

(R)-salsolinol (ISO)

(R,R,R)-alpha-tocopherol (ISO)

(S)-3,5-dihydroxyphenylglycine (ISO)

(S)-AMPA (ISO)

(S)-amphetamine (EXP,ISO)

(S)-colchicine (ISO)

(S)-naringenin (ISO)

(S)-nicotine (EXP,ISO)

1,1-dichloroethene (ISO)

1,2-dimethylhydrazine (ISO)

1-bromopropane (EXP,ISO)

1-chloro-2,4-dinitrobenzene (ISO)

1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (ISO)

1-naphthol (EXP)

13,14-dihydro-Delta(12)-prostaglandin J2 (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP,ISO)

17beta-estradiol 3-benzoate (ISO)

2,2',4,4'-Tetrabromodiphenyl ether (ISO)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

2,3,7,8-Tetrachlorodibenzofuran (ISO)

2,3-Dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline (ISO)

2,4-dibromophenyl 2,4,5-tribromophenyl ether (ISO)

2,5-hexanedione (ISO)

2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine (ISO)

2-amino-2-deoxy-D-glucopyranose (ISO)

2-Hydroxy-6-(8,11,14-pentadecatrienyl)benzoic acid (ISO)

2-methyl-6-(phenylethynyl)pyridine (ISO)

2-palmitoylglycerol (EXP)

3',5'-cyclic AMP (EXP)

3,3',5,5'-tetrabromobisphenol A (EXP,ISO)

3,4-dihydroxybenzoic acid (ISO)

3,4-methylenedioxymethamphetamine (ISO)

3-isobutyl-1-methyl-7H-xanthine (EXP)

3-Methoxynobiletin (ISO)

3-nitropropanoic acid (ISO)

3H-1,2-dithiole-3-thione (ISO)

4,4'-sulfonyldiphenol (EXP,ISO)

4,5,6,7-TETRABROMOBENZOTRIAZOLE (ISO)

4-[1-hydroxy-2-[4-(phenylmethyl)-1-piperidinyl]propyl]phenol (ISO)

4-hydroxynon-2-enal (ISO)

5-aza-2'-deoxycytidine (EXP,ISO)

5-azacytidine (ISO)

5-fluorouracil (ISO)

5-methoxypsoralen (ISO)

6-anilino-5,8-quinolinedione (EXP)

6-Cyano-7-nitroquinoxaline-2,3-dione (ISO)

6-propyl-2-thiouracil (ISO)

7,12-dimethyltetraphene (ISO)

[6]-Shogaol (ISO)

AB-Fubinaca (ISO)

acetylsalicylic acid (ISO)

acrolein (ISO)

acrylamide (ISO)

actinomycin D (ISO)

aflatoxin B1 (EXP,ISO)

agathisflavone (ISO)

agmatine (ISO)

agomelatine (ISO)

alcohol (ISO)

aldehydo-D-glucosamine (ISO)

all-trans-retinoic acid (EXP,ISO)

alpha-D-galactose (ISO)

alpha-pinene (ISO)

alpha-Solamarine (ISO)

aluminium hydroxide (EXP)

AM-251 (ISO)

amantadine (ISO)

amiodarone (ISO)

ammonium chloride (ISO)

amphetamine (ISO)

aniracetam (ISO)

anthra[1,9-cd]pyrazol-6(2H)-one (EXP)

apigenin (ISO)

arachidonic acid (EXP)

aristolochic acid A (EXP)

Aroclor 1254 (EXP,ISO)

arsane (EXP,ISO)

arsanilic acid (ISO)

arsenic atom (EXP,ISO)

arsenite(3-) (EXP)

arsenous acid (EXP,ISO)

asiaticoside (ISO)

Atractylone (EXP)

atrazine (EXP,ISO)

Bardoxolone methyl (ISO)

Bay-K-8644 (ISO)

benzo[a]pyrene (EXP,ISO)

benzo[a]pyrene diol epoxide I (EXP)

beta-D-glucosamine (ISO)

bis(2-chloroethyl) sulfide (ISO)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP,ISO)

bisphenol F (EXP,ISO)

bromocriptine (ISO)

bucladesine (EXP)

bupivacaine (EXP)

buprenorphine (ISO)

Butylbenzyl phthalate (ISO)

Butylparaben (ISO)

C60 fullerene (ISO)

cabergoline (EXP)

cadmium atom (EXP,ISO)

cadmium dichloride (EXP,ISO)

caffeine (ISO)

calcitriol (EXP)

calcium atom (EXP,ISO)

calcium(0) (EXP,ISO)

cannabidiol (EXP,ISO)

capsaicin (ISO)

carbamazepine (ISO)

carbon dioxide (ISO)

carbon monoxide (ISO)

carbon nanotube (ISO)

celastrol (ISO)

CGP 52608 (EXP)

CGS-21680 (ISO)

chaetocin (ISO)

chlorohydrocarbon (EXP)

chloroprene (ISO)

chlorpromazine (EXP,ISO)

chlorpyrifos (EXP,ISO)

cholesterol (ISO)

choline (ISO)

chondroitin sulfate (EXP)

chrysin (ISO)

cisplatin (EXP,ISO)

Citreoviridin (ISO)

clofibrate (ISO)

clopidogrel (EXP)

clozapine (ISO)

cocaine (EXP,ISO)

coenzyme Q10 (ISO)

colforsin daropate hydrochloride (EXP,ISO)

copper atom (EXP,ISO)

copper(0) (EXP,ISO)

copper(II) sulfate (ISO)

corticosterone (ISO)

creatine (ISO)

crocidolite asbestos (EXP)

crocin-1 (ISO)

Cuprizon (ISO)

curcumin (ISO)

cyanocob(III)alamin (ISO)

cyclophosphamide (ISO)

cyclosporin A (EXP,ISO)

cyfluthrin (ISO)

cypermethrin (ISO)

daidzein 7-O-beta-D-glucoside (ISO)

dantrolene (ISO)

DDE (EXP,ISO)

DDT (ISO)

decabromodiphenyl ether (ISO)

deguelin (EXP,ISO)

dermatan sulfate (EXP)

desferrioxamine B (ISO)

desipramine (ISO)

dexamethasone (EXP,ISO)

diallyl disulfide (ISO)

diarsenic trioxide (EXP,ISO)

diazepam (ISO)

diazinon (ISO)

dibutyl phthalate (ISO)

dichloroacetic acid (ISO)

diethyl phthalate (ISO)

diethylstilbestrol (EXP,ISO)

dihydroactinidiolide (ISO)

dihydrolipoic acid (EXP)

diisobutyl phthalate (ISO)

diisononyl phthalate (ISO)

diisopropyl fluorophosphate (ISO)

dimethyl fumarate (ISO)

dioxygen (EXP,ISO)

diphenyl diselenide (ISO)

disulfiram (EXP)

dizocilpine maleate (ISO)

donepezil hydrochloride (ISO)

dopamine (ISO)

dorsomorphin (EXP)

doxorubicin (EXP,ISO)

echinacoside (ISO)

elemental selenium (ISO)

endosulfan (ISO)

enzacamene (ISO)

epoxiconazole (ISO)

ethanol (ISO)

ethyl methanesulfonate (EXP)

Ethylenethiourea (EXP)

etoposide (EXP)

eugenol (ISO)

Evodiamine (EXP)

excitatory amino acid agonist (ISO)

Fast green FCF (ISO)

fentanyl (ISO)

fenvalerate (ISO)

ferrostatin-1 (ISO)

fingolimod hydrochloride (ISO)

fisetin (ISO)

fluoranthene (ISO)

fluoxetine (EXP,ISO)

folic acid (ISO)

formaldehyde (EXP,ISO)

fulvestrant (EXP)

Fusaric acid (ISO)

galactose (ISO)

galangin (ISO)

gallic acid (EXP)

gallocatechin (EXP)

gamma-aminobutyric acid (ISO)

gamma-hexachlorocyclohexane (ISO)

Gastrodin (ISO)

gemcitabine (EXP)

genistein (ISO)

gentamycin (ISO)

geraniol (ISO)

gingerol (ISO)

glycidol (ISO)

glycyrrhizinic acid (ISO)

glyphosate (ISO)

haloperidol (EXP,ISO)

herbicide (ISO)

heroin (EXP,ISO)

hydrogen peroxide (EXP,ISO)

ifosfamide (ISO)

imipramine (ISO)

inulin (ISO)

kainic acid (ISO)

ketamine (ISO)

ketanserin (ISO)

KT 5823 (ISO)

L-ascorbic acid (EXP,ISO)

L-methionine (ISO)

lamotrigine (ISO)

lead diacetate (ISO)

lead(0) (ISO)

linuron (ISO)

lipopolysaccharide (ISO)

lithium atom (EXP,ISO)

lithium chloride (EXP)

lithium hydride (EXP,ISO)

lovastatin (ISO)

LY294002 (EXP,ISO)

lycopene (ISO)

malathion (EXP)

maneb (ISO)

manganese atom (EXP,ISO)

manganese(0) (EXP,ISO)

manganese(II) chloride (EXP,ISO)

melatonin (ISO)

melittin (ISO)

mercury atom (EXP)

mercury dibromide (EXP)

mercury dichloride (ISO)

mercury(0) (EXP)

metformin (ISO)

methamphetamine (EXP,ISO)

methyl beta-cyclodextrin (ISO)

methyl methanesulfonate (EXP)

methylglyoxal (EXP)

methyllycaconitine (EXP)

methylmercury chloride (EXP,ISO)

methylphenidate (EXP,ISO)

mevastatin (ISO)

mifepristone (EXP,ISO)

mono(2-ethylhexyl) phthalate (ISO)

monocrotaline (ISO)

morin (ISO)

morphine (ISO)

muscimol (ISO)

N-acetyl-L-cysteine (EXP,ISO)

N-ethyl-N-nitrosourea (ISO)

N-methyl-4-phenylpyridinium (EXP,ISO)

N-methyl-N'-nitro-N-nitrosoguanidine (ISO)

N-methyl-N-nitrosourea (ISO)

naproxen (ISO)

nicardipine (ISO)

nickel atom (EXP)

nicotine (EXP,ISO)

nicotinic acid (ISO)

nifedipine (ISO)

nimodipine (ISO)

nitric oxide (EXP)

Nonylphenol (ISO)

ochratoxin A (ISO)

olanzapine (EXP,ISO)

oleuropein (ISO)

ouabain (ISO)

Oxadiazon (EXP)

oxaliplatin (ISO)

oxidopamine (ISO)

ozone (ISO)

paclitaxel (ISO)

paliperidone palmitate (ISO)

panaxydol (ISO)

papaverine (ISO)

paracetamol (ISO)

paraldehyde (ISO)

paraquat (EXP,ISO)

parathion-methyl (ISO)

paroxetine (ISO)

pentetrazol (ISO)

pentobarbital (ISO)

perchlorate (ISO)

perfluorohexanesulfonic acid (EXP)

perfluorononanoic acid (ISO)

perfluorooctane-1-sulfonic acid (ISO)

permethrin (EXP,ISO)

peroxynitrous acid (ISO)

PF-3758309 (EXP)

phenobarbital (ISO)

phenylephrine (ISO)

phosphorothioic O,O,S-acid (EXP)

picrotoxin (ISO)

pioglitazone (ISO)

poly(I:C) (ISO)

potassium atom (ISO)

potassium chloride (ISO)

potassium chromate (EXP)

prasugrel hydrochloride (ISO)

prochloraz (ISO)

procymidone (ISO)

prodigiosin (ISO)

progesterone (EXP,ISO)

propanal (EXP)

pyrethrins (ISO)

Pyridostigmine bromide (ISO)

pyrrolidine dithiocarbamate (EXP)

quartz (ISO)

quercetin (ISO)

quetiapine fumarate (ISO)

quinolinic acid (ISO)

reserpine (ISO)

resveratrol (ISO)

rimonabant (ISO)

risperidone (EXP,ISO)

ritanserin (ISO)

rivastigmine (ISO)

roflumilast (ISO)

rolipram (ISO)

romidepsin (ISO)

rotenone (EXP,ISO)

royal jelly (ISO)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

salvianolic acid B (ISO)

saroglitazar (ISO)

saxagliptin (ISO)

SB 431542 (EXP)

scopolamine (ISO)

selenium atom (ISO)

serotonin (ISO)

sertraline (ISO)

sevoflurane (ISO)

silver atom (EXP)

silver(0) (EXP)

simvastatin (ISO)

sirolimus (ISO)

SKF-96365 hydrochloride (ISO)

SL-327 (ISO)

sodium arsenate (ISO)

sodium arsenite (EXP,ISO)

sodium fluoride (EXP,ISO)

Soman (ISO)

sterigmatocystin (ISO)

streptozocin (ISO)

sulforaphane (EXP)

sumatriptan (ISO)

tacrine (ISO)

tacrolimus hydrate (ISO)

tadalafil (ISO)

tamibarotene (EXP,ISO)

tamoxifen (EXP,ISO)

taurine (EXP,ISO)

telmisartan (ISO)

tert-butyl hydroperoxide (EXP)

Testosterone propionate (ISO)

tetrodotoxin (EXP,ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

toluene (ISO)

topiramate (ISO)

torcetrapib (EXP)

tranylcypromine (ISO)

triacsin C (EXP)

triazolam (ISO)

triazophos (ISO)

trichloroethene (ISO)

trichostatin A (EXP,ISO)

undecane (ISO)

valproic acid (EXP,ISO)

venlafaxine hydrochloride (ISO)

veratridine (ISO)

vinclozolin (ISO)

vorinostat (ISO)

vortioxetine (ISO)

VX nerve agent (EXP,ISO)

wortmannin (ISO)

xenon atom (ISO)

xenon(0) (ISO)

zearalenone (EXP)

zinc atom (ISO)

zinc dichloride (ISO)

zinc sulfate (EXP,ISO)

zinc(0) (ISO)

zolpidem (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

axon extension (ISO)

axon guidance (ISO,TAS)

axon target recognition (ISO)

behavioral fear response (ISO)

behavioral response to cocaine (ISO)

brain-derived neurotrophic factor receptor signaling pathway (TAS)

cell surface receptor protein tyrosine kinase signaling pathway (IBA)

cellular response to nerve growth factor stimulus (ISO)

cellular response to norepinephrine stimulus (ISO)

cellular response to potassium ion (ISO)

cellular response to tumor necrosis factor (ISO)

chronic inflammatory response (ISO)

circadian rhythm (ISO)

cognition (ISO)

collateral sprouting (IDA)

conditioned place preference (ISO)

dendrite development (ISO)

dendrite extension (ISO)

excitatory postsynaptic potential (ISO)

fear response (ISO)

feeding behavior (ISO)

gamma-aminobutyric acid signaling pathway (ISO)

glutamate secretion (ISO)

inhibitory postsynaptic potential (ISO)

inner ear development (ISO)

learning (ISO)

learning or memory (ISO)

mechanoreceptor differentiation (ISO)

mitochondrial electron transport, NADH to ubiquinone (ISO)

modulation of chemical synaptic transmission (IBA)

negative regulation of apoptotic process (ISO)

negative regulation of apoptotic signaling pathway (ISS)

negative regulation of myotube differentiation (ISS)

negative regulation of neuroblast proliferation (ISO)

negative regulation of neuron apoptotic process (IBA,ISO)

negative regulation of programmed cell death (ISO)

negative regulation of striated muscle tissue development (ISO)

negative regulation of synaptic transmission, GABAergic (ISO)

nerve development (IBA,ISO)

nerve growth factor signaling pathway (IBA)

nervous system development (ISO,TAS)

neuron apoptotic process (ISO)

neuron projection extension (ISO)

neuron projection morphogenesis (IBA)

neuron projection regeneration (ISO)

neuron recognition (ISO)

peptidyl-serine phosphorylation (ISO)

positive regulation of axon extension (ISO)

positive regulation of axon regeneration (ISO)

positive regulation of brain-derived neurotrophic factor receptor signaling pathway (TAS)

positive regulation of collateral sprouting (IDA,ISO)

positive regulation of DNA-binding transcription factor activity (ISO)

positive regulation of long-term neuronal synaptic plasticity (ISO)

positive regulation of neuron apoptotic process (ISO)

positive regulation of neuron differentiation (ISO)

positive regulation of neuron projection development (ISS)

positive regulation of nuclear receptor-mediated glucocorticoid signaling pathway (ISO)

positive regulation of peptidyl-serine phosphorylation (ISO)

positive regulation of synapse assembly (IDA)

regeneration (ISO)

regulation of axon extension (ISO)

regulation of collateral sprouting (ISO)

regulation of long-term neuronal synaptic plasticity (ISO)

regulation of neuron apoptotic process (ISO)

regulation of protein localization to cell surface (TAS)

regulation of retinal cell programmed cell death (ISO)

regulation of short-term neuronal synaptic plasticity (ISO)

regulation of synaptic plasticity (ISO)

response to activity (ISO)

response to anesthetic (ISO)

response to auditory stimulus (ISO)

response to electrical stimulus (ISO)

response to ethanol (ISO)

response to food (ISO)

response to hormone (ISO)

response to hyperoxia (ISO)

response to hypoxia (ISO)

response to L-glutamate (ISO)

response to light intensity (ISO)

response to light stimulus (ISO)

response to morphine (ISO)

response to nerve growth factor (ISO)

response to nutrient levels (ISO)

response to potassium ion (ISO)

response to tumor necrosis factor (ISO)

response to vitamin A (ISO)

response to xenobiotic stimulus (ISO)

signal transduction (IEA)

synapse assembly (IDA)

taste bud development (ISO)

trans-synaptic signaling by BDNF, modulating synaptic transmission (ISO)

ureteric bud development (ISO)

Cellular Component

axon (IBA,ISO)

cytoplasm (ISS)

cytoplasmic vesicle (ISO)

dendrite (IBA,ISO)

endoplasmic reticulum lumen (TAS)

extracellular region (IEA,TAS)

extracellular space (IBA,ISO)

glutamatergic synapse (ISO)

hippocampal mossy fiber to CA3 synapse (ISO)

membrane (IEA)

mitochondrial crista (ISO)

neuronal cell body (ISO)

neuronal dense core vesicle (ISO)

perikaryon (ISO)

perinuclear region of cytoplasm (ISS)

secretory granule (ISO)

synaptic vesicle (IBA,ISO)

terminal bouton (ISO)

Molecular Function

growth factor activity (IBA,IEA,TAS)

nerve growth factor receptor binding (IBA)

neurotrophin TRKB receptor binding (ISO)

protein binding (IPI)

signaling receptor binding (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

brain-derived neurotrophic factor signaling pathway (TAS)

Huntington's disease pathway (IEA)

mitogen activated protein kinase signaling pathway (IEA)

neurotrophic factor signaling pathway (IEA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Abnormality of the autonomic nervous system (IAGP)

Aganglionic megacolon (IAGP)

Ambiguous genitalia (IAGP)

Aplasia/Hypoplasia of the iris (IAGP)

Cataract (IAGP)

Cognitive impairment (IAGP)

Cryptorchidism (IAGP)

Displacement of the urethral meatus (IAGP)

Dysfunction of lateral corticospinal tracts (IAGP)

Everted lower lip vermilion (IAGP)

Ganglioneuroblastoma (IAGP)

Ganglioneuroma (IAGP)

Glaucoma (IAGP)

Hearing abnormality (IAGP)

Hypotonia (IAGP)

Intellectual disability (IAGP)

Lewy bodies (IAGP)

Mental deterioration (IAGP)

Microcephaly (IAGP)

Micrognathia (IAGP)

Neoplasm of the central nervous system (IAGP)

Neuroblastoma (IAGP)

Nystagmus (IAGP)

Obesity (IAGP)

Ptosis (IAGP)

Respiratory insufficiency (IAGP)

Scoliosis (IAGP)

Seizure (IAGP)

Short stature (IAGP)

Substantia nigra gliosis (IAGP)

Visual impairment (IAGP)

References

References - curated

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93.	Protective effect against ischemia and light damage of iris pigment epithelial cells transfected with the BDNF gene.	Kano T, etal., Invest Ophthalmol Vis Sci. 2002 Dec;43(12):3744-53.
94.	KEGG: Kyoto Encyclopedia of Genes and Genomes	KEGG
95.	Telmisartan protects against cognitive decline via up-regulation of brain-derived neurotrophic factor/tropomyosin-related kinase B in hippocampus of hypertensive rats.	Kishi T, etal., J Cardiol. 2012 Dec;60(6):489-94. doi: 10.1016/j.jjcc.2012.08.004. Epub 2012 Sep 2.
96.	Brain-derived neurotrophic factor (BDNF) and type 2 diabetes.	Krabbe KS, etal., Diabetologia. 2007 Feb;50(2):431-8. Epub 2006 Dec 7.
97.	BDNF mRNA expression is significantly upregulated in vestibular schwannomas and correlates with proliferative activity.	Kramer F, etal., J Neurooncol. 2010 May;98(1):31-9. doi: 10.1007/s11060-009-0063-6. Epub 2009 Nov 25.
98.	BDNF diminishes caspase-2 but not c-Jun immunoreactivity of neurons in retinal ganglion cell layer after transient ischemia.	Kurokawa T, etal., Invest Ophthalmol Vis Sci. 1999 Nov;40(12):3006-11.
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PMID:29339649	PMID:29345295	PMID:29350074	PMID:29357295	PMID:29357818	PMID:29369497	PMID:29402782	PMID:29402794	PMID:29409455	PMID:29414128	PMID:29432620	PMID:29446659
PMID:29449128	PMID:29466871	PMID:29480080	PMID:29482040	PMID:29499216	PMID:29499969	PMID:29506764	PMID:29512462	PMID:29516593	PMID:29525179	PMID:29539621	PMID:29550677
PMID:29573867	PMID:29579552	PMID:29584866	PMID:29590610	PMID:29595641	PMID:29615787	PMID:29649711	PMID:29661830	PMID:29680227	PMID:29705266	PMID:29734099	PMID:29734216
PMID:29748024	PMID:29759928	PMID:29775542	PMID:29785763	PMID:29799860	PMID:29802070	PMID:29842831	PMID:29856758	PMID:29858545	PMID:29859931	PMID:29865854	PMID:29934252
PMID:29935919	PMID:29938784	PMID:29944703	PMID:29952080	PMID:29973620	PMID:29992511	PMID:29997244	PMID:30008380	PMID:30015148	PMID:30017710	PMID:30017781	PMID:30021884
PMID:30039833	PMID:30067287	PMID:30076879	PMID:30078664	PMID:30118755	PMID:30129980	PMID:30133147	PMID:30134233	PMID:30134862	PMID:30134995	PMID:30135302	PMID:30140987
PMID:30143695	PMID:30149456	PMID:30150003	PMID:30150066	PMID:30181602	PMID:30242240	PMID:30258047	PMID:30259075	PMID:30269521	PMID:30274741	PMID:30280190	PMID:30285822
PMID:30308512	PMID:30309369	PMID:30321558	PMID:30322026	PMID:30329132	PMID:30335237	PMID:30347311	PMID:30352103	PMID:30363954	PMID:30375508	PMID:30376438	PMID:30382534
PMID:30387693	PMID:30388593	PMID:30402941	PMID:30418087	PMID:30428894	PMID:30448615	PMID:30448977	PMID:30449530	PMID:30456540	PMID:30472504	PMID:30519954	PMID:30522804
PMID:30526722	PMID:30550003	PMID:30575024	PMID:30575339	PMID:30586536	PMID:30586546	PMID:30590963	PMID:30616127	PMID:30616482	PMID:30617785	PMID:30622436	PMID:30640051
PMID:30641914	PMID:30644699	PMID:30659644	PMID:30664620	PMID:30670915	PMID:30674980	PMID:30677092	PMID:30695401	PMID:30710808	PMID:30711709	PMID:30771753	PMID:30775992
PMID:30776391	PMID:30794585	PMID:30826210	PMID:30831210	PMID:30833610	PMID:30855519	PMID:30875771	PMID:30882674	PMID:30887472	PMID:30897622	PMID:30899092	PMID:30901514
PMID:30904785	PMID:30909076	PMID:30909233	PMID:30952206	PMID:30965275	PMID:30967530	PMID:30981636	PMID:30988377	PMID:30991416	PMID:30992540	PMID:30994478	PMID:30998730
PMID:31004714	PMID:31010680	PMID:31041673	PMID:31057094	PMID:31059136	PMID:31071716	PMID:31083054	PMID:31089096	PMID:31098654	PMID:31100426	PMID:31102717	PMID:31104169
PMID:31112471	PMID:31132388	PMID:31134487	PMID:31172586	PMID:31180700	PMID:31197095	PMID:31202861	PMID:31208790	PMID:31210313	PMID:31234814	PMID:31247244	PMID:31255678
PMID:31255912	PMID:31255950	PMID:31257632	PMID:31291217	PMID:31291230	PMID:31295515	PMID:31298409	PMID:31317694	PMID:31349032	PMID:31364951	PMID:31365694	PMID:31379269
PMID:31420036	PMID:31425696	PMID:31437468	PMID:31445421	PMID:31453785	PMID:31464540	PMID:31465000	PMID:31487728	PMID:31495276	PMID:31502573	PMID:31524060	PMID:31541132
PMID:31556385	PMID:31560105	PMID:31571628	PMID:31573330	PMID:31601338	PMID:31617281	PMID:31623079	PMID:31636250	PMID:31642812	PMID:31661631	PMID:31688181	PMID:31711978
PMID:31713782	PMID:31736231	PMID:31746551	PMID:31756156	PMID:31760580	PMID:31767813	PMID:31771052	PMID:31820346	PMID:31839607	PMID:31845634	PMID:31900428	PMID:31910296
PMID:31925827	PMID:31926908	PMID:31941116	PMID:31951637	PMID:32002751	PMID:32009534	PMID:32010924	PMID:32012942	PMID:32015336	PMID:32056765	PMID:32056943	PMID:32065946
PMID:32066722	PMID:32075548	PMID:32077707	PMID:32079998	PMID:32080982	PMID:32081932	PMID:32085670	PMID:32085720	PMID:32122804	PMID:32124075	PMID:32157099	PMID:32171272
PMID:32204647	PMID:32210348	PMID:32246495	PMID:32291635	PMID:32296183	PMID:32327658	PMID:32349267	PMID:32350920	PMID:32351633	PMID:32358323	PMID:32361384	PMID:32378476
PMID:32390303	PMID:32397876	PMID:32416472	PMID:32423492	PMID:32428748	PMID:32482330	PMID:32492978	PMID:32562379	PMID:32565776	PMID:32570881	PMID:32573858	PMID:32605421
PMID:32612070	PMID:32629065	PMID:32638952	PMID:32654287	PMID:32664008	PMID:32679912	PMID:32686489	PMID:32696315	PMID:32703621	PMID:32724091	PMID:32726665	PMID:32731218
PMID:32736598	PMID:32759658	PMID:32798619	PMID:32804326	PMID:32808327	PMID:32810467	PMID:32813897	PMID:32814053	PMID:32815193	PMID:32819178	PMID:32848137	PMID:32859253
PMID:32869548	PMID:32892314	PMID:32911446	PMID:32931807	PMID:32933711	PMID:32941187	PMID:32949664	PMID:32983417	PMID:32985495	PMID:32988741	PMID:32991522	PMID:32996114
PMID:33002731	PMID:33004884	PMID:33007373	PMID:33015172	PMID:33029116	PMID:33036942	PMID:33044176	PMID:33047388	PMID:33047489	PMID:33050457	PMID:33053385	PMID:33060610
PMID:33063528	PMID:33068389	PMID:33073590	PMID:33077716	PMID:33087740	PMID:33096634	PMID:33105359	PMID:33160139	PMID:33173426	PMID:33179143	PMID:33182716	PMID:33215284
PMID:33215785	PMID:33222311	PMID:33222669	PMID:33253827	PMID:33271690	PMID:33288548	PMID:33302387	PMID:33306590	PMID:33306691	PMID:33315318	PMID:33324399	PMID:33325388
PMID:33338736	PMID:33340609	PMID:33358916	PMID:33358963	PMID:33360223	PMID:33369083	PMID:33370585	PMID:33389140	PMID:33389158	PMID:33405375	PMID:33413076	PMID:33434621
PMID:33441099	PMID:33444650	PMID:33450468	PMID:33477654	PMID:33479229	PMID:33485990	PMID:33499851	PMID:33523719	PMID:33561695	PMID:33568689	PMID:33574220	PMID:33578508
PMID:33603039	PMID:33605167	PMID:33628340	PMID:33637225	PMID:33660804	PMID:33662047	PMID:33666096	PMID:33721459	PMID:33749030	PMID:33753004	PMID:33757426	PMID:33762638
PMID:33773278	PMID:33773809	PMID:33787399	PMID:33798614	PMID:33812160	PMID:33835731	PMID:33857523	PMID:33862146	PMID:33876571	PMID:33878808	PMID:33883635	PMID:33910384
PMID:33926045	PMID:33930460	PMID:33942699	PMID:33957818	PMID:33961781	PMID:33971247	PMID:33985854	PMID:33993081	PMID:34000980	PMID:34008409	PMID:34053675	PMID:34160912
PMID:34173192	PMID:34175359	PMID:34176754	PMID:34209215	PMID:34209365	PMID:34215825	PMID:34245319	PMID:34248009	PMID:34256395	PMID:34258927	PMID:34263656	PMID:34263997
PMID:34267235	PMID:34281873	PMID:34321412	PMID:34340176	PMID:34341419	PMID:34346275	PMID:34359010	PMID:34367374	PMID:34415897	PMID:34418703	PMID:34418778	PMID:34425486
PMID:34445512	PMID:34467592	PMID:34478125	PMID:34518555	PMID:34525971	PMID:34528295	PMID:34533795	PMID:34536433	PMID:34537904	PMID:34546355	PMID:34573321	PMID:34580389
PMID:34591410	PMID:34592560	PMID:34601245	PMID:34602450	PMID:34610834	PMID:34625629	PMID:34637871	PMID:34650209	PMID:34653830	PMID:34653961	PMID:34654737	PMID:34750906
PMID:34757248	PMID:34760029	PMID:34763683	PMID:34788141	PMID:34856753	PMID:34879183	PMID:34896179	PMID:34936818	PMID:34954335	PMID:34965503	PMID:34974714	PMID:34989854
PMID:34990638	PMID:34991456	PMID:34997117	PMID:35009001	PMID:35023483	PMID:35077325	PMID:35099506	PMID:35121746	PMID:35128618	PMID:35129860	PMID:35152066	PMID:35165396
PMID:35205376	PMID:35206257	PMID:35208502	PMID:35219096	PMID:35228136	PMID:35292247	PMID:35295960	PMID:35300713	PMID:35314247	PMID:35328036	PMID:35349796	PMID:35354697
PMID:35364229	PMID:35378105	PMID:35451419	PMID:35453068	PMID:35459929	PMID:35465864	PMID:35486119	PMID:35489561	PMID:35508633	PMID:35599479	PMID:35605794	PMID:35633348
PMID:35662115	PMID:35666604	PMID:35679772	PMID:35696571	PMID:35717586	PMID:35718045	PMID:35718064	PMID:35728773	PMID:35743044	PMID:35748555	PMID:35749045	PMID:35809326
PMID:35866837	PMID:35886019	PMID:35887357	PMID:35905107	PMID:35905264	PMID:35905690	PMID:35918221	PMID:35927806	PMID:35947418	PMID:35962006	PMID:35970042	PMID:35988269
PMID:35998179	PMID:36108429	PMID:36114161	PMID:36115874	PMID:36168703	PMID:36173064	PMID:36181754	PMID:36214902	PMID:36223549	PMID:36268760	PMID:36329115	PMID:36336706
PMID:36355087	PMID:36367618	PMID:36394751	PMID:36398374	PMID:36411369	PMID:36438922	PMID:36441149	PMID:36453692	PMID:36481244	PMID:36498925	PMID:36510348	PMID:36528281
PMID:36550387	PMID:36563920	PMID:36567420	PMID:36577338	PMID:36597258	PMID:36621163	PMID:36630045	PMID:36681359	PMID:36682419	PMID:36719088	PMID:36737401	PMID:36739005
PMID:36764636	PMID:36766691	PMID:36780947	PMID:36787304	PMID:36794980	PMID:36800691	PMID:36834953	PMID:36835126	PMID:36855816	PMID:36884028	PMID:36898188	PMID:36950384
PMID:36970903	PMID:36977737	PMID:36999446	PMID:37019247	PMID:37038358	PMID:37072879	PMID:37075935	PMID:37076286	PMID:37085692	PMID:37094390	PMID:37146499	PMID:37150680
PMID:37175781	PMID:37182424	PMID:37186275	PMID:37220696	PMID:37230202	PMID:37252844	PMID:37257214	PMID:37315256	PMID:37334438	PMID:37334527	PMID:37334646	PMID:37335428
PMID:37358362	PMID:37387382	PMID:37404130	PMID:37460933	PMID:37462904	PMID:37491857	PMID:37508514	PMID:37520481	PMID:37522679	PMID:37548699	PMID:37596403	PMID:37675625
PMID:37692110	PMID:37703265	PMID:37706246	PMID:37759825	PMID:37770565	PMID:37820958	PMID:37865417	PMID:37871642	PMID:37944291	PMID:38006577	PMID:38008209	PMID:38009531
PMID:38063117	PMID:38070471	PMID:38110605	PMID:38114721	PMID:38127937	PMID:38136952	PMID:38142902	PMID:38148427	PMID:38151886	PMID:38164567	PMID:38218833	PMID:38228888
PMID:38243072	PMID:38245698	PMID:38254671	PMID:38255861	PMID:38261293	PMID:38279143	PMID:38331308	PMID:38338875	PMID:38379321	PMID:38385466	PMID:38397427	PMID:38417539
PMID:38447916	PMID:38454193	PMID:38503023	PMID:38542252	PMID:38554393	PMID:38564888	PMID:38677095	PMID:38706964	PMID:38720004	PMID:38726479	PMID:38749085	PMID:38788070
PMID:38791290	PMID:38861537	PMID:38982490	PMID:38988190	PMID:39334009	PMID:39392027

Genomics

Comparative Map Data

BDNF
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	27,654,893 - 27,722,030 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	27,654,893 - 27,722,058 (-)	Ensembl			hg38	GRCh38
GRCh37	11	27,676,440 - 27,743,577 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	27,633,016 - 27,699,872 (-)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	11	27,633,019 - 27,637,249	NCBI
Celera	11	27,822,548 - 27,889,725 (-)	NCBI		Celera
Cytogenetic Map	11	p14.1	NCBI
HuRef	11	27,374,586 - 27,441,772 (-)	NCBI		HuRef
CHM1_1	11	27,675,184 - 27,742,527 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	27,795,301 - 27,862,460 (-)	NCBI		T2T-CHM13v2.0

Bdnf
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	109,505,045 - 109,557,388 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	109,505,045 - 109,557,352 (+)	Ensembl		GRCm39 Ensembl		GRCm39
GRCm38	2	109,674,700 - 109,727,043 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	109,674,700 - 109,727,007 (+)	Ensembl			mm10	GRCm38
MGSCv37	2	109,514,857 - 109,567,200 (+)	NCBI	MGSCv37	MGSCv37	mm9	NCBIm37
MGSCv36	2	109,475,539 - 109,527,845 (+)	NCBI		MGSCv36	mm8
Celera	2	110,835,441 - 110,887,723 (+)	NCBI		Celera
Cytogenetic Map	2	E3	NCBI
cM Map	2	56.63	NCBI

Bdnf
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	116,619,633 - 116,670,212 (+)	NCBI	GRCr8	GRCr8		GRCr8
GRCr8 Ensembl	3	116,619,633 - 116,670,657 (+)	Ensembl				GRCr8
mRatBN7.2	3	96,165,042 - 96,215,621 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	96,165,042 - 96,215,615 (+)	Ensembl				mRatBN7.2
UTH_Rnor_SHR_Utx	3	99,726,226 - 99,776,801 (+)	NCBI	UTH_Rnor_SHR_Utx	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	108,325,184 - 108,375,759 (+)	NCBI	UTH_Rnor_SHRSP_BbbUtx_1.0	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	106,087,694 - 106,138,272 (+)	NCBI	UTH_Rnor_WKY_Bbb_1.0	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	100,768,637 - 100,819,216 (+)	NCBI	Rnor_6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	100,768,637 - 100,819,210 (+)	Ensembl			rn6	Rnor6.0
Rnor_5.0	3	107,371,329 - 107,421,908 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
Celera	3	95,191,318 - 95,241,949 (+)	NCBI		Celera
Cytogenetic Map	3	q34	NCBI

Bdnf
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955476	6,772,088 - 6,822,588 (-)	Ensembl
ChiLan1.0	NW_004955476	6,773,244 - 6,822,201 (-)	NCBI	ChiLan1.0	ChiLan1.0

BDNF
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	29,867,082 - 29,934,015 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	29,867,593 - 29,934,527 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	27,618,322 - 27,687,661 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	27,520,306 - 27,589,239 (-)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	27,520,312 - 27,589,239 (-)	Ensembl			panPan2	panpan1.1

BDNF
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	21	48,191,580 - 48,243,699 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	21	48,192,670 - 48,204,480 (-)	Ensembl			canFam3	CanFam3.1
Dog10K_Boxer_Tasha	21	47,689,871 - 47,691,000 (-)	NCBI	Dog10K_Boxer_Tasha	Dog10K_Boxer_Tasha
ROS_Cfam_1.0	21	49,335,793 - 49,386,964 (-)	NCBI	ROS_Cfam_1.0	ROS_Cfam_1.0
UMICH_Zoey_3.1	21	48,338,131 - 48,339,260 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	21	48,489,388 - 48,490,517 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	21	49,083,467 - 49,084,596 (-)	NCBI	UU_Cfam_GSD_1.0	UU_Cfam_GSD_1.0

Bdnf
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	36,374,992 - 36,427,979 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936540	5,529,942 - 5,585,014 (+)	Ensembl		SpeTri2.0 Ensembl
SpeTri2.0	NW_004936540	5,530,081 - 5,582,765 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

BDNF
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	32,624,048 - 32,679,765 (+)	Ensembl			susScr11	Sscrofa11.1
Sscrofa11.1	2	32,623,668 - 32,679,293 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	35,206,996 - 35,265,002 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

BDNF
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	37,386,825 - 37,451,380 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	37,449,593 - 37,450,336 (+)	Ensembl		ChlSab1.1 Ensembl	chlSab2	Vervet-AGM
Vero_WHO_p1.0	NW_023666038	134,690,869 - 134,762,531 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Bdnf
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624766	17,279,630 - 17,330,490 (-)	Ensembl		HetGla_female_1.0 Ensembl	hetGla2	HetGla_female_1.0 Ensembl
HetGla 1.0	NW_004624766	17,281,882 - 17,330,601 (-)	NCBI	HetGla 1.0	HetGla 1.0	hetGla2

Variants

Variants in BDNF
154 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_001709.5(BDNF):c.-46C>T	single nucleotide variant	Variant of unknown significance [RCV000019273]	Chr11:27700188 [GRCh38] Chr11:27721735 [GRCh37] Chr11:11p14.1	pathogenic\|uncertain significance
NM_001709.5(BDNF):c.5C>T (p.Thr2Ile)	single nucleotide variant	BDNF-related disorder [RCV003914855]\|Congenital central hypoventilation [RCV000019266]\|Obesity [RCV000988510]\|not provided [RCV002513118]\|not specified [RCV000790920]	Chr11:27658560 [GRCh38] Chr11:27680107 [GRCh37] Chr11:11p14.1	pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance
NM_001709.5(BDNF):c.196G>A (p.Val66Met)	single nucleotide variant	Memory impairment, susceptibility to [RCV000019267]\|not provided [RCV002054446]\|not specified [RCV000155463]	Chr11:27658369 [GRCh38] Chr11:27679916 [GRCh37] Chr11:11p14.1	risk factor\|association\|benign\|protective\|not provided
GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1	copy number loss	See cases [RCV000052648]	Chr11:22550115..38199159 [GRCh38] Chr11:22571661..38220709 [GRCh37] Chr11:22528237..38177285 [NCBI36] Chr11:11p14.3-12	pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3	copy number gain	See cases [RCV000053613]	Chr11:202758..31726224 [GRCh38] Chr11:202758..31747772 [GRCh37] Chr11:192758..31704348 [NCBI36] Chr11:11p15.5-13	pathogenic
NM_170731.4(BDNF):c.103C>T (p.Arg35Ter)	single nucleotide variant	Malignant melanoma [RCV000069311]	Chr11:27658486 [GRCh38] Chr11:27680033 [GRCh37] Chr11:27636609 [NCBI36] Chr11:11p14.1	not provided
GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1	copy number loss	See cases [RCV000135295]	Chr11:26368962..35252976 [GRCh38] Chr11:26390509..35274523 [GRCh37] Chr11:26347085..35231099 [NCBI36] Chr11:11p14.2-13	pathogenic
GRCh38/hg38 11p14.3-13(chr11:24595399-31096539)x3	copy number gain	See cases [RCV000134877]	Chr11:24595399..31096539 [GRCh38] Chr11:24616945..31118086 [GRCh37] Chr11:24573521..31074662 [NCBI36] Chr11:11p14.3-13	pathogenic
GRCh38/hg38 11p14.3-14.1(chr11:23024064-27978597)x1	copy number loss	See cases [RCV000137723]	Chr11:23024064..27978597 [GRCh38] Chr11:23045610..28000144 [GRCh37] Chr11:23002186..27956720 [NCBI36] Chr11:11p14.3-14.1	likely pathogenic
GRCh38/hg38 11p15.1-13(chr11:20079474-34463996)x1	copy number loss	See cases [RCV000142499]	Chr11:20079474..34463996 [GRCh38] Chr11:20101020..34485543 [GRCh37] Chr11:20057596..34442119 [NCBI36] Chr11:11p15.1-13	pathogenic
NM_001709.5(BDNF):c.-22+774G>A	single nucleotide variant	not provided [RCV004718045]\|not specified [RCV000150189]	Chr11:27699390 [GRCh38] Chr11:27720937 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.450= (p.Ala150=)	single nucleotide variant	not provided [RCV002056111]\|not specified [RCV000156118]	Chr11:27658115 [GRCh38] Chr11:27679662 [GRCh37] Chr11:11p14.1	benign
GRCh37/hg19 11p14.1(chr11:27407012-28000144)x3	copy number gain	See cases [RCV000240429]	Chr11:27407012..28000144 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.502G>T (p.Glu168Ter)	single nucleotide variant	Inborn genetic diseases [RCV000622995]	Chr11:27658063 [GRCh38] Chr11:27679610 [GRCh37] Chr11:11p14.1	likely pathogenic
NM_001709.5(BDNF):c.-21-15685_-21-15684del	deletion	not specified [RCV000595956]	Chr11:27674269..27674270 [GRCh38] Chr11:27695816..27695817 [GRCh37] Chr11:11p14.1	uncertain significance
GRCh37/hg19 11p15.1-13(chr11:18536224-31923308)x1	copy number loss	Aniridia 1 [RCV000420782]	Chr11:18536224..31923308 [GRCh37] Chr11:11p15.1-13	pathogenic
GRCh37/hg19 11p15.1-13(chr11:21586131-33168232)x1	copy number loss	Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome [RCV000435400]	Chr11:21586131..33168232 [GRCh37] Chr11:11p15.1-13	pathogenic
GRCh37/hg19 11p14.2-11.12(chr11:26574629-50508019)x3	copy number gain	See cases [RCV000448603]	Chr11:26574629..50508019 [GRCh37] Chr11:11p14.2-11.12	pathogenic
GRCh37/hg19 11p14.3-13(chr11:25771208-35614978)x1	copy number loss	See cases [RCV000512014]	Chr11:25771208..35614978 [GRCh37] Chr11:11p14.3-13	pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3	copy number gain	See cases [RCV000511561]	Chr11:230615..37698540 [GRCh37] Chr11:11p15.5-12	pathogenic
GRCh37/hg19 11p14.1-12(chr11:27588560-41770792)x1	copy number loss	See cases [RCV000511434]	Chr11:27588560..41770792 [GRCh37] Chr11:11p14.1-12	pathogenic\|uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_001709.5(BDNF):c.-22+764G>C	single nucleotide variant	not specified [RCV000601884]	Chr11:27699400 [GRCh38] Chr11:27720947 [GRCh37] Chr11:11p14.1	uncertain significance
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3	copy number gain	See cases [RCV000512477]	Chr11:230615..31995219 [GRCh37] Chr11:11p15.5-13	pathogenic
GRCh37/hg19 11p14.3-14.1(chr11:25090108-28909131)x3	copy number gain	not provided [RCV000683363]	Chr11:25090108..28909131 [GRCh37] Chr11:11p14.3-14.1	uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p14.3-12(chr11:24469451-37524085)x1	copy number loss	not provided [RCV000737457]	Chr11:24469451..37524085 [GRCh37] Chr11:11p14.3-12	pathogenic
GRCh37/hg19 11p14.3-13(chr11:25196998-34196484)x1	copy number loss	not provided [RCV000737466]	Chr11:25196998..34196484 [GRCh37] Chr11:11p14.3-13	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p14.2-13(chr11:27154853-33302474)x1	copy number loss	not provided [RCV000749997]	Chr11:27154853..33302474 [GRCh37] Chr11:11p14.2-13	pathogenic
NM_001709.5(BDNF):c.483C>A (p.Gly161=)	single nucleotide variant	not provided [RCV000976679]	Chr11:27658082 [GRCh38] Chr11:27679629 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15633G>A	single nucleotide variant	Obesity [RCV000754971]	Chr11:27674218 [GRCh38] Chr11:27695765 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.546C>T (p.Tyr182=)	single nucleotide variant	BDNF-related disorder [RCV003940507]\|not provided [RCV000884732]	Chr11:27658019 [GRCh38] Chr11:27679566 [GRCh37] Chr11:11p14.1	benign\|likely benign
NM_001709.5(BDNF):c.642C>T (p.Tyr214=)	single nucleotide variant	not provided [RCV000951291]	Chr11:27657923 [GRCh38] Chr11:27679470 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.417C>T (p.Ser139=)	single nucleotide variant	BDNF-related disorder [RCV004746124]\|not provided [RCV000881363]	Chr11:27658148 [GRCh38] Chr11:27679695 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.450G>A (p.Ala150=)	single nucleotide variant	not provided [RCV000964612]\|not specified [RCV004017766]	Chr11:27658115 [GRCh38] Chr11:27679662 [GRCh37] Chr11:11p14.1	benign
GRCh37/hg19 11p15.3-13(chr11:11053978-34732891)x3	copy number gain	not provided [RCV001006387]	Chr11:11053978..34732891 [GRCh37] Chr11:11p15.3-13	pathogenic
NM_001709.5(BDNF):c.639G>A (p.Ser213=)	single nucleotide variant	not provided [RCV000891648]	Chr11:27657926 [GRCh38] Chr11:27679473 [GRCh37] Chr11:11p14.1	benign
GRCh37/hg19 11p14.3-13(chr11:22079154-35597645)x1	copy number loss	not provided [RCV000849589]	Chr11:22079154..35597645 [GRCh37] Chr11:11p14.3-13	pathogenic
NM_001709.5(BDNF):c.136G>A (p.Val46Met)	single nucleotide variant	BDNF-related disorder [RCV003393061]\|not provided [RCV003778321]	Chr11:27658429 [GRCh38] Chr11:27679976 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15653T>C	single nucleotide variant	not specified [RCV001699686]	Chr11:27674238 [GRCh38] Chr11:27695785 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-15332T>C	single nucleotide variant	not provided [RCV001639767]	Chr11:27673917 [GRCh38] Chr11:27695464 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.483C>T (p.Gly161=)	single nucleotide variant	BDNF-related disorder [RCV003902990]\|not provided [RCV000920255]	Chr11:27658082 [GRCh38] Chr11:27679629 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.321C>G (p.Leu107=)	single nucleotide variant	not provided [RCV000911836]	Chr11:27658244 [GRCh38] Chr11:27679791 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-15601_-21-15600del	deletion	BDNF-related disorder [RCV003401662]\|not provided [RCV001730262]	Chr11:27674185..27674186 [GRCh38] Chr11:27695732..27695733 [GRCh37] Chr11:11p14.1	likely benign\|uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3	copy number gain	not provided [RCV001006372]	Chr11:235934..33826995 [GRCh37] Chr11:11p15.5-13	pathogenic
NM_001709.5(BDNF):c.-21-1064CA[11]	microsatellite	not provided [RCV001669309]	Chr11:27659629..27659630 [GRCh38] Chr11:27681176..27681177 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-1044G>C	single nucleotide variant	not provided [RCV001669145]	Chr11:27659629 [GRCh38] Chr11:27681176 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.557G>A (p.Cys186Tyr)	single nucleotide variant	Obesity [RCV001261409]	Chr11:27658008 [GRCh38] Chr11:27679555 [GRCh37] Chr11:11p14.1	likely pathogenic
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
NM_001143808.2(BDNF):c.-22+2T>G	single nucleotide variant	BDNF-related disorder [RCV003928861]\|not provided [RCV001357477]	Chr11:27700979 [GRCh38] Chr11:27722526 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-1256G>A	single nucleotide variant	not provided [RCV001708958]	Chr11:27659841 [GRCh38] Chr11:27681388 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-1064CA[13]	microsatellite	not provided [RCV001615493]	Chr11:27659629..27659630 [GRCh38] Chr11:27681176..27681177 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-15778G>T	single nucleotide variant	not provided [RCV001687535]	Chr11:27674363 [GRCh38] Chr11:27695910 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-15304=	single nucleotide variant	not provided [RCV001711020]	Chr11:27673889 [GRCh38] Chr11:27695436 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.-21-1065G>A	single nucleotide variant	not provided [RCV001708763]	Chr11:27659650 [GRCh38] Chr11:27681197 [GRCh37] Chr11:11p14.1	benign
NM_001709.5(BDNF):c.643G>A (p.Val215Met)	single nucleotide variant	not provided [RCV001726839]	Chr11:27657922 [GRCh38] Chr11:27679469 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.542T>G (p.Phe181Cys)	single nucleotide variant	Inherited obesity [RCV004818543]	Chr11:27658023 [GRCh38] Chr11:27679570 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.273G>A (p.Thr91=)	single nucleotide variant	BDNF-related disorder [RCV003913612]\|not provided [RCV002219957]	Chr11:27658292 [GRCh38] Chr11:27679839 [GRCh37] Chr11:11p14.1	likely benign
GRCh37/hg19 11p14.1-13(chr11:27547893-31656604)x1	copy number loss	not provided [RCV002265529]	Chr11:27547893..31656604 [GRCh37] Chr11:11p14.1-13	not provided
GRCh37/hg19 11p14.1(chr11:27382897-29172035)x1	copy number loss	See cases [RCV002292391]	Chr11:27382897..29172035 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.170C>A (p.Thr57Lys)	single nucleotide variant	Inborn genetic diseases [RCV002840034]	Chr11:27658395 [GRCh38] Chr11:27679942 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.128T>C (p.Leu43Pro)	single nucleotide variant	Inborn genetic diseases [RCV002839678]	Chr11:27658437 [GRCh38] Chr11:27679984 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.366G>T (p.Met122Ile)	single nucleotide variant	not provided [RCV002815720]	Chr11:27658199 [GRCh38] Chr11:27679746 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.70G>A (p.Ala24Thr)	single nucleotide variant	Inborn genetic diseases [RCV002836785]	Chr11:27658495 [GRCh38] Chr11:27680042 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.609T>C (p.His203=)	single nucleotide variant	not provided [RCV002928085]	Chr11:27657956 [GRCh38] Chr11:27679503 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.233G>A (p.Arg78Gln)	single nucleotide variant	BDNF-related disorder [RCV004747243]\|Inborn genetic diseases [RCV002798325]	Chr11:27658332 [GRCh38] Chr11:27679879 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.447G>A (p.Thr149=)	single nucleotide variant	BDNF-related disorder [RCV003928910]\|Inborn genetic diseases [RCV002887297]\|not provided [RCV003738324]	Chr11:27658118 [GRCh38] Chr11:27679665 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.164G>T (p.Gly55Val)	single nucleotide variant	Inborn genetic diseases [RCV002782083]	Chr11:27658401 [GRCh38] Chr11:27679948 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.323T>A (p.Phe108Tyr)	single nucleotide variant	not provided [RCV002735121]	Chr11:27658242 [GRCh38] Chr11:27679789 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.223C>G (p.Gln75Glu)	single nucleotide variant	BDNF-related disorder [RCV003420539]\|Inborn genetic diseases [RCV002805148]	Chr11:27658342 [GRCh38] Chr11:27679889 [GRCh37] Chr11:11p14.1	likely benign\|uncertain significance
NM_001709.5(BDNF):c.184A>G (p.Thr62Ala)	single nucleotide variant	Inborn genetic diseases [RCV002831186]	Chr11:27658381 [GRCh38] Chr11:27679928 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.49A>G (p.Lys17Glu)	single nucleotide variant	not provided [RCV003008479]	Chr11:27658516 [GRCh38] Chr11:27680063 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001143809.2(BDNF):c.49G>A (p.Ala17Thr)	single nucleotide variant	BDNF-related disorder [RCV003419127]	Chr11:27700988 [GRCh38] Chr11:27722535 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15487T>G	single nucleotide variant	BDNF-related disorder [RCV003419162]	Chr11:27674072 [GRCh38] Chr11:27695619 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.365T>C (p.Met122Thr)	single nucleotide variant	BDNF-related disorder [RCV003412001]	Chr11:27658200 [GRCh38] Chr11:27679747 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15496C>G	single nucleotide variant	BDNF-related disorder [RCV003392770]	Chr11:27674081 [GRCh38] Chr11:27695628 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.5C>A (p.Thr2Asn)	single nucleotide variant	BDNF-related disorder [RCV003404640]	Chr11:27658560 [GRCh38] Chr11:27680107 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15533T>C	single nucleotide variant	BDNF-related disorder [RCV003391508]	Chr11:27674118 [GRCh38] Chr11:27695665 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.92G>A (p.Gly31Asp)	single nucleotide variant	BDNF-related disorder [RCV003408713]	Chr11:27658473 [GRCh38] Chr11:27680020 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.659T>C (p.Met220Thr)	single nucleotide variant	BDNF-related disorder [RCV003412440]	Chr11:27657906 [GRCh38] Chr11:27679453 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15481C>A	single nucleotide variant	BDNF-related disorder [RCV003405951]	Chr11:27674066 [GRCh38] Chr11:27695613 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.226A>G (p.Lys76Glu)	single nucleotide variant	BDNF-related disorder [RCV003399548]	Chr11:27658339 [GRCh38] Chr11:27679886 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15659_-21-15656dup	duplication	BDNF-related disorder [RCV003417130]	Chr11:27674240..27674241 [GRCh38] Chr11:27695787..27695788 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.691A>G (p.Ile231Val)	single nucleotide variant	BDNF-related disorder [RCV003410856]	Chr11:27657874 [GRCh38] Chr11:27679421 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.113G>A (p.Arg38Gln)	single nucleotide variant	BDNF-related disorder [RCV003417144]	Chr11:27658452 [GRCh38] Chr11:27679999 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.72A>G (p.Ala24=)	single nucleotide variant	not provided [RCV003692609]	Chr11:27658493 [GRCh38] Chr11:27680040 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.172T>C (p.Ser58Pro)	single nucleotide variant	not provided [RCV003822313]	Chr11:27658393 [GRCh38] Chr11:27679940 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.610del (p.Trp204fs)	deletion	not provided [RCV003719409]	Chr11:27657955 [GRCh38] Chr11:27679502 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.258C>T (p.Asp86=)	single nucleotide variant	BDNF-related disorder [RCV003939123]\|Inborn genetic diseases [RCV005301319]\|not provided [RCV003564868]	Chr11:27658307 [GRCh38] Chr11:27679854 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.135C>T (p.Ser45=)	single nucleotide variant	BDNF-related disorder [RCV003977379]	Chr11:27658430 [GRCh38] Chr11:27679977 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.102C>T (p.Tyr34=)	single nucleotide variant	BDNF-related disorder [RCV003894003]	Chr11:27658463 [GRCh38] Chr11:27680010 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.239A>G (p.Asn80Ser)	single nucleotide variant	BDNF-related disorder [RCV003979549]	Chr11:27658326 [GRCh38] Chr11:27679873 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001143809.2(BDNF):c.39G>C (p.Lys13Asn)	single nucleotide variant	BDNF-related disorder [RCV003956950]	Chr11:27700998 [GRCh38] Chr11:27722545 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.195C>T (p.His65=)	single nucleotide variant	BDNF-related disorder [RCV003981835]	Chr11:27658370 [GRCh38] Chr11:27679917 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.154G>A (p.Gly52Ser)	single nucleotide variant	BDNF-related disorder [RCV003957003]	Chr11:27658411 [GRCh38] Chr11:27679958 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15592C>T	single nucleotide variant	BDNF-related disorder [RCV003899378]	Chr11:27674177 [GRCh38] Chr11:27695724 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15571A>G	single nucleotide variant	BDNF-related disorder [RCV003951854]	Chr11:27674156 [GRCh38] Chr11:27695703 [GRCh37] Chr11:11p14.1	likely benign
NM_001143809.2(BDNF):c.66+8T>C	single nucleotide variant	BDNF-related disorder [RCV003941878]	Chr11:27700963 [GRCh38] Chr11:27722510 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15601A>G	single nucleotide variant	BDNF-related disorder [RCV003907203]	Chr11:27674186 [GRCh38] Chr11:27695733 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.309G>A (p.Glu103=)	single nucleotide variant	BDNF-related disorder [RCV003934389]	Chr11:27658256 [GRCh38] Chr11:27679803 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.480G>A (p.Ser160=)	single nucleotide variant	BDNF-related disorder [RCV003924661]	Chr11:27658085 [GRCh38] Chr11:27679632 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15610G>A	single nucleotide variant	BDNF-related disorder [RCV003943953]	Chr11:27674195 [GRCh38] Chr11:27695742 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.465T>C (p.Thr155=)	single nucleotide variant	BDNF-related disorder [RCV003901373]	Chr11:27658100 [GRCh38] Chr11:27679647 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.241G>T (p.Glu81Ter)	single nucleotide variant	not provided [RCV004575952]	Chr11:27658324 [GRCh38] Chr11:27679871 [GRCh37] Chr11:11p14.1	uncertain significance
NC_000011.9:g.(?_27528379)_(27744859_?)del	deletion	not provided [RCV004580377]	Chr11:27528379..27744859 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.101A>G (p.Tyr34Cys)	single nucleotide variant	Inborn genetic diseases [RCV004600128]	Chr11:27658464 [GRCh38] Chr11:27680011 [GRCh37] Chr11:11p14.1	uncertain significance
NM_170731.5(BDNF):c.3+20368T>C	single nucleotide variant	BDNF-related disorder [RCV004745785]	Chr11:27701044 [GRCh38] Chr11:27722591 [GRCh37] Chr11:11p14.1	likely benign
NM_001143809.2(BDNF):c.28C>T (p.Arg10Cys)	single nucleotide variant	BDNF-related disorder [RCV004745869]	Chr11:27701009 [GRCh38] Chr11:27722556 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.630T>C (p.Thr210=)	single nucleotide variant	BDNF-related disorder [RCV004746059]	Chr11:27657935 [GRCh38] Chr11:27679482 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15688C>T	single nucleotide variant	BDNF-related disorder [RCV004746789]	Chr11:27674273 [GRCh38] Chr11:27695820 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.226A>C (p.Lys76Gln)	single nucleotide variant	BDNF-related disorder [RCV004726510]	Chr11:27658339 [GRCh38] Chr11:27679886 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15591G>A	single nucleotide variant	BDNF-related disorder [RCV004746635]	Chr11:27674176 [GRCh38] Chr11:27695723 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15634T>C	single nucleotide variant	BDNF-related disorder [RCV004746688]	Chr11:27674219 [GRCh38] Chr11:27695766 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15529C>T	single nucleotide variant	BDNF-related disorder [RCV004747594]	Chr11:27674114 [GRCh38] Chr11:27695661 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.466G>A (p.Ala156Thr)	single nucleotide variant	BDNF-related disorder [RCV004726654]	Chr11:27658099 [GRCh38] Chr11:27679646 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.15C>T (p.Phe5=)	single nucleotide variant	BDNF-related disorder [RCV004747884]	Chr11:27658550 [GRCh38] Chr11:27680097 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.508G>A (p.Val170Ile)	single nucleotide variant	BDNF-related disorder [RCV004746708]	Chr11:27658057 [GRCh38] Chr11:27679604 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.*9T>C	single nucleotide variant	BDNF-related disorder [RCV004746825]	Chr11:27657812 [GRCh38] Chr11:27679359 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.463A>T (p.Thr155Ser)	single nucleotide variant	BDNF-related disorder [RCV004747003]	Chr11:27658102 [GRCh38] Chr11:27679649 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001143809.2(BDNF):c.63G>A (p.Gly21=)	single nucleotide variant	BDNF-related disorder [RCV004747955]	Chr11:27700974 [GRCh38] Chr11:27722521 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15623A>C	single nucleotide variant	BDNF-related disorder [RCV004747583]	Chr11:27674208 [GRCh38] Chr11:27695755 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001143809.2(BDNF):c.53G>A (p.Gly18Glu)	single nucleotide variant	BDNF-related disorder [RCV004748000]	Chr11:27700984 [GRCh38] Chr11:27722531 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15523C>T	single nucleotide variant	BDNF-related disorder [RCV004745736]	Chr11:27674108 [GRCh38] Chr11:27695655 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.735G>A (p.Arg245=)	single nucleotide variant	BDNF-related disorder [RCV004745715]	Chr11:27657830 [GRCh38] Chr11:27679377 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.111G>A (p.Val37=)	single nucleotide variant	BDNF-related disorder [RCV004745765]	Chr11:27658454 [GRCh38] Chr11:27680001 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.190G>A (p.Glu64Lys)	single nucleotide variant	BDNF-related disorder [RCV004745959]	Chr11:27658375 [GRCh38] Chr11:27679922 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15556A>G	single nucleotide variant	BDNF-related disorder [RCV004747581]	Chr11:27674141 [GRCh38] Chr11:27695688 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.563C>G (p.Pro188Arg)	single nucleotide variant	BDNF-related disorder [RCV004747611]	Chr11:27658002 [GRCh38] Chr11:27679549 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.360A>G (p.Ala120=)	single nucleotide variant	BDNF-related disorder [RCV004747766]	Chr11:27658205 [GRCh38] Chr11:27679752 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.633C>A (p.Thr211=)	single nucleotide variant	BDNF-related disorder [RCV004729963]	Chr11:27657932 [GRCh38] Chr11:27679479 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.495A>T (p.Thr165=)	single nucleotide variant	BDNF-related disorder [RCV004747993]	Chr11:27658070 [GRCh38] Chr11:27679617 [GRCh37] Chr11:11p14.1	likely benign
NM_001143809.2(BDNF):c.2T>C (p.Met1Thr)	single nucleotide variant	BDNF-related disorder [RCV004747848]	Chr11:27701035 [GRCh38] Chr11:27722582 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.715T>G (p.Cys239Gly)	single nucleotide variant	BDNF-related disorder [RCV004729666]	Chr11:27657850 [GRCh38] Chr11:27679397 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.81A>C (p.Arg27=)	single nucleotide variant	BDNF-related disorder [RCV004745677]	Chr11:27658484 [GRCh38] Chr11:27680031 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.*4A>G	single nucleotide variant	BDNF-related disorder [RCV004745704]	Chr11:27657817 [GRCh38] Chr11:27679364 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.534G>A (p.Lys178=)	single nucleotide variant	BDNF-related disorder [RCV004745730]	Chr11:27658031 [GRCh38] Chr11:27679578 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.721T>C (p.Leu241=)	single nucleotide variant	BDNF-related disorder [RCV004746111]	Chr11:27657844 [GRCh38] Chr11:27679391 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.114G>T (p.Arg38=)	single nucleotide variant	BDNF-related disorder [RCV004746992]	Chr11:27658451 [GRCh38] Chr11:27679998 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.280G>A (p.Val94Met)	single nucleotide variant	BDNF-related disorder [RCV004747783]	Chr11:27658285 [GRCh38] Chr11:27679832 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15625A>G	single nucleotide variant	BDNF-related disorder [RCV004724278]	Chr11:27674210 [GRCh38] Chr11:27695757 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.638C>T (p.Ser213Leu)	single nucleotide variant	BDNF-related disorder [RCV004746101]	Chr11:27657927 [GRCh38] Chr11:27679474 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.36C>A (p.Tyr12Ter)	single nucleotide variant	BDNF-related disorder [RCV004746707]	Chr11:27658529 [GRCh38] Chr11:27680076 [GRCh37] Chr11:11p14.1	uncertain significance
NM_170731.5(BDNF):c.3+20367A>G	single nucleotide variant	BDNF-related disorder [RCV004746685]	Chr11:27701045 [GRCh38] Chr11:27722592 [GRCh37] Chr11:11p14.1	likely benign
NM_001143809.2(BDNF):c.39G>A (p.Lys13=)	single nucleotide variant	BDNF-related disorder [RCV004747787]	Chr11:27700998 [GRCh38] Chr11:27722545 [GRCh37] Chr11:11p14.1	likely benign
NM_001143809.2(BDNF):c.28C>A (p.Arg10Ser)	single nucleotide variant	BDNF-related disorder [RCV004745742]	Chr11:27701009 [GRCh38] Chr11:27722556 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.488C>T (p.Thr163Met)	single nucleotide variant	BDNF-related disorder [RCV004745679]	Chr11:27658077 [GRCh38] Chr11:27679624 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.272C>A (p.Thr91Lys)	single nucleotide variant	BDNF-related disorder [RCV004745820]	Chr11:27658293 [GRCh38] Chr11:27679840 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.418G>A (p.Val140Met)	single nucleotide variant	BDNF-related disorder [RCV004745856]	Chr11:27658147 [GRCh38] Chr11:27679694 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15635C>T	single nucleotide variant	BDNF-related disorder [RCV004746032]	Chr11:27674220 [GRCh38] Chr11:27695767 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.489G>A (p.Thr163=)	single nucleotide variant	BDNF-related disorder [RCV004746053]	Chr11:27658076 [GRCh38] Chr11:27679623 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-21-15541C>A	single nucleotide variant	BDNF-related disorder [RCV004746712]	Chr11:27674126 [GRCh38] Chr11:27695673 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-22+764G>A	single nucleotide variant	BDNF-related disorder [RCV004747564]	Chr11:27699400 [GRCh38] Chr11:27720947 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.547G>A (p.Glu183Lys)	single nucleotide variant	BDNF-related disorder [RCV004747804]	Chr11:27658018 [GRCh38] Chr11:27679565 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.-21-15602C>T	single nucleotide variant	BDNF-related disorder [RCV004747876]	Chr11:27674187 [GRCh38] Chr11:27695734 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.537A>G (p.Gln179=)	single nucleotide variant	BDNF-related disorder [RCV004747866]	Chr11:27658028 [GRCh38] Chr11:27679575 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.-22+777G>T	single nucleotide variant	BDNF-related disorder [RCV004724323]	Chr11:27699387 [GRCh38] Chr11:27720934 [GRCh37] Chr11:11p14.1	uncertain significance
GRCh37/hg19 11p14.3-13(chr11:24192701-32455527)x1	copy number loss	not provided [RCV004819368]	Chr11:24192701..32455527 [GRCh37] Chr11:11p14.3-13	pathogenic
NM_001709.5(BDNF):c.163G>A (p.Gly55Ser)	single nucleotide variant	Inborn genetic diseases [RCV004969897]	Chr11:27658402 [GRCh38] Chr11:27679949 [GRCh37] Chr11:11p14.1	uncertain significance
GRCh37/hg19 11p14.3-12(chr11:22428384-37196643)x1	copy number loss	not provided [RCV004819367]	Chr11:22428384..37196643 [GRCh37] Chr11:11p14.3-12	pathogenic
NM_001709.5(BDNF):c.370A>T (p.Met124Leu)	single nucleotide variant	Inborn genetic diseases [RCV004969895]	Chr11:27658195 [GRCh38] Chr11:27679742 [GRCh37] Chr11:11p14.1	uncertain significance
GRCh37/hg19 11p15.1-12(chr11:17120358-41424289)x1	copy number loss	not provided [RCV004819366]	Chr11:17120358..41424289 [GRCh37] Chr11:11p15.1-12	pathogenic
NM_001709.5(BDNF):c.75C>T (p.Asn25=)	single nucleotide variant	not provided [RCV005069730]	Chr11:27658490 [GRCh38] Chr11:27680037 [GRCh37] Chr11:11p14.1	likely benign
NM_001709.5(BDNF):c.293G>A (p.Ser98Asn)	single nucleotide variant	Inborn genetic diseases [RCV005314318]	Chr11:27658272 [GRCh38] Chr11:27679819 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.331G>C (p.Glu111Gln)	single nucleotide variant	Inborn genetic diseases [RCV005305802]	Chr11:27658234 [GRCh38] Chr11:27679781 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.221A>C (p.Asp74Ala)	single nucleotide variant	Inborn genetic diseases [RCV005305805]	Chr11:27658344 [GRCh38] Chr11:27679891 [GRCh37] Chr11:11p14.1	uncertain significance
NM_001709.5(BDNF):c.321C>T (p.Leu107=)	single nucleotide variant	Inborn genetic diseases [RCV005305806]	Chr11:27658244 [GRCh38] Chr11:27679791 [GRCh37] Chr11:11p14.1	likely benign

miRNA Target Status (No longer updated)

Confirmed Target Of

miRNA Gene	Mature miRNA	Method Name	Result Type	Data Type	Support Type	PMID
MIR30A	hsa-miR-30a-3p	Mirecords	external_info	NA	NA	18632683
MIR1-1	hsa-miR-1	Mirtarbase	external_info	Luciferase reporter assay	Functional MTI	14697198
MIR22	hsa-miR-22-3p	Mirtarbase	external_info	Luciferase reporter assay//Microarray	Functional MTI	21168126
MIR204	hsa-miR-204-5p	OncomiRDB	external_info	NA	NA	23285024

Predicted Target Of

	Summary Value
Count of predictions:	25467
Count of miRNA genes:	1169
Interacting mature miRNAs:	1532
Transcripts:	ENST00000314915, ENST00000356660, ENST00000395978, ENST00000395980, ENST00000395981, ENST00000395983, ENST00000395986, ENST00000418212, ENST00000420794, ENST00000438929, ENST00000439476, ENST00000525528, ENST00000525950, ENST00000530786, ENST00000530861, ENST00000532997, ENST00000533131, ENST00000533246, ENST00000584049
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597504797	GWAS1600871_H	triglyceride measurement QTL GWAS1600871 (human)		3e-10	triglyceride amount (VT:0000187)	blood triglyceride level (CMO:0000118)	11	27673288	27673289	Human
1576345	LVC1_H	Left ventricular contractility QTL 1 (human)	3.93		Left ventricular contractility		11	7970767	33970767	Human
2289313	BW388_H	Body weight QTL 388 (human)	1.57	0.00356	Body fat amount	abdominal	11	4434671	30434671	Human
597336729	GWAS1432803_H	C-reactive protein measurement QTL GWAS1432803 (human)		2e-24	C-reactive protein amount (VT:0010036)	blood C-reactive protein level (CMO:0003160)	11	27678578	27678579	Human
597064850	GWAS1160924_H	body mass index QTL GWAS1160924 (human)		0.000005	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
597232030	GWAS1328104_H	smoking cessation QTL GWAS1328104 (human)		0.000003	smoking cessation		11	27672694	27672695	Human
596955932	GWAS1075451_H	inflammatory biomarker measurement, diet measurement QTL GWAS1075451 (human)		9e-12	inflammatory biomarker measurement, diet measurement		11	27680836	27680837	Human
597383186	GWAS1479260_H	age at menarche QTL GWAS1479260 (human)		9e-16	estrous cycle trait (VT:0001927)		11	27680836	27680837	Human
597041052	GWAS1137126_H	snoring measurement QTL GWAS1137126 (human)		0.000004	sleep behavior trait (VT:0001501)		11	27672694	27672695	Human
597486486	GWAS1582560_H	body mass index QTL GWAS1582560 (human)		7e-63	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27682662	27682663	Human
597438993	GWAS1535067_H	body mass index QTL GWAS1535067 (human)		1e-34	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27680836	27680837	Human
597030811	GWAS1126885_H	smoking initiation QTL GWAS1126885 (human)		1e-11	behavior trait (VT:0010442)		11	27672694	27672695	Human
406891217	GWAS540193_H	body mass index QTL GWAS540193 (human)		7e-10	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
597493000	GWAS1589074_H	body mass index QTL GWAS1589074 (human)		9e-09	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27656036	27656037	Human
596987148	GWAS1106667_H	body mass index QTL GWAS1106667 (human)		6e-15	body mass index		11	27656039	27656040	Human
597065612	GWAS1161686_H	body mass index QTL GWAS1161686 (human)		1e-12	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
597241219	GWAS1337293_H	C-reactive protein measurement QTL GWAS1337293 (human)		1e-18	C-reactive protein amount (VT:0010036)	blood C-reactive protein level (CMO:0003160)	11	27678578	27678579	Human
596987145	GWAS1106664_H	fat body mass QTL GWAS1106664 (human)		1e-08	fat body mass		11	27656039	27656040	Human
407163992	GWAS812968_H	age at menarche QTL GWAS812968 (human)		3e-11	estrous cycle trait (VT:0001927)		11	27678578	27678579	Human
597411463	GWAS1507537_H	age at menopause QTL GWAS1507537 (human)		0.0000002	estrous cycle trait (VT:0001927)		11	27680836	27680837	Human
406890974	GWAS539950_H	body mass index QTL GWAS539950 (human)		8e-42	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
596966065	GWAS1085584_H	body mass index QTL GWAS1085584 (human)		2e-50	body mass index		11	27712873	27712874	Human
597065788	GWAS1161862_H	physical activity measurement, body mass index QTL GWAS1161862 (human)		2e-22	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27678578	27678579	Human
407125871	GWAS774847_H	snoring measurement QTL GWAS774847 (human)		9e-11	sleep behavior trait (VT:0001501)		11	27672694	27672695	Human
597064743	GWAS1160817_H	body mass index QTL GWAS1160817 (human)		1e-11	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27678578	27678579	Human
597504937	GWAS1601011_H	COVID-19, obesity QTL GWAS1601011 (human)		8e-14	eating behavior trait (VT:0001431)		11	27680836	27680837	Human
596960800	GWAS1080319_H	metabolic syndrome QTL GWAS1080319 (human)		5e-54	metabolic syndrome		11	27690834	27690835	Human
597501098	GWAS1597172_H	triglyceride measurement QTL GWAS1597172 (human)		1e-11	triglyceride amount (VT:0000187)	blood triglyceride level (CMO:0000118)	11	27673288	27673289	Human
597339173	GWAS1435247_H	puberty onset measurement QTL GWAS1435247 (human)		1e-10	time of sexual maturation trait (VT:0001938)		11	27672694	27672695	Human
596968663	GWAS1088182_H	body mass index QTL GWAS1088182 (human)		9e-51	body mass index		11	27658369	27658370	Human
597066964	GWAS1163038_H	age at menarche QTL GWAS1163038 (human)		0.0000001	estrous cycle trait (VT:0001927)		11	27678578	27678579	Human
597392350	GWAS1488424_H	triglyceride measurement QTL GWAS1488424 (human)		9e-13	triglyceride amount (VT:0000187)	blood triglyceride level (CMO:0000118)	11	27673288	27673289	Human
597399388	GWAS1495462_H	uric acid measurement QTL GWAS1495462 (human)		2e-08	blood uric acid amount (VT:0010302)	blood uric acid level (CMO:0000501)	11	27672444	27672445	Human
597467861	GWAS1563935_H	feeling nervous measurement QTL GWAS1563935 (human)		3e-09	emotion/affect behavior trait (VT:0002572)		11	27673288	27673289	Human
597064902	GWAS1160976_H	body mass index QTL GWAS1160976 (human)		3e-10	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
1559107	SCL32_H	Serum cholesterol level QTL 32 (human)	3.27		Lipid level	LDL cholesterol	11	2892430	28892430	Human
597284172	GWAS1380246_H	C-reactive protein measurement QTL GWAS1380246 (human)		4e-12	C-reactive protein amount (VT:0010036)	blood C-reactive protein level (CMO:0003160)	11	27672694	27672695	Human
597064896	GWAS1160970_H	physical activity measurement, body mass index QTL GWAS1160970 (human)		0.000001	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
1559104	SCL15_H	Serum cholesterol level QTL 15 (human)	2.6	0.06	Lipid level	hyperlipidemia susceptibility	11	15892368	41892368	Human
596963278	GWAS1082797_H	fat body mass QTL GWAS1082797 (human)		1e-32	fat body mass		11	27690834	27690835	Human
1559113	SCL31_H	Serum cholesterol level QTL 31 (human)	3.72		Lipid level	LDL cholesterol	11	2892430	28892430	Human
597041225	GWAS1137299_H	snoring measurement QTL GWAS1137299 (human)		9e-10	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27672694	27672695	Human
597500670	GWAS1596744_H	body weight QTL GWAS1596744 (human)		1e-11	body mass (VT:0001259)	body weight (CMO:0000012)	11	27656036	27656037	Human
597368831	GWAS1464905_H	hematocrit QTL GWAS1464905 (human)		1e-10	erythrocyte morphology trait (VT:0002447)	hematocrit (CMO:0000037)	11	27656036	27656037	Human
596963315	GWAS1082834_H	body mass index QTL GWAS1082834 (human)		1e-37	body mass index		11	27690834	27690835	Human
597366003	GWAS1462077_H	hemoglobin measurement QTL GWAS1462077 (human)		1e-09	blood hemoglobin amount (VT:0001588)	hemoglobin measurement (CMO:0000508)	11	27656036	27656037	Human
597614068	GWAS1670928_H	sodium measurement QTL GWAS1670928 (human)		2e-13	blood sodium amount (VT:0001776)	blood sodium level (CMO:0000499)	11	27672694	27672695	Human
597065468	GWAS1161542_H	physical activity measurement, body mass index QTL GWAS1161542 (human)		2e-19	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27678578	27678579	Human
596989669	GWAS1109188_H	body mass index QTL GWAS1109188 (human)		3e-27	body mass index		11	27712873	27712874	Human
596989668	GWAS1109187_H	body mass index QTL GWAS1109187 (human)		4e-56	body mass index		11	27658369	27658370	Human
597064288	GWAS1160362_H	physical activity measurement, body mass index QTL GWAS1160362 (human)		2e-21	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27678578	27678579	Human
597015907	GWAS1111981_H	coronary artery disease QTL GWAS1111981 (human)		0.000003	coronary artery integrity trait (VT:0010746)		11	27680836	27680837	Human
597427307	GWAS1523381_H	urate measurement QTL GWAS1523381 (human)		2e-11	urate measurement	blood uric acid level (CMO:0000501)	11	27672444	27672445	Human
596953069	GWAS1072588_H	body mass index QTL GWAS1072588 (human)		2e-36	body mass index		11	27709009	27709010	Human
597522150	GWAS1618224_H	urate measurement QTL GWAS1618224 (human)		2e-08	urate measurement	blood uric acid level (CMO:0000501)	11	27673288	27673289	Human
597064941	GWAS1161015_H	body mass index QTL GWAS1161015 (human)		3e-15	body size trait (VT:0100005)	body mass index (BMI) (CMO:0000105)	11	27678578	27678579	Human
596964456	GWAS1083975_H	body mass index QTL GWAS1083975 (human)		1e-28	body mass index		11	27656039	27656040	Human
597224676	GWAS1320750_H	C-reactive protein measurement QTL GWAS1320750 (human)		2e-11	C-reactive protein amount (VT:0010036)	blood C-reactive protein level (CMO:0003160)	11	27672694	27672695	Human
597455584	GWAS1551658_H	inflammatory biomarker measurement, diet measurement QTL GWAS1551658 (human)		9e-12	eating behavior trait (VT:0001431)	food intake measurement (CMO:0000772)	11	27680836	27680837	Human
407038525	GWAS687501_H	risk-taking behaviour QTL GWAS687501 (human)		3e-11	exploratory behavior trait (VT:0010471)		11	27672694	27672695	Human

Markers in Region

D11S4115

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,737,913 - 27,738,101	UniSTS	GRCh37
Build 36	11	27,694,489 - 27,694,677	RGD	NCBI36
Celera	11	27,884,027 - 27,884,221	RGD
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,436,072 - 27,436,264	UniSTS
Marshfield Genetic Map	11	35.21	RGD
Marshfield Genetic Map	11	35.21	UniSTS
Genethon Genetic Map	11	38.7	UniSTS
deCODE Assembly Map	11	44.48	UniSTS
Whitehead-YAC Contig Map	11		UniSTS

D11S1270

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,730,319 - 27,730,713	UniSTS	GRCh37
Build 36	11	27,686,895 - 27,687,289	RGD	NCBI36
Celera	11	27,876,432 - 27,876,827	RGD
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,428,479 - 27,428,874	UniSTS

D11S2825

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,709,227 - 27,709,393	UniSTS	GRCh37
Build 36	11	27,665,803 - 27,665,969	RGD	NCBI36
Celera	11	27,855,336 - 27,855,502	RGD
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,407,388 - 27,407,554	UniSTS

GDB:197571

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,680,022 - 27,680,600	UniSTS	GRCh37
Build 36	11	27,636,598 - 27,637,176	RGD	NCBI36
Celera	11	27,826,129 - 27,826,707	RGD
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,378,167 - 27,378,745	UniSTS

BDNF

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,681,064 - 27,681,285	UniSTS	GRCh37
GRCh37	11	27,679,498 - 27,680,106	UniSTS	GRCh37
Build 36	11	27,637,640 - 27,637,861	RGD	NCBI36
Celera	11	27,825,605 - 27,826,213	UniSTS
Celera	11	27,827,171 - 27,827,394	RGD
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,379,209 - 27,379,432	UniSTS
HuRef	11	27,377,643 - 27,378,251	UniSTS
GeneMap99-GB4 RH Map	11	106.12	UniSTS

BDNF-1

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,679,473 - 27,679,755	UniSTS	GRCh37
Build 36	11	27,636,049 - 27,636,331	RGD	NCBI36
Celera	11	27,825,580 - 27,825,862	RGD
HuRef	11	27,377,618 - 27,377,900	UniSTS

BDNF_2411

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,678,808 - 27,679,691	UniSTS	GRCh37
Build 36	11	27,635,384 - 27,636,267	RGD	NCBI36
Celera	11	27,824,916 - 27,825,798	RGD
HuRef	11	27,376,954 - 27,377,836	UniSTS

D11S4429

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	27,679,106 - 27,679,207	UniSTS	GRCh37
Build 36	11	27,635,682 - 27,635,783	RGD	NCBI36
Celera	11	27,825,213 - 27,825,314	RGD
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	11	p13	UniSTS
HuRef	11	27,377,251 - 27,377,352	UniSTS
Whitehead-YAC Contig Map	11		UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1199	2382	2746	2226	4934	1631	2234	4	533	1288	375	2252	6450	5789	39	3708	826	1724	1589	171

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_011794	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143805	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143806	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143808	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143809	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001143816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_170731	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_170732	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_170733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_170734	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_170735	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011520280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB038670	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB038671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB038672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB038673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB038674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC103796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104563	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF400438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF411339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289763	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289853	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY011481	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054392	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054395	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054396	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054397	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054398	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054399	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054400	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY054406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY442188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY656701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC029795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CX751420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ250642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF674517	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF674518	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF674519	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF674520	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF674521	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689009	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689010	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689012	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689013	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689016	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689017	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689018	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689019	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF689021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HM763820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KC855559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF455346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KP229412	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU177943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU177944	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KU177945	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KX964616	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KX964617	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M37762	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M61176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M61181	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X60201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X60202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X91251	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000314915 ⟹ ENSP00000320002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,722,058 (-)	Ensembl

Ensembl Acc Id:

ENST00000356660 ⟹ ENSP00000349084

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,700,455 (-)	Ensembl

Ensembl Acc Id:

ENST00000395978 ⟹ ENSP00000379302

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,720,723 (-)	Ensembl

Ensembl Acc Id:

ENST00000395980 ⟹ ENSP00000379304

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,633 (-)	Ensembl

Ensembl Acc Id:

ENST00000395981 ⟹ ENSP00000379305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,720,723 (-)	Ensembl

Ensembl Acc Id:

ENST00000395983 ⟹ ENSP00000379307

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,053 (-)	Ensembl

Ensembl Acc Id:

ENST00000395986 ⟹ ENSP00000379309

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,699,667 (-)	Ensembl

Ensembl Acc Id:

ENST00000418212 ⟹ ENSP00000400502

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,700,488 (-)	Ensembl

Ensembl Acc Id:

ENST00000420794 ⟹ ENSP00000389564

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,053 (-)	Ensembl

Ensembl Acc Id:

ENST00000438929 ⟹ ENSP00000414303

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,053 (-)	Ensembl

Ensembl Acc Id:

ENST00000439476 ⟹ ENSP00000389345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,659,658 (-)	Ensembl

Ensembl Acc Id:

ENST00000525528 ⟹ ENSP00000437138

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,659,658 (-)	Ensembl

Ensembl Acc Id:

ENST00000525950 ⟹ ENSP00000432035

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,720,779 (-)	Ensembl

Ensembl Acc Id:

ENST00000530786 ⟹ ENSP00000433003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,053 (-)	Ensembl

Ensembl Acc Id:

ENST00000530861 ⟹ ENSP00000435564

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,700,900 (-)	Ensembl

Ensembl Acc Id:

ENST00000532997 ⟹ ENSP00000435805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,719,747 (-)	Ensembl

Ensembl Acc Id:

ENST00000533131 ⟹ ENSP00000432727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,699,667 (-)	Ensembl

Ensembl Acc Id:

ENST00000533246 ⟹ ENSP00000432376

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,700,488 (-)	Ensembl

Ensembl Acc Id:

ENST00000584049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	27,654,893 - 27,701,633 (-)	Ensembl

RefSeq Acc Id:

NM_001143805 ⟹ NP_001137277

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,720,779 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,741,249 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,861,210 (-)	NCBI

Sequence:

show sequence

AATATCAAGTATCACTTAATTAGAGATTTTTAAGCCTTTTCCTCCTGCTGTGCCGGGTGTGTAA
TCCGGGCGATAGGAGTCCATTCAGCACCTTGGACAGAGCCAACGGATTTGTCCGAGGTGGCGGT
ACCCCCAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATA
CTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCC
TACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAG
GCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAA
AGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGT
AGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATG
CTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGT
GTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGC
GGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACG
AGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTG
GAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGA
ATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAA
GATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTGTATATAT
ACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAA
GTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACA
GTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCG
TTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTG
AATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAACACACACACACACAACAAAAATT
TGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATC
TGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCAT
TGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTT
CGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATA
TATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATG
ACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGA
TGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGG
ACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTT
TTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACAC
ATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAA
CAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCAT
GGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCC
TGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAA
CAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGA
GTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCC
TCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTT
TAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGA
CTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTG
GGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCT
GAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGT
AAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGG
AAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAG
GTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCA
CAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTG
GGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAA
AACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGA
CCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAG
CAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTT
CAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGA
CTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATA
TGTAAGGAATGCTTGGAATATCTGCTATATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAA
TTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGT
TTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCAC
AGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTG
TTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGT
GTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAA
TGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATAT
TTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACC
GCATCAGAACCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGTT
TTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143806 ⟹ NP_001137278

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,720,779 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,741,249 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,861,210 (-)	NCBI

Sequence:

show sequence

AATATCAAGTATCACTTAATTAGAGATTTTTAAGCCTTTTCCTCCTGCTGTGCCGGGTGTGTAA
TCCGGGCGATAGGAGTCCATTCAGCACCTTGGACAGAGCCAACGGATTTGTCCGAGGTGGCGGT
ACCCCCAGGTAGTCTTCTTGGCCCCGCTGTAAAGCCAACCCTGTGTCGCCCTTAAAAAGCGTCT
TTTCTGAGGTTCGGCTCACACTGAGATCGGGGCTGGAGAGAGAGTCAGATTTTGGAGCGGAGCG
TTTGGAAAGCGAGCCCCAGTTTGGTCCCCTCATTGAGCTCGCTGAAGTTGGCTTCCTAGCGGTG
TAGGCTGGAATAGACTCTTGGCAAGCTCCGGTTCCACCAGGTGAGAAGAGTGATGACCATCCTT
TTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACA
TCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAA
TGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAA
GAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGT
ACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGA
GGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCT
GCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAA
AGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGG
CCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGC
AGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCC
TTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATG
TACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGAC
AAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTT
TATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACA
TGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTT
GATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATA
AATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAA
CACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATC
TTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAA
CAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTT
TTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAG
ATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAG
ATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAA
TGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAG
AGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCC
TCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTAC
CACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAG
TGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAG
GAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGT
CTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCAC
ATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACC
GGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATT
TGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGT
CAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGA
CTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAA
TTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAAT
GAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGG
TTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCC
GAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGAC
ATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAA
ATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTC
CCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCT
TGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAA
AATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGC
ATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCA
TCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGA
ATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATAT
TATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTATATGTCAACTTTAT
GCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGC
AAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTC
TTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTT
TGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGC
TGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGA
TTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCA
CCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAA
AAAATTGGCATTAAAACTTAACCGCATCAGAACCTATTGTAAATACAAGTTCTATTTAAGTGTA
CTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAA
GTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143807 ⟹ NP_001137279

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,719,566 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,740,217 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,859,997 (-)	NCBI

Sequence:

show sequence

AGCTGCCGAGACCGCGCTCCGCTCCCCAGCCGGGCCGGATGCCTCACTGAGCCCAGTTCCACCA
GGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAG
GCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGA
CCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGC
TGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAA
GAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGG
AGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCAT
GAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGT
GAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCC
TTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCC
CATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGA
ACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCA
TAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGT
TGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAAT
TATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGT
GGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAAC
TTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAA
ACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTG
TCCTCTTTCAGAAAACAGAAAAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTC
CGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTT
AACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTA
GGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTG
TTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGAT
AAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATA
AAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCC
CCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCA
GAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAAT
CAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCAT
GACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACC
CCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAA
AAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAA
ACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGC
TATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGG
TCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTC
AGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTA
TCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATC
CCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGC
ATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTT
TGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAAC
AGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAG
ACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATG
GAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCC
CATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCA
AGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAG
CCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGT
ATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTC
ACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAG
AGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAG
ATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTG
GAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAAC
CCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACA
TCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGAT
GGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTG
TTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCA
GCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGT
TCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGT
ATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTAT
TGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATT
TTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143808 ⟹ NP_001137280

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,701,053 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,721,513 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,841,478 (-)	NCBI

Sequence:

show sequence

GTAAACCAATAGCCCCCATGCTCTGTGCGATTTCATTGTGTGCTCGCGTTCGCAAGCTCCGTAG
TGCAGGAAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCAT
ACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGC
CTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGA
GGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGA
AAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAG
TAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGAT
GCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCG
TGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGG
CGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTAC
GAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATT
GGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAG
AATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGA
AGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTGTATATA
TACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGA
AGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAAC
AGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCC
GTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGT
GAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACACACAACAAAAA
TTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATA
TCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTC
ATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTT
TTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAA
TATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGA
TGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGT
GATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAA
GGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTG
TTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAAC
ACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAA
AACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATC
ATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGC
CCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTG
AACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCT
GAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGG
CCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGC
TTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCC
GACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGT
TGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTAC
CTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTG
GTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATA
GGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGA
AGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGC
CACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTT
TGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTG
AAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTG
GACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATA
AGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTG
TTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAA
GACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAA
TATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACA
AATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTG
GTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATC
ACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTG
TGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAA
GTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTA
AATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAAT
ATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAA
CCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATAATATAT
GTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143809 ⟹ NP_001137281

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,701,053 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,721,513 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,841,478 (-)	NCBI

Sequence:

show sequence

GTAAACCAATAGCCCCCATGCTCTGTGCGATTTCATTGTGTGCTCGCGTTCGCAAGCTCCGTAG
TGCAGGAAGGTGCGGGAAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATG
GTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAG
GTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGC
AGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGAT
GAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGG
TGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAA
TTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGG
GAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGG
ACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCA
ATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGAC
AAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATA
GCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCAT
TAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTA
TTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCAT
GTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCA
GAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTG
GTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTG
CTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACAC
ACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGT
TAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGG
TGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTT
GTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGA
ATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAAT
ATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTC
CACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCT
TTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCT
CTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGA
ACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTT
TAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATT
TGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAA
AAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGA
CATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGG
AGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCC
AAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTG
GACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCA
CACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCC
TGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGA
TGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTG
AGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAG
GGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACAC
CAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCC
CAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACC
TCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGG
ATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGA
TCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGG
GTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAA
TTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTG
AAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAA
TTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTT
TTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGAT
CTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAAT
AAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCT
CTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTT
TGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAA
AATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAAC
AAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCAT
TAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACA
TATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143810 ⟹ NP_001137282

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,701,053 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,721,513 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,841,478 (-)	NCBI

Sequence:

show sequence

GTAAACCAATAGCCCCCATGCTCTGTGCGATTTCATTGTGTGCTCGCGTTCGCAAGCTCCGTAG
TGCAGGAAGGTGCGGGAAGTTAAGTAATTAAAAGAAATTATAGAGTGGGATGCAAAAATAACCC
GAAGGACAACTGGATGTGTGGAGCCACCAGTTTTCTCCATGAGTGCACAAGGTTAATCCTTGTT
ACTACTCAGAATGCTGAGTTTCTACAGAAAGGGTTGCAGGTCCACACATGTTTTGGCGTCTACC
CACACGCTTCTGTATGGCATGACTGTGCATCCCAGAAGAAGGGCTGTGCTGTGTACCTCCACGT
TTCAGTGGAATTTAACAAACTGATCCCTGAAAATGGTTTCATAAAGTTCCACCAGGTGAGAAGA
GTGATGACCATCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCA
TGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGAC
TCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTC
GAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATA
AGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCT
TCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGG
CGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAA
CGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGT
CCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTAC
ACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGT
CGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGA
CACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATT
AGATTATATTGAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTA
AGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAA
TCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTC
TGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAG
TTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCA
GAAAACAGAAAAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATT
TTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGAT
AGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGG
GATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTT
CCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACA
TTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGG
CAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTC
TTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTC
TTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCG
TTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTA
TAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAA
GATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGG
TGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGAT
CAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGT
TGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGA
GGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCT
CTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTG
CTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGG
ATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATC
ATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGA
CTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAA
ACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTC
GGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCA
GGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCT
GTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGC
CTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGC
CCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGC
CCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCC
AGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTT
TCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTG
TGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGC
TGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCAC
AAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATT
GTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTT
GACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTG
TTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGT
TGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATG
GTAAAGATATTATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATAT
AATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACA
AGTTCTATTTAAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTT
TTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143811 ⟹ NP_001137283

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,701,053 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,721,513 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,841,478 (-)	NCBI

Sequence:

show sequence

GTAAACCAATAGCCCCCATGCTCTGTGCGATTTCATTGTGTGCTCGCGTTCGCAAGCTCCGTAG
TGCAGGAAGGTGCGGGAAGTTAAGTAATTAAAAGAAATTATAGAGTGGGATGCAAAAATAACCC
GAAGGACAACTGGATGTGTGGAGCCACCAGTTTTCTCCATGAGTGCACAAGGTTAATCCTTGTT
ACTACTCAGAATGCTGAGTTTCTACAGAAAGGGTTGCAGGTCCACACATGTTTTGGCGTCTACC
CACACGCTTCTGTATGGCATGACTGTGCATCCCAGAAGAAGGGCTGTGCTGTGTACCTCCACGT
TTCAGTGGAATTTAACAAACTGATCCCTGAAAATGGTTTCATAAAGGGATGGTAATAAAGTCTC
TTAGTGGTTGAAAATGTTATTTCTTACAAAAGTGGAGAACATTTGCTTTTCAATACCAGAGTTT
TCAGCCATTTCTGCATTCTGACCTATTGACTGGAGTTCCACCAGGTGAGAAGAGTGATGACCAT
CCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCA
AACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCG
TGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGAT
AGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGAC
TTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGC
TGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGA
CCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGAC
AAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAA
AAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGG
CTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGG
GCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTG
TATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTG
AGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATA
ATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTG
GACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATT
CCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAAT
AATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAA
AAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAA
GTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAAT
TAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTA
TATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAG
TAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTG
TGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAA
AAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTG
GTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCT
CCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATAT
TTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAG
AACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTT
ATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAAC
AATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAA
TCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCAT
TTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATG
GTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACA
TGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTT
CTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCA
TAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGAT
GCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAAC
CAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTC
AGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTC
TGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTG
ACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGA
GGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTG
GTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACAC
CTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATT
GCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGA
TACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCA
TCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAA
AATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAAC
TTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGG
ATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGT
GGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATT
TATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGT
CTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTAT
GGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATT
ATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTAT
TGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTA
AGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATT
TTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143812 ⟹ NP_001137284

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,700,900 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,721,360 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,841,325 (-)	NCBI

Sequence:

show sequence

AGAGTTGAAAGCTAGGGGAGCGAGACCTCGGGGCGTGCGATTCTCACTCGCTCCCTCCCGCCCC
AGCGCCCACAGCCGGGGTTTCTGCAGAGGGCGCGGGACGCGGGGTTCCCCGGGGCTGAGGCTGG
GGCTGGAACACCCCTCGAAGCCGCGGGCGTCCTGTCCAAGGCGCCCCAGGAGGGCGCAGGACTC
GCAGGGCGATGTCGCGGGGCCCTAGGGGAGGAGTTCCACCAGGTGAGAAGAGTGATGACCATCC
TTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAA
CATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTG
AATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAG
AAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTT
GTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTG
GAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACC
CTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAA
AAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAA
GGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCT
GCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGC
CCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTA
TGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAG
ACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAAT
TTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGA
CATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCC
TTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAA
TAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAA
AAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGT
ATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTA
AAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATA
TTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTA
GAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTG
AAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAA
AAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGT
CAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCC
CCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTT
TACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAA
CAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTAT
GAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAA
TGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATC
CACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTT
ACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGT
ATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATG
TGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCT
CGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATA
AAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGC
AATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCA
GGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAG
GCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTG
GACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGAC
AAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGG
GTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGT
TCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCT
GAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGC
TGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATA
CCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATC
TGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAA
TATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTT
TATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGAT
TGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGG
CTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTA
TTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCT
TGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGG
CGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTAT
TCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTG
AAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAG
TGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTT
CAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143813 ⟹ NP_001137285

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,700,455 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,720,774 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,840,883 (-)	NCBI

Sequence:

show sequence

GCAGCCTGGAGCTCCGGGTCCCCGACGCTGCCGCCGCCGCGCCCGGGCGCACCCGCCCGCTCGC
TGTCCCGCGCACCCCGTAGCGCCTCGGGCTCCCGGGCCGGACAGAGGAGCCAGCCCGGTGCGCC
CCTCCACCTCCTGCTCGGGGGGCTTTAATGAGACACCCACCGCTGCTGTGGGGCCGGCGGGGAG
CAGCACCGCGACGGGGACCGGGGCTGGGCGCTGGAGCCAGAATCGGAACCACGATGTGACTCCG
CCGCCGGGGACCCGTGAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGG
TTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGG
TGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCA
GGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATG
AGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGT
GATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAAT
TACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGG
AGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGA
CATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAA
TACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACA
AAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAG
CAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATT
AAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTAT
TTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATG
TATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAG
AAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGG
TTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGC
TTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACACA
CAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTT
AGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGT
GCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTG
TGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAA
TTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATA
TCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCC
ACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTT
TTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTC
TTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAA
CAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTT
AGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTT
GGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAA
AGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGAC
ATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGA
GGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCA
AAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGG
ACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCAC
ACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCT
GGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGAT
GTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGA
GAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGG
GGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACC
AAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCC
AGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCT
CTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGA
TCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGAT
CACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGG
TGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAAT
TTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGA
AAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAAT
TATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTT
TGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATC
TGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATA
AGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTC
TCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTT
GTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAA
ATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACA
AAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATT
AAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACAT
ATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143814 ⟹ NP_001137286

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,700,455 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,720,774 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,840,883 (-)	NCBI

Sequence:

show sequence

GCAGCCTGGAGCTCCGGGTCCCCGACGCTGCCGCCGCCGCGCCCGGGCGCACCCGCCCGCTCGC
TGTCCCGCGCACCCCGTAGCGCCTCGGGCTCCCGGGCCGGACAGAGGAGCCAGCCCGGTGCGCC
CCTCCACCTCCTGCTCGGGGGGCTTTAATGAGACACCCACCGCTGCTGTGGGGCCGGCGGGGAG
CAGCACCGCGACGGGGACCGGGGCTGGGCGCTGGAGCCAGAATCGGAACCACGATGTGACTCCG
CCGCCGGGGACCCGTGAGGTTTGTGTGGACCCCGAGCATGAGCAGAGATCATTAAAAATTAAAC
TTACAAAGCTGCTAAAGTGGGAAGAAGGAGAACTTGAAGCCACAATTTTTGCACTTGCTTAGAA
GCCATCTAATCTCAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTA
TTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGG
CTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGT
TCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGG
ACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGAT
GCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTAC
CTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGC
TGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACAT
GTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATAC
TTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAA
GGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAA
AAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAA
AGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTG
TATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTAT
AAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAG
GGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTT
GTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTT
AATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACACACAA
CAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGT
ACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCT
GTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGT
TTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTC
CTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCG
ATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACA
TCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTG
ACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTT
GTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAA
GTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGA
ACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGG
TAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGG
TAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATG
AGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGA
ATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAA
CGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACC
TCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACT
CAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGA
GCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTT
TGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAA
CTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGA
CCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAG
ACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGT
GAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTG
CCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCC
CCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCAC
CACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGA
GGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTC
AATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAG
AAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTAT
TTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTTTGA
GGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGT
TAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGA
TACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCT
CTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTG
GCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATG
TAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAA
AACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAA
ACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATA
ATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001143816 ⟹ NP_001137288

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,659,658 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,679,939 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,800,065 (-)	NCBI

Sequence:

show sequence

GCGCGCGCGCACACACACACACACACACAGAGAGAACATCTCTAGTAAAAAGAAAAGTTGAGCT
TTCTTAGCTAGATGTGTGTATTAGCCAGAAAAAGCCAAGGAGTGAAGGGTTTTAGAGAACTGGA
GGAGATAAAGTGGAGTCTGCATATGGGAGGCATTTGAAATGGACTTAAATGTCTTTTTAATGCT
GACTTTTTCAGTTTTCTCCTTACCAGACACATTGTTTTCATGACATTAGCCCCAGGCATAGACA
CATCATTAAAATGAACATGTCAAAAAATGATTTCTGTTTAGAAATAAGCAAAACATTTTCAGTT
GTGACCACCCAGGTGTAGAATAAAGAACAGTGGAATTGGGAGCCCTGAGTTCTAACATAAACTT
TCTTCATGACATAAGGCAAGTCTTCTATGGCCTTTGGTTTCCTTACCTGTAAAACAGGATGGCT
CAATGAAATTATCTTTCTTCTTTGCTATAATAGAGTATCTCTGTGGGAAGAGGAAAAAAAAAGT
CAATTTAAAGGCTCCTTATAGTTCCCCAACTGCTGTTTTATTGTGCTATTCATGCCTAGACATC
ACATAGCTAGAAAGGCCCATCAGACCCCTCAGGCCACTGCTGTTCCTGTCACACATTCCTGCAA
AGGACCATGTTGCTAACTTGAAAAAAATTACTATTAATTACACTTGCAGTTGTTGCTTAGTAAC
ATTTATGATTTTGTGTTTCTCGTGACAGCATGAGCAGAGATCATTAAAAATTAAACTTACAAAG
CTGCTAAAGTGGGAAGAAGGAGAACTTGAAGCCACAATTTTTGCACTTGCTTAGAAGCCATCTA
ATCTCAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATAC
TTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCT
ACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGG
CTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAA
GTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTA
GTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGC
TGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTG
TGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCG
GGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGA
GACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGG
AACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAA
TTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAG
ATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTGTATATATA
CATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAG
TTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAG
TCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGT
TGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGA
ATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACACACAACAAAAATT
TGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATC
TGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCAT
TGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTT
CGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATA
TATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATG
ACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGA
TGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGG
ACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTT
TTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACAC
ATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAA
CAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCAT
GGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCC
TGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAA
CAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGA
GTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCC
TCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTT
TAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGA
CTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTG
GGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCT
GAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGT
AAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGG
AAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAG
GTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCA
CAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTG
GGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAA
AACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGA
CCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAG
CAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTT
CAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGA
CTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATA
TGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAA
TTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGT
TTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCAC
AGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTG
TTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGT
GTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAA
TGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATAT
TTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACC
GCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGT
TTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_001709 ⟹ NP_001700

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,700,455 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,678,552 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,720,774 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,840,883 (-)	NCBI

Sequence:

show sequence

GCAGCCTGGAGCTCCGGGTCCCCGACGCTGCCGCCGCCGCGCCCGGGCGCACCCGCCCGCTCGC
TGTCCCGCGCACCCCGTAGCGCCTCGGGCTCCCGGGCCGGACAGAGGAGCCAGCCCGGTGCGCC
CCTCCACCTCCTGCTCGGGGGGCTTTAATGAGACACCCACCGCTGCTGTGGGGCCGGCGGGGAG
CAGCACCGCGACGGGGACCGGGGCTGGGCGCTGGAGCCAGAATCGGAACCACGATGTGACTCCG
CCGCCGGGGACCCGTGAGGTTTGTGTGGACCCCGAGTTCCACCAGGTGAGAAGAGTGATGACCA
TCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGC
AAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGC
GTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGA
TAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGA
CTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTG
CTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTG
ACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGA
CAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCA
AAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAG
GCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCG
GGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGT
GTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATT
GAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAAT
AATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATT
GGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACAT
TCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAA
TAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAA
AAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTA
AGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAA
TTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGT
ATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGA
GTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTT
GTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACA
AAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTT
GGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCC
TCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATA
TTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGA
GAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTT
TATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAA
CAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGA
ATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCA
TTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCAT
GGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGAC
ATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGT
TCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGC
ATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGA
TGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAA
CCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACT
CAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGT
CTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCT
GACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAG
AGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGT
GGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACA
CCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAAT
TGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAG
ATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACC
ATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGA
AAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAA
CTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAG
GATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAG
TGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGAT
TTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAG
TCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTA
TGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATAT
TATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTA
TTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTT
AAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATAT
TTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_170731 ⟹ NP_733927

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,722,030 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,699,872 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,742,527 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,862,460 (-)	NCBI

Sequence:

show sequence

GATAAGCAACAAGTTCCCCAGCGGTCTTCCCGCCCTAGCCTGACAAGGCGAAGGTTTTCTTACC
TGGCGACAGGGAAATCTCCCGAGCCGAATTCAGCTTCGCCGGAGCCCCAGGTGTGACCTGCGTA
GTGGGCAAGGGAGCGGTGTGCAGGCTGAGTTTTTTTTTTTACAGGGGTACCCTGAAACTCCTCA
CTTTCTCTGGGAACTTTCAGTGCCAGGACCCAGTAACGGGCGGTTAGAAGGCAGCCCTAGGAAA
CACCTGCTACATAGCAGGGCAGTTGGGCAATCATTGGTAACCTCGCTCATTCATTAGAATCACG
TAAGAACTCAAAAGGAAACGTGTCTCTCGGAGTGAGGGCGTTTGCGTAAATCTATAGGTTTTTC
GACATCGATGCCAGTTGCTTTGTCTTCTGTAGTCGCCAAGGTGGTTGAGAGTTTAAGCTTGCGG
ATATTGCAAAGGGTTATTAGATTCATAAGTCACACCAAGTGGTGGGCGATCCACTGAGCAAAGC
CGAACTTCTCACATGATGACTTCAAACAAGACACATTACCTTCCAGCATCTGTTGGGGAGACGA
GATTTTAAGACACTTGAGTCTCCAGGACAGCAAAGGCACAATGTTCCACCAGGTGAGAAGAGTG
ATGACCATCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGA
AAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCT
GGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAA
CACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGG
ACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCT
CTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGC
CACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGG
CGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCC
TGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACA
AAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGT
ACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACAC
TTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGA
TTATATTGAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGA
AAAAAATAATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCT
ATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGC
ATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTA
AAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAA
AACAGAAAAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTA
GACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGC
GTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGAT
GGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCC
ACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTT
GTATGTTGTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAA
CTGAACAAAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTT
GGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTT
CCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTC
TGAAATATTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAA
GCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGAT
TATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGA
GGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAG
AACAGGAATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGG
CATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGT
GGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTG
GAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTC
AAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATA
ATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATG
AGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTT
GAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACC
CCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGG
AAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGA
CAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTT
CATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTG
AAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCA
TTTCACACCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCC
AAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGG
AATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCA
CAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGT
TGTTTGAAAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGT
ATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAA
CTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTG
TGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGAC
CTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTT
TTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGC
TTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTA
AAGATATTATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAAT
TATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGT
TCTATTTAAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTA
AATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_170732 ⟹ NP_733928

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,720,779 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,698,846 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,741,249 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,861,210 (-)	NCBI

Sequence:

show sequence

AATATCAAGTATCACTTAATTAGAGATTTTTAAGCCTTTTCCTCCTGCTGTGCCGGGTGTGTAA
TCCGGGCGATAGGAGTCCATTCAGCACCTTGGACAGAGCCAACGGATTTGTCCGAGGTGGCGGT
ACCCCCAGGTAGTCTTCTTGGCCCCGCTGTAAAGCCAACCCTGTGTCGCCCTTAAAAAGCGTCT
TTTCTGAGGTTCGGCTCACACTGAGATCGGGGCTGGAGAGAGAGTCAGATTTTGGAGCGGAGCG
TTTGGAAAGCGAGCCCCAGTTTGGTCCCCTCATTGAGCTCGCTGAAGTTGGCTTCCTAGCGGTG
TAGGCTGGAATAGACTCTTGGCAAGCTCCGGGTTGGTATACTGGGTTAACTTTGGGAAATGCAA
GTGTTTATCTCCAGGATCTAGCCACCGGGGTGGTGTAAGCCGCAAAGAAGTTCCACCAGGTGAG
AAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCC
CCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATG
GGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACAC
TTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAAC
AATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTC
CTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGT
CCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGG
GTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAA
AGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGG
TTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACC
CAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGA
TAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATA
GATTAGATTATATTGAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCA
GTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCT
ACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAA
AGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAA
AAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCT
TTCAGAAAACAGAAAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTAC
ATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCT
GATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATG
GGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTA
GTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGAT
ACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTA
AGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCA
TTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACA
TTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGC
GCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTC
GTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAAT
GAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCA
TGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTA
GATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGG
AGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGT
GGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTG
GCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACT
GTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTC
TGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTG
ATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACT
AGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAA
GAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGAC
TTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGG
CCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTG
TCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGG
AGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTC
AGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAA
AGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAA
CCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGT
CTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTT
TTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATC
TGCTATATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCAT
CACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCA
ATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTAT
GTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTT
TTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCC
TGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCT
ATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTA
TATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAACCTATTGTAAATA
CAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGT
TTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_170733 ⟹ NP_733929

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,701,621 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,679,729 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,722,093 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,842,046 (-)	NCBI

Sequence:

show sequence

ATTCACCGCGGAGAGGGCTGCTCTCGCTGCCGCTCCCCCCGGCGAACTAGCATGAAATCTCCCT
GCCTCTGCCGAGATCAAATGGAGCTTCTCGCTGATGGGGTGCGAGTATTACCTCCGCCATGCAA
TTTCCACTATCAATAATTTAACTTCTTTGCTGCAGAACAGAAGGAGTACATACCGGGCACCAAA
GACTCGCGCCCCCTCCCCCCTTTAATTAAGCGAAGGGAACGTGAAAAAATAATAGAGTGTGGGA
GTTTTGGGGCCGAAGTCTTTCCCGGAGCAGCTGCCTTGATGGTTACTTTGACAAGTAGTGACTG
AAAAGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATACTT
TGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTAC
CCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCT
TGACATCATTGGCTGACACTTTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGT
TCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGT
CAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTG
CAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTG
TGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGG
ACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGA
CCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAA
CTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATT
GGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGAT
AGTGGATTTATGTTGTATAGATTAGATTATATTGAGACAAAAATTATCTATTTGTATATATACA
TAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAGTT
TATACAGTACAGTGGTTCTACAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTC
ATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTG
CCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAAT
TGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAACACACACACACACAACAAAAATTTG
AACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTG
TTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTG
CTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCG
TTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATA
TATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATGAC
TAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGATG
CACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGAC
CTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTT
AAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACACAT
TGTGTCACATCATGACACTCGTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACA
ACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGG
CTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTG
TATCAACCCAGAAACACCTAGATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAACA
GCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGT
GGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTC
TGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTA
AGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACT
TATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGG
AGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGA
ACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAA
GGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAA
ATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGT
GCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACA
GCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGG
TTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAA
CTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGACC
AGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCA
AAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCA
GTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACT
TTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATATG
TAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATT
TAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTT
CATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAG
TCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTT
CGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGT
TTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATG
TCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATATTT
ATTGTATTTTAGTATATTTATATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGC
ATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGTTT
TAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_170734 ⟹ NP_733930

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,699,667 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,677,756 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,719,953 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,840,095 (-)	NCBI

Sequence:

show sequence

ACACGGCTACCTGCTCCCCAGGAATTGAGACTGAAGTGGACTTACAAGTCCGAAGCCAATGTAG
CTTGGAAAACTTGGGAGGCGGAATTCCTACCGCTGGGAACTGAAAGGGTCTGCGACACTCTCGG
GCAGGCCGAACCCACATCTCTACCCATCCTGCGCCCCTCTTCTGAAGCGCCCTCCAGGGAAGTT
AAGAGTTTTGACTTTCGGGGAGTGGTTGGGATGTACGTGGGGGATTCTTGACTCGGGTTAGTCT
CTGGGGATGCAGAGCCGGGAAGAGGAATGGTTCCACCAGGTGAGAAGAGTGATGACCATCCTTT
TCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCCCCATGAAAGAAGCAAACAT
CCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGGGACTCTGGAGAGCGTGAAT
GGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACTTTCGAACACGTGATAGAAG
AGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACAATAAGGACGCAGACTTGTA
CACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCCTCTTCTCTTTCTGCTGGAG
GAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTCCGGCGCCACTCTGACCCTG
CCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGGTAACGGCGGCAGACAAAAA
GACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAAGGTCCCTGTATCAAAAGGC
CAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGTTACACAAAAGAAGGCTGCA
GGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCCAGTCGTACGTGCGGGCCCT
TACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGATAGACACTTCTTGTGTATGT
ACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAGATTAGATTATATTGAGACA
AAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAGTTAAGAAAAAAATAATTTT
ATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTACAATCTATTTATTGGACAT
GTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAAGTCTGCATTACATTCCTTG
ATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAAAAGTTAAAAAAAATAATAA
ATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTTTCAGAAAACAGAAAAAAAA
CACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTACATTTTAGACAGTAAGTATC
TTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCTGATAGCGTTGGAATTAAAA
CAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATGGGGGATGGGGGGTATATTT
TTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTAGTTCCCACAGGGAGTAGAG
ATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGATACATTTGTATGTTGTGAAG
ATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTAAGGCAACTGAACAAAAAAA
TGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCATTCTTTGGGCGTTGGTCAG
AGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACATTCTTTCCCCCCCTCCCCC
TCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGCGCGTTCTGAAATATTTTAC
CACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTCGTATAAGCATGGAGAACAG
TGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAATGAAGATTATTTTTTATGAG
GAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCATGGTGAGGCTTAACAATGT
CTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTAGATCAGAACAGGAATCCAC
ATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGGAGTTGGCATTGCATTTACC
GGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGTGGAGGTGGGGCATGGTATT
TGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTGGCTCTGGAATGACATGTGT
CAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACTGTGCTCAAGAGGTTCTCGA
CTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTCTGGATAATTTTGCATAAAA
TTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTGATCATGAGATTGATGCAAT
GAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACTAGACTTGAGGAAACCAGGG
TTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAAGAAACCCCAAACTCAGGCC
GAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGACTTCGGGAAGGTGTCTGGAC
ATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGGCCAGGACAGAGCTGACAAA
ATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTGTCTGTTCATGGAGAGGGTC
CCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGGAGCCTGAAATAGTGGTTCT
TGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTCAGCCCATTTCACACCTGAA
AATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAAAGCCCCAAGCAATTGCTGC
ATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAACCCAGGAATGAAGATACCA
TCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGTCTTTCACAGTACCATCTGA
ATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTTTTGTGTTGTTTGAAAATAT
TATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATCTGCTGTATGTCAACTTTAT
GCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCATCACAAACTTAAAGGATTGC
AAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCAATTGTGTGGTCAGTGGCTC
TTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTATGTTGACCTAAGATTTATTT
TGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTTTTGTTTTTTAAAGTCTTGC
TGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCCTGTTGCTTTTTTATGGCGA
TTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCTATGGTAAAGATATTATTCA
CCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTATATAATTATGTTATTGAAA
AAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAATACAAGTTCTATTTAAGTGT
ACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATGTTTTTAAATATATTTTCAA
AGTACATAAAA

hide sequence

RefSeq Acc Id:

NM_170735 ⟹ NP_733931

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,654,893 - 27,659,658 (-)	NCBI
GRCh37	11	27,676,440 - 27,743,605 (-)	ENTREZGENE
Build 36	11	27,633,016 - 27,637,249 (-)	NCBI Archive
HuRef	11	27,374,586 - 27,441,772 (-)	ENTREZGENE
CHM1_1	11	27,675,184 - 27,679,939 (-)	NCBI
T2T-CHM13v2.0	11	27,795,301 - 27,800,065 (-)	NCBI

Sequence:

show sequence

GCGCGCGCGCACACACACACACACACACAGAGAGAACATCTCTAGTAAAAAGAAAAGTTGAGCT
TTCTTAGCTAGATGTGTGTATTAGCCAGAAAAAGCCAAGGAGTGAAGGGTTTTAGAGAACTGGA
GGAGATAAAGTGGAGTCTGCATATGGGAGGCATTTGAAATGGACTTAAATGTCTTTTTAATGCT
GACTTTTTCAGTTTTCTCCTTACCAGACACATTGTTTTCATGACATTAGCCCCAGGCATAGACA
CATCATTAAAATGAACATGTCAAAAAATGATTTCTGTTTAGAAATAAGCAAAACATTTTCAGTT
GTGACCACCCAGGTGTAGAATAAAGAACAGTGGAATTGGGAGCCCTGAGTTCTAACATAAACTT
TCTTCATGACATAAGGCAAGTCTTCTATGGCCTTTGGTTTCCTTACCTGTAAAACAGGATGGCT
CAATGAAATTATCTTTCTTCTTTGCTATAATAGAGTATCTCTGTGGGAAGAGGAAAAAAAAAGT
CAATTTAAAGGCTCCTTATAGTTCCCCAACTGCTGTTTTATTGTGCTATTCATGCCTAGACATC
ACATAGCTAGAAAGGCCCATCAGACCCCTCAGGCCACTGCTGTTCCTGTCACACATTCCTGCAA
AGGACCATGTTGCTAACTTGAAAAAAATTACTATTAATTACACTTGCAGTTGTTGCTTAGTAAC
ATTTATGATTTTGTGTTTCTCGTGACAGCATGAGCAGAGATCATTAAAAATTAAACTTACAAAG
CTGCTAAAGTGGGAAGAAGGAGAACTTGAAGCCACAATTTTTGCACTTGCTTAGAAGCCATCTA
ATCTCAGGTTTATATGCTAGATCTTGGGGGAAACACTGCATGTCTCTGGTTTATATTAAACCAC
ATACAGCACACTACTGACACTGATTTGTGTCTGGTGCAGCTGGAGTTTATCACCAAGACATAAA
AAAACCTTGACCCTGCAGAATGGCCTGGAATTACAATCAGATGGGCCACATGGCATCCCGGTGA
AAGAAAGCCCTAACCAGTTTTCTGTCTTGTTTCTGCTTTCTCCCTACAGTTCCACCAGGTGAGA
AGAGTGATGACCATCCTTTTCCTTACTATGGTTATTTCATACTTTGGTTGCATGAAGGCTGCCC
CCATGAAAGAAGCAAACATCCGAGGACAAGGTGGCTTGGCCTACCCAGGTGTGCGGACCCATGG
GACTCTGGAGAGCGTGAATGGGCCCAAGGCAGGTTCAAGAGGCTTGACATCATTGGCTGACACT
TTCGAACACGTGATAGAAGAGCTGTTGGATGAGGACCAGAAAGTTCGGCCCAATGAAGAAAACA
ATAAGGACGCAGACTTGTACACGTCCAGGGTGATGCTCAGTAGTCAAGTGCCTTTGGAGCCTCC
TCTTCTCTTTCTGCTGGAGGAATACAAAAATTACCTAGATGCTGCAAACATGTCCATGAGGGTC
CGGCGCCACTCTGACCCTGCCCGCCGAGGGGAGCTGAGCGTGTGTGACAGTATTAGTGAGTGGG
TAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACAGTCCTTGAAAA
GGTCCCTGTATCAAAAGGCCAACTGAAGCAATACTTCTACGAGACCAAGTGCAATCCCATGGGT
TACACAAAAGAAGGCTGCAGGGGCATAGACAAAAGGCATTGGAACTCCCAGTGCCGAACTACCC
AGTCGTACGTGCGGGCCCTTACCATGGATAGCAAAAAGAGAATTGGCTGGCGATTCATAAGGAT
AGACACTTCTTGTGTATGTACATTGACCATTAAAAGGGGAAGATAGTGGATTTATGTTGTATAG
ATTAGATTATATTGAGACAAAAATTATCTATTTGTATATATACATAACAGGGTAAATTATTCAG
TTAAGAAAAAAATAATTTTATGAACTGCATGTATAAATGAAGTTTATACAGTACAGTGGTTCTA
CAATCTATTTATTGGACATGTCCATGACCAGAAGGGAAACAGTCATTTGCGCACAACTTAAAAA
GTCTGCATTACATTCCTTGATAATGTTGTGGTTTGTTGCCGTTGCCAAGAACTGAAAACATAAA
AAGTTAAAAAAAATAATAAATTGCATGCTGCTTTAATTGTGAATTGATAATAAACTGTCCTCTT
TCAGAAAACAGAAAAAAAACACACACACACACAACAAAAATTTGAACCAAAACATTCCGTTTAC
ATTTTAGACAGTAAGTATCTTCGTTCTTGTTAGTACTATATCTGTTTTACTGCTTTTAACTTCT
GATAGCGTTGGAATTAAAACAATGTCAAGGTGCTGTTGTCATTGCTTTACTGGCTTAGGGGATG
GGGGATGGGGGGTATATTTTTGTTTGTTTTGTGTTTTTTTTTCGTTTGTTTGTTTTGTTTTTTA
GTTCCCACAGGGAGTAGAGATGGGGAAAGAATTCCTACAATATATATTCTGGCTGATAAAAGAT
ACATTTGTATGTTGTGAAGATGTTTGCAATATCGATCAGATGACTAGAAAGTGAATAAAAATTA
AGGCAACTGAACAAAAAAATGCTCACACTCCACATCCCGTGATGCACCTCCCAGGCCCCGCTCA
TTCTTTGGGCGTTGGTCAGAGTAAGCTGCTTTTGACGGAAGGACCTATGTTTGCTCAGAACACA
TTCTTTCCCCCCCTCCCCCTCTGGTCTCCTCTTTGTTTTGTTTTAAGGAAGAAAAATCAGTTGC
GCGTTCTGAAATATTTTACCACTGCTGTGAACAAGTGAACACATTGTGTCACATCATGACACTC
GTATAAGCATGGAGAACAGTGATTTTTTTTTAGAACAGAAAACAACAAAAAATAACCCCAAAAT
GAAGATTATTTTTTATGAGGAGTGAACATTTGGGTAAATCATGGCTAAGCTTAAAAAAAACTCA
TGGTGAGGCTTAACAATGTCTTGTAAGCAAAAGGTAGAGCCCTGTATCAACCCAGAAACACCTA
GATCAGAACAGGAATCCACATTGCCAGTGACATGAGACTGAACAGCCAAATGGAGGCTATGTGG
AGTTGGCATTGCATTTACCGGCAGTGCGGGAGGAATTTCTGAGTGGCCATCCCAAGGTCTAGGT
GGAGGTGGGGCATGGTATTTGAGACATTCCAAAACGAAGGCCTCTGAAGGACCCTTCAGAGGTG
GCTCTGGAATGACATGTGTCAAGCTGCTTGGACCTCGTGCTTTAAGTGCCTACATTATCTAACT
GTGCTCAAGAGGTTCTCGACTGGAGGACCACACTCAAGCCGACTTATGCCCACCATCCCACCTC
TGGATAATTTTGCATAAAATTGGATTAGCCTGGAGCAGGTTGGGAGCCAAATGTGGCATTTGTG
ATCATGAGATTGATGCAATGAGATAGAAGATGTTTGCTACCTGAACACTTATTGCTTTGAAACT
AGACTTGAGGAAACCAGGGTTTATCTTTTGAGAACTTTTGGTAAGGGAAAAGGGAACAGGAAAA
GAAACCCCAAACTCAGGCCGAATGATCAAGGGGACCCATAGGAAATCTTGTCCAGAGACAAGAC
TTCGGGAAGGTGTCTGGACATTCAGAACACCAAGACTTGAAGGTGCCTTGCTCAATGGAAGAGG
CCAGGACAGAGCTGACAAAATTTTGCTCCCCAGTGAAGGCCACAGCAACCTTCTGCCCATCCTG
TCTGTTCATGGAGAGGGTCCCTGCCTCACCTCTGCCATTTTGGGTTAGGAGAAGTCAAGTTGGG
AGCCTGAAATAGTGGTTCTTGGAAAAATGGATCCCCAGTGAAAACTAGAGCTCTAAGCCCATTC
AGCCCATTTCACACCTGAAAATGTTAGTGATCACCACTTGGACCAGCATCCTTAAGTATCAGAA
AGCCCCAAGCAATTGCTGCATCTTAGTAGGGTGAGGGATAAGCAAAAGAGGATGTTCACCATAA
CCCAGGAATGAAGATACCATCAGCAAAGAATTTCAATTTGTTCAGTCTTTCATTTAGAGCTAGT
CTTTCACAGTACCATCTGAATACCTCTTTGAAAGAAGGAAGACTTTACGTAGTGTAGATTTGTT
TTGTGTTGTTTGAAAATATTATCTTTGTAATTATTTTTAATATGTAAGGAATGCTTGGAATATC
TGCTGTATGTCAACTTTATGCAGCTTCCTTTTGAGGGACAAATTTAAAACAAACAACCCCCCAT
CACAAACTTAAAGGATTGCAAGGGCCAGATCTGTTAAGTGGTTTCATAGGAGACACATCCAGCA
ATTGTGTGGTCAGTGGCTCTTTTACCCAATAAGATACATCACAGTCACATGCTTGATGGTTTAT
GTTGACCTAAGATTTATTTTGTTAAAATCTCTCTCTGTTGTGTTCGTTCTTGTTCTGTTTTGTT
TTGTTTTTTAAAGTCTTGCTGTGGTCTCTTTGTGGCAGAAGTGTTTCATGCATGGCAGCAGGCC
TGTTGCTTTTTTATGGCGATTCCCATTGAAAATGTAAGTAAATGTCTGTGGCCTTGTTCTCTCT
ATGGTAAAGATATTATTCACCATGTAAAACAAAAAACAATATTTATTGTATTTTAGTATATTTA
TATAATTATGTTATTGAAAAAAATTGGCATTAAAACTTAACCGCATCAGAAGCCTATTGTAAAT
ACAAGTTCTATTTAAGTGTACTAATTAACATATAATATATGTTTTAAATATAGAATTTTTAATG
TTTTTAAATATATTTTCAAAGTACATAAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001137277	(Get FASTA)	NCBI Sequence Viewer
	NP_001137278	(Get FASTA)	NCBI Sequence Viewer
	NP_001137279	(Get FASTA)	NCBI Sequence Viewer
	NP_001137280	(Get FASTA)	NCBI Sequence Viewer
	NP_001137281	(Get FASTA)	NCBI Sequence Viewer
	NP_001137282	(Get FASTA)	NCBI Sequence Viewer
	NP_001137283	(Get FASTA)	NCBI Sequence Viewer
	NP_001137284	(Get FASTA)	NCBI Sequence Viewer
	NP_001137285	(Get FASTA)	NCBI Sequence Viewer
	NP_001137286	(Get FASTA)	NCBI Sequence Viewer
	NP_001137288	(Get FASTA)	NCBI Sequence Viewer
	NP_001700	(Get FASTA)	NCBI Sequence Viewer
	NP_733927	(Get FASTA)	NCBI Sequence Viewer
	NP_733928	(Get FASTA)	NCBI Sequence Viewer
	NP_733929	(Get FASTA)	NCBI Sequence Viewer
	NP_733930	(Get FASTA)	NCBI Sequence Viewer
	NP_733931	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA51820	(Get FASTA)	NCBI Sequence Viewer
	AAA69805	(Get FASTA)	NCBI Sequence Viewer
	AAA96140	(Get FASTA)	NCBI Sequence Viewer
	AAG47514	(Get FASTA)	NCBI Sequence Viewer
	AAH29795	(Get FASTA)	NCBI Sequence Viewer
	AAK92487	(Get FASTA)	NCBI Sequence Viewer
	AAL23557	(Get FASTA)	NCBI Sequence Viewer
	AAL23558	(Get FASTA)	NCBI Sequence Viewer
	AAL23559	(Get FASTA)	NCBI Sequence Viewer
	AAL23560	(Get FASTA)	NCBI Sequence Viewer
	AAL23561	(Get FASTA)	NCBI Sequence Viewer
	AAL23562	(Get FASTA)	NCBI Sequence Viewer
	AAL23563	(Get FASTA)	NCBI Sequence Viewer
	AAL23564	(Get FASTA)	NCBI Sequence Viewer
	AAL23565	(Get FASTA)	NCBI Sequence Viewer
	AAL23571	(Get FASTA)	NCBI Sequence Viewer
	AAO15434	(Get FASTA)	NCBI Sequence Viewer
	AAR14686	(Get FASTA)	NCBI Sequence Viewer
	AAT74399	(Get FASTA)	NCBI Sequence Viewer
	ABB51155	(Get FASTA)	NCBI Sequence Viewer
	ABS29021	(Get FASTA)	NCBI Sequence Viewer
	ABS29022	(Get FASTA)	NCBI Sequence Viewer
	ABS29023	(Get FASTA)	NCBI Sequence Viewer
	ABS29024	(Get FASTA)	NCBI Sequence Viewer
	ABS29025	(Get FASTA)	NCBI Sequence Viewer
	ABS32249	(Get FASTA)	NCBI Sequence Viewer
	ABS32250	(Get FASTA)	NCBI Sequence Viewer
	ABS32251	(Get FASTA)	NCBI Sequence Viewer
	ABS32252	(Get FASTA)	NCBI Sequence Viewer
	ABS32253	(Get FASTA)	NCBI Sequence Viewer
	ABS32254	(Get FASTA)	NCBI Sequence Viewer
	ABS32255	(Get FASTA)	NCBI Sequence Viewer
	ABS32256	(Get FASTA)	NCBI Sequence Viewer
	ABS32257	(Get FASTA)	NCBI Sequence Viewer
	ABS32258	(Get FASTA)	NCBI Sequence Viewer
	ABS32259	(Get FASTA)	NCBI Sequence Viewer
	ABS32260	(Get FASTA)	NCBI Sequence Viewer
	ABS32261	(Get FASTA)	NCBI Sequence Viewer
	AGR50950	(Get FASTA)	NCBI Sequence Viewer
	AKB90516	(Get FASTA)	NCBI Sequence Viewer
	ALQ33401	(Get FASTA)	NCBI Sequence Viewer
	ALQ33402	(Get FASTA)	NCBI Sequence Viewer
	ALQ33403	(Get FASTA)	NCBI Sequence Viewer
	BAB55545	(Get FASTA)	NCBI Sequence Viewer
	BAB55546	(Get FASTA)	NCBI Sequence Viewer
	BAB55547	(Get FASTA)	NCBI Sequence Viewer
	BAB55548	(Get FASTA)	NCBI Sequence Viewer
	BAB55549	(Get FASTA)	NCBI Sequence Viewer
	BAF82452	(Get FASTA)	NCBI Sequence Viewer
	BAF82542	(Get FASTA)	NCBI Sequence Viewer
	CAA42761	(Get FASTA)	NCBI Sequence Viewer
	CAA62632	(Get FASTA)	NCBI Sequence Viewer
	EAW68274	(Get FASTA)	NCBI Sequence Viewer
	EAW68275	(Get FASTA)	NCBI Sequence Viewer
	EAW68276	(Get FASTA)	NCBI Sequence Viewer
	EAW68277	(Get FASTA)	NCBI Sequence Viewer
	EAW68278	(Get FASTA)	NCBI Sequence Viewer
	EAW68279	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000320002
	ENSP00000320002.6
	ENSP00000349084
	ENSP00000349084.4
	ENSP00000379302
	ENSP00000379302.3
	ENSP00000379305
	ENSP00000379305.3
	ENSP00000379307
	ENSP00000379307.3
	ENSP00000379309
	ENSP00000379309.2
	ENSP00000389345
	ENSP00000389345.2
	ENSP00000400502
	ENSP00000400502.1
	ENSP00000414303
	ENSP00000414303.1
	ENSP00000432035
	ENSP00000432035.1
	ENSP00000432376
	ENSP00000432376.1
	ENSP00000432727.1
	ENSP00000435564
	ENSP00000435564.1
	ENSP00000435805
	ENSP00000435805.1
	ENSP00000437138
	ENSP00000437138.1
GenBank Protein	P23560	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_733927 ⟸ NM_170731
- Peptide Label:	isoform b precursor
- UniProtKB:	A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFHQVRRVMTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGL TSLADTFEHVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAA NMSMRVRRHSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYET KCNPMGYTKEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137277 ⟸ NM_001143805
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137278 ⟸ NM_001143806
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_733928 ⟸ NM_170732
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137279 ⟸ NM_001143807
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_733929 ⟸ NM_170733
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137280 ⟸ NM_001143808
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137281 ⟸ NM_001143809
- Peptide Label:	isoform d precursor
- UniProtKB:	P23560 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLCAISLCARVRKLRSAGRCGKFHQVRRVMTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYP GVRTHGTLESVNGPKAGSRGLTSLADTFEHVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQ VPLEPPLLFLLEEYKNYLDAANMSMRVRRHSDPARRGELSVCDSISEWVTAADKKTAVDMSGGT VTVLEKVPVSKGQLKQYFYETKCNPMGYTKEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIG WRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137282 ⟸ NM_001143810
- Peptide Label:	isoform e
- UniProtKB:	P23560 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MCGATSFLHECTRLILVTTQNAEFLQKGLQVHTCFGVYPHASVWHDCASQKKGCAVYLHVSVEF NKLIPENGFIKFHQVRRVMTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESV NGPKAGSRGLTSLADTFEHVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLL EEYKNYLDAANMSMRVRRHSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSK GQLKQYFYETKCNPMGYTKEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCV CTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137283 ⟸ NM_001143811
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137284 ⟸ NM_001143812
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137285 ⟸ NM_001143813
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001700 ⟸ NM_001709
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_001137286 ⟸ NM_001143814
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_733930 ⟸ NM_170734
- Peptide Label:	isoform c precursor
- UniProtKB:	P23560 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MQSREEEWFHQVRRVMTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGP KAGSRGLTSLADTFEHVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEY KNYLDAANMSMRVRRHSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQL KQYFYETKCNPMGYTKEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTL TIKRGR hide sequence

RefSeq Acc Id:	NP_001137288 ⟸ NM_001143816
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

RefSeq Acc Id:	NP_733931 ⟸ NM_170735
- Peptide Label:	isoform a preproprotein
- UniProtKB:	Q9BYY7 (UniProtKB/Swiss-Prot), Q6YNR3 (UniProtKB/Swiss-Prot), Q6YNR2 (UniProtKB/Swiss-Prot), Q6DN19 (UniProtKB/Swiss-Prot), Q598Q1 (UniProtKB/Swiss-Prot), D3DQZ2 (UniProtKB/Swiss-Prot), A7LA92 (UniProtKB/Swiss-Prot), A7LA85 (UniProtKB/Swiss-Prot), Q9UC24 (UniProtKB/Swiss-Prot), P23560 (UniProtKB/Swiss-Prot), A0A0E3SU01 (UniProtKB/TrEMBL), A0A0S2Z3E7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFE HVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRR HSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYT KEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR hide sequence

Ensembl Acc Id:

ENSP00000414303 ⟸ ENST00000438929

Ensembl Acc Id:

ENSP00000389345 ⟸ ENST00000439476

Ensembl Acc Id:

ENSP00000433003 ⟸ ENST00000530786

Ensembl Acc Id:

ENSP00000435564 ⟸ ENST00000530861

Ensembl Acc Id:

ENSP00000435805 ⟸ ENST00000532997

Ensembl Acc Id:

ENSP00000432376 ⟸ ENST00000533246

Ensembl Acc Id:

ENSP00000432727 ⟸ ENST00000533131

Ensembl Acc Id:

ENSP00000400502 ⟸ ENST00000418212

Ensembl Acc Id:

ENSP00000320002 ⟸ ENST00000314915

Ensembl Acc Id:

ENSP00000432035 ⟸ ENST00000525950

Ensembl Acc Id:

ENSP00000437138 ⟸ ENST00000525528

Ensembl Acc Id:

ENSP00000349084 ⟸ ENST00000356660

Ensembl Acc Id:

ENSP00000389564 ⟸ ENST00000420794

Ensembl Acc Id:

ENSP00000379302 ⟸ ENST00000395978

Ensembl Acc Id:

ENSP00000379309 ⟸ ENST00000395986

Ensembl Acc Id:

ENSP00000379307 ⟸ ENST00000395983

Ensembl Acc Id:

ENSP00000379304 ⟸ ENST00000395980

Ensembl Acc Id:

ENSP00000379305 ⟸ ENST00000395981

Protein Domains

Nerve growth factor-related

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P23560-F1-model_v2	AlphaFold	P23560	1-247	view protein structure

Promoters

RGD ID:

6788516

Promoter ID:

HG_KWN:12523

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000395983, NM_001143808, NM_001143809, NM_001143810, NM_001143811, NM_001143812, NM_001143813, NM_001143814, NM_001709, NM_170734

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	27,678,349 - 27,678,849 (-)	MPROMDB

RGD ID:

7219899

Promoter ID:

EPDNEW_H15695

Type:

initiation region

Name:

BDNF_1

Description:

brain derived neurotrophic factor

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H15696 EPDNEW_H15697

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,700,455 - 27,700,515	EPDNEW

RGD ID:

7219901

Promoter ID:

EPDNEW_H15696

Type:

initiation region

Name:

BDNF_3

Description:

brain derived neurotrophic factor

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H15695 EPDNEW_H15697

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,701,621 - 27,701,681	EPDNEW

RGD ID:

7219903

Promoter ID:

EPDNEW_H15697

Type:

single initiation site

Name:

BDNF_2

Description:

brain derived neurotrophic factor

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H15695 EPDNEW_H15696

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	27,719,565 - 27,719,625	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:1033	AgrOrtholog
COSMIC	BDNF	COSMIC
Ensembl Genes	ENSG00000176697	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000314915	ENTREZGENE
	ENST00000314915.6	UniProtKB/Swiss-Prot
	ENST00000356660	ENTREZGENE
	ENST00000356660.9	UniProtKB/Swiss-Prot
	ENST00000395978	ENTREZGENE
	ENST00000395978.7	UniProtKB/Swiss-Prot
	ENST00000395981	ENTREZGENE
	ENST00000395981.7	UniProtKB/Swiss-Prot
	ENST00000395983	ENTREZGENE
	ENST00000395983.7	UniProtKB/Swiss-Prot
	ENST00000395986	ENTREZGENE
	ENST00000395986.6	UniProtKB/Swiss-Prot
	ENST00000418212	ENTREZGENE
	ENST00000418212.5	UniProtKB/Swiss-Prot
	ENST00000438929	ENTREZGENE
	ENST00000438929.5	UniProtKB/Swiss-Prot
	ENST00000439476	ENTREZGENE
	ENST00000439476.6	UniProtKB/Swiss-Prot
	ENST00000525528	ENTREZGENE
	ENST00000525528.1	UniProtKB/Swiss-Prot
	ENST00000525950	ENTREZGENE
	ENST00000525950.5	UniProtKB/Swiss-Prot
	ENST00000530861	ENTREZGENE
	ENST00000530861.5	UniProtKB/Swiss-Prot
	ENST00000532997	ENTREZGENE
	ENST00000532997.5	UniProtKB/Swiss-Prot
	ENST00000533131.5	UniProtKB/Swiss-Prot
	ENST00000533246	ENTREZGENE
	ENST00000533246.5	UniProtKB/Swiss-Prot
	ENST00000584049	ENTREZGENE
Gene3D-CATH	2.10.90.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000176697	GTEx
HGNC ID	HGNC:1033	ENTREZGENE
Human Proteome Map	BDNF	Human Proteome Map
InterPro	Brain-der_neurotrophic_factor	UniProtKB/Swiss-Prot
	Cystine-knot_cytokine	UniProtKB/Swiss-Prot
	Nerve_growth_factor-like	UniProtKB/Swiss-Prot
	Nerve_growth_factor-rel	UniProtKB/Swiss-Prot
	Nerve_growth_factor_CS	UniProtKB/Swiss-Prot
KEGG Report	hsa:627	UniProtKB/Swiss-Prot
NCBI Gene	627	ENTREZGENE
OMIM	113505	OMIM
PANTHER	PTHR11589	UniProtKB/Swiss-Prot
	PTHR11589:SF3	UniProtKB/Swiss-Prot
Pfam	NGF	UniProtKB/Swiss-Prot
PharmGKB	BDNF	RGD
	PA31891	PharmGKB
PIRSF	NGF	UniProtKB/Swiss-Prot
PRINTS	BDNFACTOR	UniProtKB/Swiss-Prot
	NGF	UniProtKB/Swiss-Prot
PROSITE	NGF_1	UniProtKB/Swiss-Prot
	NGF_2	UniProtKB/Swiss-Prot
SMART	NGF	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF57501	UniProtKB/Swiss-Prot
UniProt	A0A0E3SU01	ENTREZGENE, UniProtKB/TrEMBL
	A0A0S2Z3E7	ENTREZGENE, UniProtKB/TrEMBL
	A0A0S2Z3M9_HUMAN	UniProtKB/TrEMBL
	A7LA85	ENTREZGENE
	A7LA92	ENTREZGENE
	BDNF_HUMAN	UniProtKB/Swiss-Prot
	D3DQZ2	ENTREZGENE
	E9PMP3_HUMAN	UniProtKB/TrEMBL
	P23560	ENTREZGENE
	Q304R1_HUMAN	UniProtKB/TrEMBL
	Q598Q1	ENTREZGENE
	Q6DN19	ENTREZGENE
	Q6T2C9_HUMAN	UniProtKB/TrEMBL
	Q6YNR1_HUMAN	UniProtKB/TrEMBL
	Q6YNR2	ENTREZGENE
	Q6YNR3	ENTREZGENE
	Q9BYY7	ENTREZGENE
	Q9UC24	ENTREZGENE
UniProt Secondary	A7LA85	UniProtKB/Swiss-Prot
	A7LA92	UniProtKB/Swiss-Prot
	D3DQZ2	UniProtKB/Swiss-Prot
	Q598Q1	UniProtKB/Swiss-Prot
	Q6DN19	UniProtKB/Swiss-Prot
	Q6YNR2	UniProtKB/Swiss-Prot
	Q6YNR3	UniProtKB/Swiss-Prot
	Q9BYY7	UniProtKB/Swiss-Prot
	Q9UC24	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-06-07	BDNF	brain derived neurotrophic factor	BDNF	brain-derived neurotrophic factor	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Disease Annotations - GAD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Manual Human Phenotype Annotations - RGD

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Disease Annotations - GAD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Manual Human Phenotype Annotations - RGD

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar