MLXIPL (MLX interacting protein like) - Rat Genome Database

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Gene: MLXIPL (MLX interacting protein like) Homo sapiens
Analyze
Symbol: MLXIPL
Name: MLX interacting protein like
RGD ID: 1343873
HGNC Page HGNC
Description: Exhibits protein heterodimerization activity and transcription factor binding activity. Is predicted to contribute to DNA binding activity. Involved in several processes, including negative regulation of cell cycle arrest; positive regulation of lipid biosynthetic process; and regulation of phosphorylation. Localizes to cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: bHLHd14; carbohydrate response element binding protein; carbohydrate-responsive element-binding protein; CHREBP; class D basic helix-loop-helix protein 14; MIO; MLX; MLX interacting protein-like; Mlx interactor; MLX-interacting protein-like; MONDOB; WBSCR14; Williams Beuren syndrome chromosome region 14; Williams-Beuren syndrome chromosomal region 14 protein; Williams-Beuren syndrome chromosome region 14 protein 1; Williams-Beuren syndrome chromosome region 14 protein 2; Williams-Beuren syndrome chromosome region 14 protein 3; WS basic-helix-loop-helix leucine zipper protein; WS-bHLH
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl773,593,194 - 73,624,543 (-)EnsemblGRCh38hg38GRCh38
GRCh38773,593,201 - 73,624,522 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37773,007,532 - 73,038,852 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36772,645,460 - 72,676,806 (-)NCBINCBI36hg18NCBI36
Build 34772,452,174 - 72,483,521NCBI
Celera768,485,730 - 68,517,088 (-)NCBI
Cytogenetic Map7q11.23NCBI
HuRef768,888,586 - 68,920,882 (-)NCBIHuRef
CHM1_1773,153,232 - 73,184,535 (-)NCBICHM1_1
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(RS)-coclaurine  (ISO)
(RS)-norcoclaurine  (ISO)
(S)-coclaurine  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-(4-chlorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime  (EXP)
aflatoxin B1  (EXP,ISO)
aldehydo-D-glucose  (ISO)
amiodarone  (ISO)
atorvastatin calcium  (ISO)
atrazine  (ISO)
benzo[a]pyrene  (EXP,ISO)
bexarotene  (EXP)
bisphenol A  (EXP,ISO)
cadmium dichloride  (ISO)
caffeine  (ISO)
carbon nanotube  (ISO)
cetirizine  (ISO)
chlordecone  (ISO)
cholesterol  (ISO)
choline  (ISO)
ciguatoxin CTX1B  (ISO)
cisplatin  (EXP)
copper(II) sulfate  (EXP)
CU-O LINKAGE  (EXP)
cyclosporin A  (EXP)
D-glucose  (ISO)
dexamethasone  (EXP,ISO)
dicrotophos  (EXP)
dioxygen  (ISO)
disodium selenite  (ISO)
dorsomorphin  (EXP)
enilconazole  (EXP)
entinostat  (EXP)
ethanol  (ISO)
farnesol  (EXP)
Fexofenadine hydrochloride  (ISO)
folic acid  (ISO)
fructose  (ISO)
furan  (ISO)
glucose  (ISO)
GW 3965  (EXP)
GW 4064  (EXP)
GW 7647  (EXP)
indometacin  (EXP)
irinotecan  (ISO)
L-methionine  (ISO)
monosodium L-glutamate  (ISO)
N-[2-(4-bromocinnamylamino)ethyl]isoquinoline-5-sulfonamide  (ISO)
nefazodone  (ISO)
nicotinic acid  (ISO)
oleic acid  (EXP)
paracetamol  (EXP,ISO)
Paxilline  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (EXP)
phenformin  (ISO)
pirinixic acid  (ISO)
propamocarb  (ISO)
propiconazole  (EXP)
rotenone  (ISO)
salvianolic acid B  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (ISO)
sodium arsenite  (ISO)
sucrose  (ISO)
sulforaphane  (EXP)
tamoxifen  (ISO)
taurine  (ISO)
tebuconazole  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
tris(2-butoxyethyl) phosphate  (EXP)
trovafloxacin  (ISO)
urethane  (EXP)
valproic acid  (EXP)
yohimbine  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
chromatin  (ISA)
cytoplasm  (ISO,ISS)
cytosol  (IDA,TAS)
nucleoplasm  (IDA,TAS)
nucleus  (IBA,ISO,ISS,NAS)
transcription regulator complex  (NAS)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Abnormality of refraction  (IAGP)
Amblyopia  (IAGP)
Anxiety  (IAGP)
Arnold-Chiari type I malformation  (IAGP)
Atrial septal defect  (IAGP)
Attention deficit hyperactivity disorder  (IAGP)
Autistic behavior  (IAGP)
Autosomal dominant inheritance  (IAGP)
Bicuspid aortic valve  (IAGP)
Bladder diverticulum  (IAGP)
Blepharophimosis  (IAGP)
Blue irides  (IAGP)
Broad nasal tip  (IAGP)
Celiac disease  (IAGP)
Cerebellar hypoplasia  (IAGP)
Chronic constipation  (IAGP)
Clinodactyly of the 5th finger  (IAGP)
Colonic diverticula  (IAGP)
Constipation  (IAGP)
Coronary artery stenosis  (IAGP)
Cutis laxa  (IAGP)
Dental malocclusion  (IAGP)
Depressed nasal bridge  (IAGP)
Diabetes mellitus  (IAGP)
Down-sloping shoulders  (IAGP)
Early onset of sexual maturation  (IAGP)
Enuresis  (IAGP)
Epicanthus  (IAGP)
Failure to thrive in infancy  (IAGP)
Feeding difficulties in infancy  (IAGP)
Flexion contracture  (IAGP)
Food intolerance  (IAGP)
Full cheeks  (IAGP)
Gait imbalance  (IAGP)
Gastroesophageal reflux  (IAGP)
Generalized hypotonia  (IAGP)
Glucose intolerance  (IAGP)
Hallux valgus  (IAGP)
Hoarse voice  (IAGP)
Hyperacusis  (IAGP)
Hypercalcemia  (IAGP)
Hypercalciuria  (IAGP)
Hyperreflexia  (IAGP)
Hypertension  (IAGP)
Hypodontia  (IAGP)
Hypotelorism  (IAGP)
Hypothyroidism  (IAGP)
Hypotonia  (IAGP)
Impaired visuospatial constructive cognition  (IAGP)
Incoordination  (IAGP)
Inguinal hernia  (IAGP)
Intellectual disability  (IAGP)
Intestinal malrotation  (IAGP)
Intrauterine growth retardation  (IAGP)
Joint laxity  (IAGP)
Kyphoscoliosis  (IAGP)
Large earlobe  (IAGP)
Long philtrum  (IAGP)
Malar flattening  (IAGP)
Medial flaring of the eyebrow  (IAGP)
Microdontia  (IAGP)
Micropenis  (IAGP)
Midface retrusion  (IAGP)
Mitral regurgitation  (IAGP)
Myxomatous mitral valve degeneration  (IAGP)
Narrow forehead  (IAGP)
Nephrocalcinosis  (IAGP)
Obesity  (IAGP)
Obsessive-compulsive trait  (IAGP)
Open mouth  (IAGP)
Osteopenia  (IAGP)
Osteoporosis  (IAGP)
Pectus excavatum  (IAGP)
Pelvic kidney  (IAGP)
Periorbital fullness  (IAGP)
Peripheral pulmonary artery stenosis  (IAGP)
Phonophobia  (IAGP)
Poor coordination  (IAGP)
Portal hypertension  (IAGP)
Premature graying of hair  (IAGP)
Pulmonic stenosis  (IAGP)
Radioulnar synostosis  (IAGP)
Rectal prolapse  (IAGP)
Recurrent otitis media  (IAGP)
Recurrent urinary tract infections  (IAGP)
Renal artery stenosis  (IAGP)
Renal hypoplasia  (IAGP)
Renal insufficiency  (IAGP)
Retinal arteriolar tortuosity  (IAGP)
Schizophrenia  (IAGP)
Sensorineural hearing impairment  (IAGP)
Short nose  (IAGP)
Short stature  (IAGP)
Sleep disturbance  (IAGP)
Small nail  (IAGP)
Soft skin  (IAGP)
Strabismus  (IAGP)
Stroke  (IAGP)
Sudden death  (IAGP)
Supravalvular aortic stenosis  (IAGP)
Thick lower lip vermilion  (IAGP)
Umbilical hernia  (IAGP)
Urethral stenosis  (IAGP)
Ventricular septal defect  (IAGP)
Vesicoureteral reflux  (IAGP)
Vocal cord paralysis  (IAGP)
References

Additional References at PubMed
PMID:9860302   PMID:10593926   PMID:11230181   PMID:11698644   PMID:12477932   PMID:12721358   PMID:14702039   PMID:14742444   PMID:14759258   PMID:15163635   PMID:15489334   PMID:16644671  
PMID:18193043   PMID:18193044   PMID:18193046   PMID:18591247   PMID:18606808   PMID:18946681   PMID:18950580   PMID:19060906   PMID:19060911   PMID:19148283   PMID:19252981   PMID:19274049  
PMID:19487539   PMID:19571538   PMID:19680233   PMID:19913121   PMID:19995986   PMID:20025850   PMID:20158509   PMID:20167577   PMID:20301427   PMID:20382893   PMID:20570916   PMID:20580033  
PMID:20657596   PMID:20679960   PMID:20686565   PMID:20864672   PMID:20965718   PMID:20972250   PMID:21036147   PMID:21145868   PMID:21282101   PMID:21665952   PMID:21726544   PMID:21811631  
PMID:21835137   PMID:21840420   PMID:21873635   PMID:21909109   PMID:21938000   PMID:21988832   PMID:22001757   PMID:22286219   PMID:22338092   PMID:22399527   PMID:22466288   PMID:22546860  
PMID:23209190   PMID:23263486   PMID:23443556   PMID:23505323   PMID:23530060   PMID:23597489   PMID:23604004   PMID:23756994   PMID:23803610   PMID:24055811   PMID:24097068   PMID:24366300  
PMID:24448738   PMID:24449882   PMID:24616092   PMID:24664750   PMID:24845031   PMID:24989072   PMID:25111846   PMID:25288136   PMID:25332233   PMID:25573592   PMID:26124292   PMID:26147751  
PMID:26177557   PMID:26384380   PMID:26526060   PMID:26638075   PMID:26673895   PMID:26760575   PMID:26910886   PMID:27029511   PMID:27033449   PMID:27281235   PMID:27599772   PMID:27669460  
PMID:27854512   PMID:27919710   PMID:28027934   PMID:28065597   PMID:28123933   PMID:28514442   PMID:28606928   PMID:28768172   PMID:29153407   PMID:29509190   PMID:29764859   PMID:29844126  
PMID:29858861   PMID:30079502   PMID:30420491   PMID:30804502   PMID:31227231   PMID:31407220   PMID:31409643   PMID:31413120   PMID:31782782   PMID:32129710   PMID:32694731   PMID:32776146  
PMID:33320482  


Genomics

Comparative Map Data
MLXIPL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl773,593,194 - 73,624,543 (-)EnsemblGRCh38hg38GRCh38
GRCh38773,593,201 - 73,624,522 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37773,007,532 - 73,038,852 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36772,645,460 - 72,676,806 (-)NCBINCBI36hg18NCBI36
Build 34772,452,174 - 72,483,521NCBI
Celera768,485,730 - 68,517,088 (-)NCBI
Cytogenetic Map7q11.23NCBI
HuRef768,888,586 - 68,920,882 (-)NCBIHuRef
CHM1_1773,153,232 - 73,184,535 (-)NCBICHM1_1
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)NCBI
Mlxipl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395135,118,744 - 135,168,622 (+)NCBIGRCm39mm39
GRCm39 Ensembl5135,118,744 - 135,167,236 (+)Ensembl
GRCm385135,089,890 - 135,139,768 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5135,089,890 - 135,138,382 (+)EnsemblGRCm38mm10GRCm38
MGSCv375135,582,783 - 135,613,792 (+)NCBIGRCm37mm9NCBIm37
MGSCv365135,391,540 - 135,426,429 (+)NCBImm8
Celera5132,118,107 - 132,149,116 (+)NCBICelera
Cytogenetic Map5G2NCBI
Mlxipl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21221,542,964 - 21,577,120 (-)NCBI
Rnor_6.01224,590,645 - 24,619,639 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01226,588,220 - 26,620,779 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera1223,305,691 - 23,340,439 (-)NCBICelera
Cytogenetic Map12q12NCBI
Mlxipl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545614,096,531 - 14,117,269 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545614,096,530 - 14,116,687 (+)NCBIChiLan1.0ChiLan1.0
MLXIPL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1780,745,765 - 80,776,156 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl780,745,765 - 80,776,153 (-)Ensemblpanpan1.1panPan2
MLXIPL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.166,617,398 - 6,652,201 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl66,633,231 - 6,652,198 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha68,314,804 - 8,349,596 (+)NCBI
ROS_Cfam_1.066,448,811 - 6,467,272 (+)NCBI
UMICH_Zoey_3.166,421,940 - 6,456,726 (+)NCBI
UNSW_CanFamBas_1.066,369,681 - 6,404,478 (+)NCBI
UU_Cfam_GSD_1.066,533,405 - 6,568,214 (+)NCBI
Mlxipl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344131,163,797 - 131,197,462 (+)NCBI
SpeTri2.0NW_0049365432,839,105 - 2,856,997 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MLXIPL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl310,894,270 - 10,934,047 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1310,898,675 - 10,934,257 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2310,598,366 - 10,632,610 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MLXIPL
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1289,442,520 - 9,465,772 (+)NCBI
Mlxipl
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474014,150,425 - 14,187,687 (+)NCBI

Position Markers
D7S2476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,015,454 - 73,015,601UniSTSGRCh37
GRCh37773,015,457 - 73,016,136UniSTSGRCh37
GRCh37773,015,457 - 73,015,667UniSTSGRCh37
Build 36772,653,390 - 72,653,537RGDNCBI36
Celera768,493,659 - 68,493,816RGD
Celera768,493,662 - 68,494,351UniSTS
Celera768,493,662 - 68,493,882UniSTS
Cytogenetic Map7q11.23UniSTS
HuRef768,896,517 - 68,896,692UniSTS
HuRef768,896,514 - 68,896,626UniSTS
HuRef768,896,517 - 68,897,161UniSTS
CRA_TCAGchr7v2772,348,526 - 72,348,673UniSTS
CRA_TCAGchr7v2772,348,529 - 72,348,739UniSTS
CRA_TCAGchr7v2772,348,529 - 72,349,208UniSTS
Marshfield Genetic Map784.52UniSTS
Marshfield Genetic Map784.52RGD
Genethon Genetic Map784.4UniSTS
deCODE Assembly Map785.41UniSTS
RH64919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,007,700 - 73,007,833UniSTSGRCh37
Build 36772,645,636 - 72,645,769RGDNCBI36
Celera768,485,906 - 68,486,039RGD
Cytogenetic Map7q11.23UniSTS
HuRef768,888,762 - 68,888,895UniSTS
CRA_TCAGchr7v2772,340,772 - 72,340,905UniSTS
GeneMap99-GB4 RH Map7423.57UniSTS
NCBI RH Map7894.5UniSTS
G60573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,015,464 - 73,015,589UniSTSGRCh37
Build 36772,653,400 - 72,653,525RGDNCBI36
Celera768,493,669 - 68,493,804RGD
Cytogenetic Map7q11.23UniSTS
HuRef768,896,524 - 68,896,614UniSTS
CRA_TCAGchr7v2772,348,536 - 72,348,661UniSTS
TNG Radiation Hybrid Map282319.0UniSTS
D7S809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,016,357 - 73,016,613UniSTSGRCh37
Build 36772,654,293 - 72,654,549RGDNCBI36
Celera768,494,572 - 68,494,832RGD
Cytogenetic Map7q11.23UniSTS
HuRef768,897,382 - 68,898,307UniSTS
CRA_TCAGchr7v2772,349,429 - 72,349,685UniSTS
SHGC-107367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,035,549 - 73,035,830UniSTSGRCh37
Build 36772,673,485 - 72,673,766RGDNCBI36
Celera768,513,767 - 68,514,048RGD
Cytogenetic Map7q11.23UniSTS
HuRef768,917,251 - 68,917,532UniSTS
CRA_TCAGchr7v2772,368,621 - 72,368,902UniSTS
D7S1624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,032,197 - 73,032,292UniSTSGRCh37
Build 36772,670,133 - 72,670,228RGDNCBI36
Celera768,510,415 - 68,510,510RGD
Cytogenetic Map7q11.23UniSTS
HuRef768,913,902 - 68,913,997UniSTS
CRA_TCAGchr7v2772,365,269 - 72,365,364UniSTS
D7S2523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,023,812 - 73,024,083UniSTSGRCh37
Build 36772,661,748 - 72,662,019RGDNCBI36
Celera768,502,030 - 68,502,301RGD
HuRef768,905,516 - 68,905,787UniSTS
CRA_TCAGchr7v2772,356,884 - 72,357,155UniSTS
Wbscr14  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37773,008,219 - 73,008,655UniSTSGRCh37
Build 36772,646,155 - 72,646,591RGDNCBI36
Celera768,486,425 - 68,486,861RGD
HuRef768,889,281 - 68,889,717UniSTS
CRA_TCAGchr7v2772,341,291 - 72,341,727UniSTS
D10S16   No map positions available.
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
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Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS
D7S2476  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q11.23UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5254
Count of miRNA genes:930
Interacting mature miRNAs:1172
Transcripts:ENST00000313375, ENST00000345114, ENST00000354613, ENST00000395189, ENST00000414749, ENST00000429400, ENST00000434326, ENST00000453275, ENST00000456640, ENST00000467221, ENST00000476404, ENST00000488212
Prediction methods:Microtar, Miranda, Rnahybrid
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.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1 1 1
Medium 985 202 1374 516 174 439 2024 1164 2161 191 593 547 78 1186 1181
Low 1432 1641 334 103 270 21 1920 898 1492 186 755 973 92 1 18 1273 2 2
Below cutoff 17 1135 16 4 1101 4 406 133 78 37 105 88 4 333 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_009307 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_134541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001744799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC005089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF156603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF156673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF245470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF245471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF245472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF245473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF245474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG772360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ480402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ515858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC853060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC853061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC853062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF306322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF306323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF306324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000313375   ⟹   ENSP00000320886
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,202 - 73,624,522 (-)Ensembl
RefSeq Acc Id: ENST00000345114   ⟹   ENSP00000343767
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,194 - 73,624,492 (-)Ensembl
RefSeq Acc Id: ENST00000354613   ⟹   ENSP00000346629
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,194 - 73,624,540 (-)Ensembl
RefSeq Acc Id: ENST00000414749   ⟹   ENSP00000412330
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,194 - 73,624,492 (-)Ensembl
RefSeq Acc Id: ENST00000429400   ⟹   ENSP00000406296
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,194 - 73,624,492 (-)Ensembl
RefSeq Acc Id: ENST00000434326   ⟹   ENSP00000392636
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,593,202 - 73,624,514 (-)Ensembl
RefSeq Acc Id: ENST00000453275   ⟹   ENSP00000395172
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,597,645 - 73,624,543 (-)Ensembl
RefSeq Acc Id: ENST00000456640   ⟹   ENSP00000402615
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,605,910 - 73,616,161 (-)Ensembl
RefSeq Acc Id: ENST00000467221
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,596,174 - 73,597,362 (-)Ensembl
RefSeq Acc Id: ENST00000476404
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,596,710 - 73,606,824 (-)Ensembl
RefSeq Acc Id: ENST00000488212
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl773,599,592 - 73,607,120 (-)Ensembl
RefSeq Acc Id: NM_032951   ⟹   NP_116569
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,202 - 73,624,522 (-)NCBI
GRCh37773,007,524 - 73,038,903 (-)NCBI
Build 36772,645,460 - 72,676,806 (-)NCBI Archive
HuRef768,888,586 - 68,920,882 (-)ENTREZGENE
CHM1_1773,153,232 - 73,184,532 (-)NCBI
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_032952   ⟹   NP_116570
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,202 - 73,624,522 (-)NCBI
GRCh37773,007,524 - 73,038,903 (-)NCBI
Build 36772,645,460 - 72,676,806 (-)NCBI Archive
HuRef768,888,586 - 68,920,882 (-)ENTREZGENE
CHM1_1773,153,232 - 73,184,532 (-)NCBI
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_032953   ⟹   NP_116571
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,202 - 73,624,522 (-)NCBI
GRCh37773,007,524 - 73,038,903 (-)NCBI
Build 36772,645,460 - 72,676,806 (-)NCBI Archive
HuRef768,888,586 - 68,920,882 (-)ENTREZGENE
CHM1_1773,153,232 - 73,184,532 (-)NCBI
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_032954   ⟹   NP_116572
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,202 - 73,624,522 (-)NCBI
GRCh37773,007,524 - 73,038,903 (-)NCBI
Build 36772,645,460 - 72,676,806 (-)NCBI Archive
HuRef768,888,586 - 68,920,882 (-)ENTREZGENE
CHM1_1773,153,232 - 73,184,532 (-)NCBI
CRA_TCAGchr7v2772,340,596 - 72,371,942 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NR_134541
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,202 - 73,624,522 (-)NCBI
CHM1_1773,153,232 - 73,184,535 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516277   ⟹   XP_011514579
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,624,522 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516278   ⟹   XP_011514580
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,624,522 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516279   ⟹   XP_011514581
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,624,522 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516281   ⟹   XP_011514583
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,604,017 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012263   ⟹   XP_016867752
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,606,002 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446784   ⟹   XP_024302552
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,604,018 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001744799
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,593,201 - 73,624,522 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_116569 (Get FASTA)   NCBI Sequence Viewer  
  NP_116570 (Get FASTA)   NCBI Sequence Viewer  
  NP_116571 (Get FASTA)   NCBI Sequence Viewer  
  NP_116572 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514579 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514580 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514581 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514583 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867752 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302552 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF68174 (Get FASTA)   NCBI Sequence Viewer  
  AAF68176 (Get FASTA)   NCBI Sequence Viewer  
  AAH12925 (Get FASTA)   NCBI Sequence Viewer  
  AAK20935 (Get FASTA)   NCBI Sequence Viewer  
  AAK20936 (Get FASTA)   NCBI Sequence Viewer  
  AAK20937 (Get FASTA)   NCBI Sequence Viewer  
  AAK20938 (Get FASTA)   NCBI Sequence Viewer  
  AAK20939 (Get FASTA)   NCBI Sequence Viewer  
  ACS13745 (Get FASTA)   NCBI Sequence Viewer  
  ACS13746 (Get FASTA)   NCBI Sequence Viewer  
  ACS13747 (Get FASTA)   NCBI Sequence Viewer  
  ACS13748 (Get FASTA)   NCBI Sequence Viewer  
  AGR34141 (Get FASTA)   NCBI Sequence Viewer  
  AGR34142 (Get FASTA)   NCBI Sequence Viewer  
  AGR34143 (Get FASTA)   NCBI Sequence Viewer  
  EAW69660 (Get FASTA)   NCBI Sequence Viewer  
  EAW69661 (Get FASTA)   NCBI Sequence Viewer  
  EAW69663 (Get FASTA)   NCBI Sequence Viewer  
  EAW69668 (Get FASTA)   NCBI Sequence Viewer  
  Q9NP71 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_116572   ⟸   NM_032954
- Peptide Label: isoform delta
- UniProtKB: Q9NP71 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_116571   ⟸   NM_032953
- Peptide Label: isoform gamma
- UniProtKB: Q9NP71 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_116570   ⟸   NM_032952
- Peptide Label: isoform beta
- UniProtKB: Q9NP71 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_116569   ⟸   NM_032951
- Peptide Label: isoform alpha
- UniProtKB: Q9NP71 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011514580   ⟸   XM_011516278
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011514581   ⟸   XM_011516279
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011514579   ⟸   XM_011516277
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011514583   ⟸   XM_011516281
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016867752   ⟸   XM_017012263
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_024302552   ⟸   XM_024446784
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: ENSP00000343767   ⟸   ENST00000345114
RefSeq Acc Id: ENSP00000412330   ⟸   ENST00000414749
RefSeq Acc Id: ENSP00000395172   ⟸   ENST00000453275
RefSeq Acc Id: ENSP00000406296   ⟸   ENST00000429400
RefSeq Acc Id: ENSP00000402615   ⟸   ENST00000456640
RefSeq Acc Id: ENSP00000320886   ⟸   ENST00000313375
RefSeq Acc Id: ENSP00000346629   ⟸   ENST00000354613
RefSeq Acc Id: ENSP00000392636   ⟸   ENST00000434326
Protein Domains
bHLH

Promoters
RGD ID:6805924
Promoter ID:HG_KWN:57964
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562
Transcripts:OTTHUMT00000347604,   OTTHUMT00000347607
Position:
Human AssemblyChrPosition (strand)Source
Build 36772,659,221 - 72,659,721 (-)MPROMDB
RGD ID:6805925
Promoter ID:HG_KWN:57966
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562
Transcripts:ENST00000345114,   ENST00000395189,   NM_032951,   NM_032952,   NM_032953,   NM_032954,   OTTHUMT00000347605,   UC003TYP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36772,676,474 - 72,676,974 (-)MPROMDB
RGD ID:7210769
Promoter ID:EPDNEW_H11130
Type:initiation region
Name:MLXIPL_1
Description:MLX interacting protein like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38773,624,522 - 73,624,582EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q11.22-21.11(chr7:71225344-81735657)x1 copy number loss See cases [RCV000050709] Chr7:71225344..81735657 [GRCh38]
Chr7:70690330..81364973 [GRCh37]
Chr7:70328266..81202909 [NCBI36]
Chr7:7q11.22-21.11
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74719013)x3 copy number gain See cases [RCV000050379] Chr7:73352304..74719013 [GRCh38]
Chr7:72766313..74133332 [GRCh37]
Chr7:72404249..73771268 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74719013)x1 copy number loss See cases [RCV000050382] Chr7:73352304..74719013 [GRCh38]
Chr7:72766313..74133332 [GRCh37]
Chr7:72404249..73771268 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74924037)x1 copy number loss See cases [RCV000051134] Chr7:73352304..74924037 [GRCh38]
Chr7:72766313..74339044 [GRCh37]
Chr7:72404249..73976980 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:72930548-74869255)x1 copy number loss See cases [RCV000050996] Chr7:72930548..74869255 [GRCh38]
Chr7:72401086..74285345 [GRCh37]
Chr7:72039022..73923281 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74869255)x1 copy number loss See cases [RCV000050999] Chr7:73352304..74869255 [GRCh38]
Chr7:72766313..74285345 [GRCh37]
Chr7:72404249..73923281 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.21-21.11(chr7:64560824-79186156)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052318]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052318]|See cases [RCV000052318] Chr7:64560824..79186156 [GRCh38]
Chr7:64021202..78815472 [GRCh37]
Chr7:63658637..78653408 [NCBI36]
Chr7:7q11.21-21.11
pathogenic
GRCh38/hg38 7q11.22-11.23(chr7:68668307-73710276)x1 copy number loss See cases [RCV000052321] Chr7:68668307..73710276 [GRCh38]
Chr7:68133294..72806397 [GRCh37]
Chr7:67771230..72762542 [NCBI36]
Chr7:7q11.22-11.23
pathogenic
GRCh38/hg38 7q11.22-11.23(chr7:72649515-75361855)x3 copy number gain See cases [RCV000051965] Chr7:72649515..75361855 [GRCh38]
Chr7:72196405..74991125 [GRCh37]
Chr7:71752436..74829061 [NCBI36]
Chr7:7q11.22-11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:72768821-74869255)x3 copy number gain See cases [RCV000051966] Chr7:72768821..74869255 [GRCh38]
Chr7:72233835..74285345 [GRCh37]
Chr7:71871771..73923281 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74725240)x3 copy number gain See cases [RCV000051967] Chr7:73280574..74725240 [GRCh38]
Chr7:72665462..74139573 [GRCh37]
Chr7:72303398..73777509 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74725240)x3 copy number gain See cases [RCV000051986] Chr7:73280574..74725240 [GRCh38]
Chr7:72679397..74139573 [GRCh37]
Chr7:72317333..73777509 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74839100)x3 copy number gain See cases [RCV000051989] Chr7:73280574..74839100 [GRCh38]
Chr7:72683244..74267189 [GRCh37]
Chr7:72321180..73905125 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73312575-74723034)x3 copy number gain See cases [RCV000051990] Chr7:73312575..74723034 [GRCh38]
Chr7:72726571..74137354 [GRCh37]
Chr7:72364507..73775290 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352104-74924178)x3 copy number gain See cases [RCV000051991] Chr7:73352104..74924178 [GRCh38]
Chr7:72766113..74339185 [GRCh37]
Chr7:72404049..73977121 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q11.23(chr7:73096542-74727989)x1 copy number loss See cases [RCV000053133] Chr7:73096542..74727989 [GRCh38]
Chr7:72507129..74142327 [GRCh37]
Chr7:72145065..73780263 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74723034)x1 copy number loss See cases [RCV000053143] Chr7:73280574..74723034 [GRCh38]
Chr7:72681397..74137354 [GRCh37]
Chr7:72319333..73775290 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74723034)x1 copy number loss See cases [RCV000053144] Chr7:73286412..74723034 [GRCh38]
Chr7:72700414..74137354 [GRCh37]
Chr7:72338350..73775290 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74725240)x3 copy number gain See cases [RCV000053146] Chr7:73286412..74725240 [GRCh38]
Chr7:72700414..74139573 [GRCh37]
Chr7:72338350..73777509 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74725240)x1 copy number loss See cases [RCV000053147] Chr7:73286412..74725240 [GRCh38]
Chr7:72700414..74139573 [GRCh37]
Chr7:72338350..73777509 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74707848)x1 copy number loss See cases [RCV000053150] Chr7:73286412..74707848 [GRCh38]
Chr7:72700414..74122179 [GRCh37]
Chr7:72338350..73760115 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352104-74719154)x3 copy number gain See cases [RCV000053151] Chr7:73352104..74719154 [GRCh38]
Chr7:72766113..74133473 [GRCh37]
Chr7:72404049..73771409 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352104-74719154)x1 copy number loss See cases [RCV000053152] Chr7:73352104..74719154 [GRCh38]
Chr7:72766113..74133473 [GRCh37]
Chr7:72404049..73771409 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.22-11.23(chr7:69382353-77823832)x1 copy number loss See cases [RCV000054111] Chr7:69382353..77823832 [GRCh38]
Chr7:68847339..77453149 [GRCh37]
Chr7:68485275..77291085 [NCBI36]
Chr7:7q11.22-11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74133404)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054116]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054116]|See cases [RCV000054116] Chr7:73352304..74133404 [GRCh38]
Chr7:72404249..73185670 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73614671-73942928)x1 copy number loss See cases [RCV000054117] Chr7:73614671..73942928 [GRCh38]
Chr7:72666937..72995194 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-76722261)x1 copy number loss See cases [RCV000133638] Chr7:73352304..76722261 [GRCh38]
Chr7:72766313..76351578 [GRCh37]
Chr7:72404249..76189514 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73304255-74718954)x1 copy number loss See cases [RCV000134329] Chr7:73304255..74718954 [GRCh38]
Chr7:72718252..74133273 [GRCh37]
Chr7:72356188..73771209 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q11.22-11.23(chr7:71461127-73614730)x1 copy number loss See cases [RCV000135816] Chr7:71461127..73614730 [GRCh38]
Chr7:70926112..72806397 [GRCh37]
Chr7:70564048..72666996 [NCBI36]
Chr7:7q11.22-11.23
pathogenic|likely pathogenic
GRCh38/hg38 7q11.23(chr7:73040501-75255046)x3 copy number gain See cases [RCV000135712] Chr7:73040501..75255046 [GRCh38]
Chr7:74285295..76351578 [GRCh37]
Chr7:73923231..76189514 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.23(chr7:72938064-74779028)x3 copy number gain See cases [RCV000136287] Chr7:72938064..74779028 [GRCh38]
Chr7:72408602..74193374 [GRCh37]
Chr7:72046538..73831310 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74924007)x1 copy number loss See cases [RCV000136391] Chr7:73280574..74924007 [GRCh38]
Chr7:72636006..74339014 [GRCh37]
Chr7:72273942..73976950 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352303-74719008)x3 copy number gain See cases [RCV000136042] Chr7:73352303..74719008 [GRCh38]
Chr7:72766312..74133327 [GRCh37]
Chr7:72404248..73771263 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352303-74719008)x1 copy number loss See cases [RCV000136046] Chr7:73352303..74719008 [GRCh38]
Chr7:72766312..74133327 [GRCh37]
Chr7:72404248..73771263 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352303-74924023)x1 copy number loss See cases [RCV000136076] Chr7:73352303..74924023 [GRCh38]
Chr7:72766312..74339030 [GRCh37]
Chr7:72404248..73976966 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352303-74779051)x1 copy number loss See cases [RCV000136014] Chr7:73352303..74779051 [GRCh38]
Chr7:72766312..74193397 [GRCh37]
Chr7:72404248..73831333 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73312582-74725057)x1 copy number loss See cases [RCV000136793] Chr7:73312582..74725057 [GRCh38]
Chr7:72726578..74139390 [GRCh37]
Chr7:72364514..73777326 [NCBI36]
Chr7:7q11.23
pathogenic
NM_032951.3(MLXIPL):c.1372A>C (p.Thr458Pro) single nucleotide variant not specified [RCV000202729] Chr7:73597413 [GRCh38]
Chr7:73011743 [GRCh37]
Chr7:7q11.23
benign
GRCh38/hg38 7q11.23(chr7:73192369-74779057)x3 copy number gain See cases [RCV000138102] Chr7:73192369..74779057 [GRCh38]
Chr7:72606409..74193403 [GRCh37]
Chr7:72244345..73831339 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73192369-74779057)x1 copy number loss See cases [RCV000138103] Chr7:73192369..74779057 [GRCh38]
Chr7:72606409..74193403 [GRCh37]
Chr7:72244345..73831339 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73040501-75255046)x3 copy number gain See cases [RCV000137731] Chr7:73040501..75255046 [GRCh38]
Chr7:72635638..74904285 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74727989)x1 copy number loss See cases [RCV000138355] Chr7:73286412..74727989 [GRCh38]
Chr7:72700414..74142327 [GRCh37]
Chr7:72338350..73780263 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74727989)x3 copy number gain See cases [RCV000138356] Chr7:73280574..74727989 [GRCh38]
Chr7:72685734..74142327 [GRCh37]
Chr7:72323670..73780263 [NCBI36]
Chr7:7q11.23
pathogenic|conflicting data from submitters
GRCh38/hg38 7q11.23(chr7:73271690-74727989)x1 copy number loss See cases [RCV000138357] Chr7:73271690..74727989 [GRCh38]
Chr7:72685734..74142327 [GRCh37]
Chr7:72323670..73780263 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73192369-74869255)x1 copy number loss See cases [RCV000139190] Chr7:73192369..74869255 [GRCh38]
Chr7:72606409..74285345 [GRCh37]
Chr7:72244345..73923281 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74779057)x3 copy number gain See cases [RCV000139121] Chr7:73280574..74779057 [GRCh38]
Chr7:72663962..74193403 [GRCh37]
Chr7:72301898..73831339 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74869255)x1 copy number loss See cases [RCV000139797] Chr7:73286412..74869255 [GRCh38]
Chr7:72700414..74285345 [GRCh37]
Chr7:72338350..73923281 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74779057)x1 copy number loss See cases [RCV000140662] Chr7:73286412..74779057 [GRCh38]
Chr7:72700414..74193403 [GRCh37]
Chr7:72338350..73831339 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73192369-74883978)x3 copy number gain See cases [RCV000140718] Chr7:73192369..74883978 [GRCh38]
Chr7:72606409..74300084 [GRCh37]
Chr7:72244345..73938020 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73175475-74740268)x3 copy number gain See cases [RCV000141703] Chr7:73175475..74740268 [GRCh38]
Chr7:72589515..74154603 [GRCh37]
Chr7:72227451..73792539 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286125-74732517)x3 copy number gain See cases [RCV000142341] Chr7:73286125..74732517 [GRCh38]
Chr7:72700127..74146858 [GRCh37]
Chr7:72338063..73784794 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74789341)x1 copy number loss See cases [RCV000142414] Chr7:73280574..74789341 [GRCh38]
Chr7:72637824..74203685 [GRCh37]
Chr7:72275760..73841621 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.21-11.23(chr7:62977085-75415352)x3 copy number gain See cases [RCV000142242] Chr7:62977085..75415352 [GRCh38]
Chr7:62437463..75044630 [GRCh37]
Chr7:62074898..74882566 [NCBI36]
Chr7:7q11.21-11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286508-74727852)x1 copy number loss See cases [RCV000142230] Chr7:73286508..74727852 [GRCh38]
Chr7:72700510..74142190 [GRCh37]
Chr7:72338446..73780126 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74727918)x1 copy number loss See cases [RCV000142156] Chr7:73280574..74727918 [GRCh38]
Chr7:72650120..74142256 [GRCh37]
Chr7:72288056..73780192 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286522-74727156)x1 copy number loss See cases [RCV000142159] Chr7:73286522..74727156 [GRCh38]
Chr7:72700524..74141494 [GRCh37]
Chr7:72338460..73779430 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73286412-74758583)x1 copy number loss See cases [RCV000142891] Chr7:73286412..74758583 [GRCh38]
Chr7:72700414..74172913 [GRCh37]
Chr7:72338350..73810849 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-75065728)x3 copy number gain See cases [RCV000142690] Chr7:73352304..75065728 [GRCh38]
Chr7:72766313..74481540 [GRCh37]
Chr7:72404249..74119476 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.21-11.23(chr7:62736364-75432710)x1 copy number loss See cases [RCV000142528] Chr7:62736364..75432710 [GRCh38]
Chr7:62196742..75061986 [GRCh37]
Chr7:61834177..74899922 [NCBI36]
Chr7:7q11.21-11.23
pathogenic
GRCh38/hg38 7q11.22-21.11(chr7:72179092-79164071) copy number gain See cases [RCV000143454] Chr7:72179092..79164071 [GRCh38]
Chr7:71644077..78793387 [GRCh37]
Chr7:71282013..78631323 [NCBI36]
Chr7:7q11.22-21.11
likely pathogenic
GRCh38/hg38 7q11.23(chr7:73280574-74728722)x3 copy number gain See cases [RCV000143390] Chr7:73280574..74728722 [GRCh38]
Chr7:72677301..74143060 [GRCh37]
Chr7:72315237..73780996 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74719013)x3 copy number gain See cases [RCV000148080] Chr7:73352304..74719013 [GRCh38]
Chr7:72766313..74133332 [GRCh37]
Chr7:72404249..73771268 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74924037)x1 copy number loss See cases [RCV000148081] Chr7:73352304..74924037 [GRCh38]
Chr7:72766313..74339044 [GRCh37]
Chr7:72404249..73976980 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73304280-74727852)x1 copy number loss See cases [RCV000143632] Chr7:73304280..74727852 [GRCh38]
Chr7:72718277..74142190 [GRCh37]
Chr7:72356213..73780126 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-74719013)x1 copy number loss See cases [RCV000148142] Chr7:73352304..74719013 [GRCh38]
Chr7:72766313..74133332 [GRCh37]
Chr7:72404249..73771268 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718252-74133332)x1 copy number loss See cases [RCV000239835] Chr7:72718252..74133332 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72708237-74339044)x1 copy number loss See cases [RCV000239823] Chr7:72708237..74339044 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72722981-74217390)x1 copy number loss See cases [RCV000258813] Chr7:72722981..74217390 [GRCh37]
Chr7:7q11.23
pathogenic|likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72722981-74141840)x1 copy number loss See cases [RCV000207450] Chr7:72722981..74141840 [GRCh37]
Chr7:7q11.23
pathogenic
Single allele duplication Autism spectrum disorder [RCV000225382] Chr7:72718278..74140708 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.22-11.23(chr7:71968212-74133332)x3 copy number gain See cases [RCV000240527] Chr7:71968212..74133332 [GRCh37]
Chr7:7q11.22-11.23
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72713253-74142256)x1 copy number loss See cases [RCV000449356] Chr7:72713253..74142256 [GRCh37]
Chr7:7q11.23
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141673)x1 copy number loss See cases [RCV000449372] Chr7:72718277..74141673 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72700127-74143240)x3 copy number gain See cases [RCV000446793] Chr7:72700127..74143240 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72713253-74143030)x1 copy number loss See cases [RCV000447530] Chr7:72713253..74143030 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74142190)x1 copy number loss See cases [RCV000447273] Chr7:72718277..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72708237-74133273)x1 copy number loss See cases [RCV000446832] Chr7:72708237..74133273 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72686958-74142190)x3 copy number gain See cases [RCV000446236] Chr7:72686958..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141603)x1 copy number loss See cases [RCV000447620] Chr7:72718277..74141603 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74146948)x1 copy number loss See cases [RCV000446172] Chr7:72718277..74146948 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74142215)x1 copy number loss See cases [RCV000447454] Chr7:72718277..74142215 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72692112-74141746)x3 copy number gain See cases [RCV000445755] Chr7:72692112..74141746 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72700524-74142190)x1 copy number loss See cases [RCV000447774] Chr7:72700524..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141784)x1 copy number loss See cases [RCV000448046] Chr7:72718277..74141784 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718123-74141746)x1 copy number loss See cases [RCV000448666] Chr7:72718123..74141746 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72472922-74259176)x3 copy number gain See cases [RCV000448344] Chr7:72472922..74259176 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72700524-74142256)x3 copy number gain See cases [RCV000512105] Chr7:72700524..74142256 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72722981-73198616)x1 copy number loss See cases [RCV000515566] Chr7:72722981..73198616 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:72643631-74142190)x1 copy number loss See cases [RCV000512130] Chr7:72643631..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72677301-74143240)x3 copy number gain See cases [RCV000512048] Chr7:72677301..74143240 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74287433)x1 copy number loss See cases [RCV000510195] Chr7:72718277..74287433 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74259899)x1 copy number loss See cases [RCV000510198] Chr7:72718277..74259899 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72701018-74141493)x1 copy number loss See cases [RCV000510144] Chr7:72701018..74141493 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72691242-74142190)x1 copy number loss See cases [RCV000510243] Chr7:72691242..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-73898515)x1 copy number loss See cases [RCV000511510] Chr7:72718277..73898515 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74146858)x1 copy number loss See cases [RCV000511528] Chr7:72718277..74146858 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72692112-74154497)x3 copy number gain See cases [RCV000511487] Chr7:72692112..74154497 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141494)x1 copy number loss See cases [RCV000511955] Chr7:72718277..74141494 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72677173-74143140)x3 copy number gain See cases [RCV000510884] Chr7:72677173..74143140 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141603)x1 copy number loss See cases [RCV000511254] Chr7:72718277..74141603 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72589515-74165401)x3 copy number gain See cases [RCV000510938] Chr7:72589515..74165401 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72456604-76007380)x1 copy number loss See cases [RCV000510782] Chr7:72456604..76007380 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72721449-73959106) copy number loss Williams syndrome [RCV000767559] Chr7:72721449..73959106 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72772522-74133319) copy number loss Short stature [RCV000626538] Chr7:72772522..74133319 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72766313-74133332) copy number loss Global developmental delay [RCV000626537] Chr7:72766313..74133332 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718277-74141746)x1 copy number loss See cases [RCV000512220] Chr7:72718277..74141746 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72536980-74629034)x1 copy number loss See cases [RCV000512310] Chr7:72536980..74629034 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72577021-74197846)x3 copy number gain See cases [RCV000512328] Chr7:72577021..74197846 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72659674-74143240)x3 copy number gain See cases [RCV000512332] Chr7:72659674..74143240 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72686958-73113924)x3 copy number gain not provided [RCV000682843] Chr7:72686958..73113924 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:72700524-74069858)x3 copy number gain not provided [RCV000682883] Chr7:72700524..74069858 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72612042-74574641)x1 copy number loss not provided [RCV000682895] Chr7:72612042..74574641 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72718123-74141784)x1 copy number loss not provided [RCV000682885] Chr7:72718123..74141784 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72577021-74859638)x3 copy number gain not provided [RCV000682898] Chr7:72577021..74859638 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72576872-74175429)x3 copy number gain not provided [RCV000682888] Chr7:72576872..74175429 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72608514-74386749)x1 copy number loss not provided [RCV000682892] Chr7:72608514..74386749 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72701018-74143240)x3 copy number gain not provided [RCV000682886] Chr7:72701018..74143240 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72577021-74147166)x3 copy number gain not provided [RCV000682887] Chr7:72577021..74147166 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72589515-74386749)x1 copy number loss not provided [RCV000682894] Chr7:72589515..74386749 [GRCh37]
Chr7:7q11.23
pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Speech-language disorder 1 [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7q11.23(chr7:72305671-74196360)x1 copy number loss not provided [RCV000746789] Chr7:72305671..74196360 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:73023062-73524207)x1 copy number loss not provided [RCV000746796] Chr7:73023062..73524207 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72650106-74138603)x1 copy number loss not provided [RCV000746790] Chr7:72650106..74138603 [GRCh37]
Chr7:7q11.23
pathogenic
Single allele duplication Schizophrenia [RCV000754333] Chr7:73312644..74726596 [GRCh38]
Chr7:7q11.23
pathogenic
Single allele duplication Autistic disorder of childhood onset [RCV000754334] Chr7:73323103..74726596 [GRCh38]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72719386-74218536)x1 copy number loss not provided [RCV000746793] Chr7:72719386..74218536 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72650265-74138603)x1 copy number loss not provided [RCV000746791] Chr7:72650265..74138603 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72653306-74134911)x1 copy number loss not provided [RCV000746792] Chr7:72653306..74134911 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72722981-74200092)x1 copy number loss not provided [RCV000746794] Chr7:72722981..74200092 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72743983-74145064)x3 copy number gain not provided [RCV000746795] Chr7:72743983..74145064 [GRCh37]
Chr7:7q11.23
pathogenic
Single allele duplication Congenital malrotation of intestine [RCV000754986] Chr7:72634873..74142327 [GRCh37]
Chr7:7q11.23
likely pathogenic
NM_032951.3(MLXIPL):c.375C>T (p.Ala125=) single nucleotide variant not provided [RCV000927387] Chr7:73616096 [GRCh38]
Chr7:73030426 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1095C>A (p.Pro365=) single nucleotide variant not provided [RCV000947020] Chr7:73597690 [GRCh38]
Chr7:73012020 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.2428G>A (p.Ala810Thr) single nucleotide variant not provided [RCV000900416] Chr7:73594286 [GRCh38]
Chr7:73008616 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.620C>T (p.Ala207Val) single nucleotide variant not provided [RCV000883826] Chr7:73606110 [GRCh38]
Chr7:73020440 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1554C>G (p.Pro518=) single nucleotide variant not provided [RCV000879162] Chr7:73597231 [GRCh38]
Chr7:73011561 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.732C>A (p.Asp244Glu) single nucleotide variant not provided [RCV000947021] Chr7:73605998 [GRCh38]
Chr7:73020328 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.2059-8G>A single nucleotide variant not provided [RCV000922191] Chr7:73595977 [GRCh38]
Chr7:73010307 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.573+7G>A single nucleotide variant not provided [RCV000950159] Chr7:73607324 [GRCh38]
Chr7:73021654 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1096T>C (p.Leu366=) single nucleotide variant not provided [RCV000880477] Chr7:73597689 [GRCh38]
Chr7:73012019 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.874A>C (p.Ser292Arg) single nucleotide variant not provided [RCV000880478] Chr7:73605715 [GRCh38]
Chr7:73020045 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.2272G>A (p.Val758Ile) single nucleotide variant not provided [RCV000972155] Chr7:73595675 [GRCh38]
Chr7:73010005 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1537G>A (p.Ala513Thr) single nucleotide variant not provided [RCV000967051] Chr7:73597248 [GRCh38]
Chr7:73011578 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1198C>G (p.Pro400Ala) single nucleotide variant not provided [RCV000967052] Chr7:73597587 [GRCh38]
Chr7:73011917 [GRCh37]
Chr7:7q11.23
benign
Single allele deletion not provided [RCV000768460] Chr7:72682338..74141250 [GRCh37]
Chr7:7q11.23
likely pathogenic
GRCh37/hg19 7q11.23(chr7:72700996-74142190) copy number loss Williams syndrome [RCV000767639] Chr7:72700996..74142190 [GRCh37]
Chr7:7q11.23
pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787465] Chr7:72699382..74142329 [GRCh37]
Chr7:7q11.23
pathogenic
NM_032951.3(MLXIPL):c.2490C>T (p.Thr830=) single nucleotide variant not provided [RCV000952538] Chr7:73593934 [GRCh38]
Chr7:73008264 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.444C>G (p.Pro148=) single nucleotide variant not provided [RCV000894233] Chr7:73607629 [GRCh38]
Chr7:73021959 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.22C>T (p.Leu8=) single nucleotide variant not provided [RCV000925666] Chr7:73624471 [GRCh38]
Chr7:73038801 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.791C>A (p.Pro264His) single nucleotide variant not provided [RCV000923189] Chr7:73605939 [GRCh38]
Chr7:73020269 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.795G>A (p.Ser265=) single nucleotide variant not provided [RCV000968847] Chr7:73605935 [GRCh38]
Chr7:73020265 [GRCh37]
Chr7:7q11.23
likely benign
GRCh37/hg19 7q11.23(chr7:72744494-74339044) copy number loss Williams syndrome [RCV000767637] Chr7:72744494..74339044 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72744494-76038818) copy number loss Williams syndrome [RCV000767638] Chr7:72744494..76038818 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72772522-74133319) copy number loss Williams syndrome [RCV000767640] Chr7:72772522..74133319 [GRCh37]
Chr7:7q11.23
pathogenic
NM_032951.3(MLXIPL):c.2124G>A (p.Ala708=) single nucleotide variant not provided [RCV000958340] Chr7:73595904 [GRCh38]
Chr7:73010234 [GRCh37]
Chr7:7q11.23
benign
Single allele duplication Neurodevelopmental disorder [RCV000787457] Chr7:72364526..73780265 [GRCh37]
Chr7:7q11.23
likely pathogenic
NM_032951.3(MLXIPL):c.1899G>A (p.Pro633=) single nucleotide variant not provided [RCV000940450] Chr7:73596403 [GRCh38]
Chr7:73010733 [GRCh37]
Chr7:7q11.23
likely benign
Single allele deletion Neurodevelopmental disorder [RCV000787466] Chr7:72726590..74142329 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72996564-73597315)x1 copy number loss not provided [RCV001005968] Chr7:72996564..73597315 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72722981-74141840)x3 copy number gain See cases [RCV001194543] Chr7:72722981..74141840 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72621722-76007380)x1 copy number loss not provided [RCV001005967] Chr7:72621722..76007380 [GRCh37]
Chr7:7q11.23
pathogenic
NM_032951.3(MLXIPL):c.210G>A (p.Gly70=) single nucleotide variant not provided [RCV000927240] Chr7:73624283 [GRCh38]
Chr7:73038613 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.594A>G (p.Glu198=) single nucleotide variant not provided [RCV000905092] Chr7:73606998 [GRCh38]
Chr7:73021328 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.483+8G>A single nucleotide variant not provided [RCV000963451] Chr7:73607582 [GRCh38]
Chr7:73021912 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1563G>A (p.Ala521=) single nucleotide variant not provided [RCV000974084] Chr7:73597222 [GRCh38]
Chr7:73011552 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1514C>T (p.Ala505Val) single nucleotide variant not provided [RCV000938576] Chr7:73597271 [GRCh38]
Chr7:73011601 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1971G>A (p.Ala657=) single nucleotide variant not provided [RCV000941505] Chr7:73596240 [GRCh38]
Chr7:73010570 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.2167G>A (p.Glu723Lys) single nucleotide variant not provided [RCV000880027] Chr7:73595861 [GRCh38]
Chr7:73010191 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1428C>T (p.Pro476=) single nucleotide variant not provided [RCV000970784] Chr7:73597357 [GRCh38]
Chr7:73011687 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1467C>A (p.Ser489=) single nucleotide variant not provided [RCV000954032] Chr7:73597318 [GRCh38]
Chr7:73011648 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.486C>G (p.Ala162=) single nucleotide variant not provided [RCV000932867] Chr7:73607418 [GRCh38]
Chr7:73021748 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.2181C>T (p.Ala727=) single nucleotide variant not provided [RCV000939514] Chr7:73595847 [GRCh38]
Chr7:73010177 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1206C>G (p.Ala402=) single nucleotide variant not provided [RCV000931374] Chr7:73597579 [GRCh38]
Chr7:73011909 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.861G>A (p.Thr287=) single nucleotide variant not provided [RCV000932926] Chr7:73605728 [GRCh38]
Chr7:73020058 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.2521C>T (p.Arg841Trp) single nucleotide variant not provided [RCV000954107] Chr7:73593903 [GRCh38]
Chr7:73008233 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1715C>A (p.Thr572Asn) single nucleotide variant not provided [RCV000943352] Chr7:73596746 [GRCh38]
Chr7:73011076 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1483C>T (p.Pro495Ser) single nucleotide variant not provided [RCV000973572] Chr7:73597302 [GRCh38]
Chr7:73011632 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1968C>T (p.Ser656=) single nucleotide variant not provided [RCV000933458] Chr7:73596243 [GRCh38]
Chr7:73010573 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.618+7G>A single nucleotide variant not provided [RCV000911957] Chr7:73606967 [GRCh38]
Chr7:73021297 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.1813G>T (p.Ala605Ser) single nucleotide variant not provided [RCV000933638] Chr7:73596648 [GRCh38]
Chr7:73010978 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.573+8G>C single nucleotide variant not provided [RCV000913654] Chr7:73607323 [GRCh38]
Chr7:73021653 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1251C>G (p.Pro417=) single nucleotide variant not provided [RCV000911481] Chr7:73597534 [GRCh38]
Chr7:73011864 [GRCh37]
Chr7:7q11.23
likely benign
NM_032951.3(MLXIPL):c.293+6G>A single nucleotide variant not provided [RCV000890272] Chr7:73624194 [GRCh38]
Chr7:73038524 [GRCh37]
Chr7:7q11.23
benign
NM_032951.3(MLXIPL):c.1671+10C>T single nucleotide variant not provided [RCV000935006] Chr7:73596855 [GRCh38]
Chr7:73011185 [GRCh37]
Chr7:7q11.23
benign
Single allele deletion Williams syndrome [RCV001172267] Chr7:72657228..74160300 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72403117-76709600)x1 copy number loss not provided [RCV001258798] Chr7:72403117..76709600 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.22-11.23(chr7:68977230-73939510)x1 copy number loss not provided [RCV001260005] Chr7:68977230..73939510 [GRCh37]
Chr7:7q11.22-11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72659674-74164894)x3 copy number gain not provided [RCV001258797] Chr7:72659674..74164894 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:73019031-73040891)x1 copy number loss not provided [RCV001258800] Chr7:73019031..73040891 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.22-11.23(chr7:71847968-73391310) copy number loss Williams syndrome [RCV001352633] Chr7:71847968..73391310 [GRCh37]
Chr7:7q11.22-11.23
likely pathogenic
GRCh37/hg19 7q11.23(chr7:72717369-74142224)x1 copy number loss not provided [RCV001270666] Chr7:72717369..74142224 [GRCh37]
Chr7:7q11.23
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12744 AgrOrtholog
COSMIC MLXIPL COSMIC
Ensembl Genes ENSG00000009950 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000320886 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000343767 UniProtKB/Swiss-Prot
  ENSP00000346629 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000392636 UniProtKB/TrEMBL
  ENSP00000395172 UniProtKB/TrEMBL
  ENSP00000402615 UniProtKB/TrEMBL
  ENSP00000406296 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000412330 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000313375 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000345114 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000354613 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000414749 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000429400 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000434326 UniProtKB/TrEMBL
  ENST00000453275 UniProtKB/TrEMBL
  ENST00000456640 UniProtKB/TrEMBL
Gene3D-CATH 4.10.280.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000009950 GTEx
HGNC ID HGNC:12744 ENTREZGENE
Human Proteome Map MLXIPL Human Proteome Map
InterPro bHLH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HLH_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:51085 UniProtKB/Swiss-Prot
NCBI Gene 51085 ENTREZGENE
OMIM 605678 OMIM
Pfam HLH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37353 PharmGKB
PROSITE BHLH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HLH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47459 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0C4DG26_HUMAN UniProtKB/TrEMBL
  C5HU01_HUMAN UniProtKB/TrEMBL
  C9JDF5_HUMAN UniProtKB/TrEMBL
  H7C1V3_HUMAN UniProtKB/TrEMBL
  MLXPL_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  S5LSP3_HUMAN UniProtKB/TrEMBL
  S5LVX6_HUMAN UniProtKB/TrEMBL
  S5M7A5_HUMAN UniProtKB/TrEMBL
UniProt Secondary C5HU02 UniProtKB/Swiss-Prot
  C5HU03 UniProtKB/Swiss-Prot
  C5HU04 UniProtKB/Swiss-Prot
  Q96E48 UniProtKB/Swiss-Prot
  Q9BY03 UniProtKB/Swiss-Prot
  Q9BY04 UniProtKB/Swiss-Prot
  Q9BY05 UniProtKB/Swiss-Prot
  Q9BY06 UniProtKB/Swiss-Prot
  Q9Y2P3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-21 MLXIPL  MLX interacting protein like  MLXIPL  MLX interacting protein-like  Symbol and/or name change 5135510 APPROVED