NRG1 (neuregulin 1) - Rat Genome Database

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Gene: NRG1 (neuregulin 1) Homo sapiens
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Symbol: NRG1
Name: neuregulin 1
RGD ID: 731515
HGNC Page HGNC:7997
Description: Enables protein tyrosine kinase activator activity; signaling receptor binding activity; and transcription coregulator activity. Involved in several processes, including ERBB signaling pathway; heart development; and negative regulation of apoptotic process. Acts upstream of or within negative regulation of DNA-templated transcription. Located in apical plasma membrane and nucleoplasm. Is active in extracellular space and glutamatergic synapse. Implicated in several diseases, including bipolar disorder; cerebral malaria; dementia; middle cerebral artery infarction; and psychotic disorder (multiple). Biomarker of Alzheimer's disease; hepatocellular carcinoma; major depressive disorder; and ovarian cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: acetylcholine receptor-inducing activity; ARIA; GGF; GGF2; glial growth factor; glial growth factor 2; heregulin, alpha (45kD, ERBB2 p185-activator); HGL; HRG; HRG1; HRGA; MST131; MSTP131; NDF; neu differentiation factor; neuregulin 1 type IV beta 1a; neuregulin 1 type IV beta 3; NRG1 class VII isoform alpha 2a; NRG1 class VII isoform alpha 2b; NRG1 class VII isoform alpha beta 2a; NRG1 class VII isoform alpha beta 3; NRG1 class VII isoform beta 2a; NRG1 class VII isoform beta 3; NRG1 intronic transcript 2 (non-protein coding); NRG1-IT2; pro-neuregulin-1, membrane-bound isoform; pro-NRG1; sensory and motor neuron derived factor; SMDF
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
GRCh38831,639,245 - 32,774,046 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl831,639,222 - 32,855,666 (+)EnsemblGRCh38hg38GRCh38
GRCh37831,496,761 - 32,631,564 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36831,616,810 - 32,741,615 (+)NCBINCBI36Build 36hg18NCBI36
Build 34832,525,654 - 32,741,615NCBI
Celera830,430,833 - 31,581,276 (+)NCBICelera
Cytogenetic Map8p12NCBI
HuRef830,042,037 - 31,167,972 (+)NCBIHuRef
CHM1_1831,698,276 - 32,824,231 (+)NCBICHM1_1
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
alcohol use disorder  (IAGP)
Alzheimer's disease  (IEP)
amblyopia  (ISO)
amphetamine abuse  (EXP)
amyotrophic lateral sclerosis  (IMP)
bipolar disorder  (IAGP)
Breast Neoplasms  (EXP)
cannabis abuse  (IEP)
cannabis dependence  (IAGP)
Cardiotoxicity  (EXP)
cerebral malaria  (IDA,ISO)
Charcot-Marie-Tooth disease  (IDA)
congestive heart failure  (EXP)
contact dermatitis  (EXP)
COVID-19  (HEP)
dementia  (IDA)
Diabetic Cardiomyopathies  (ISO)
diabetic neuropathy  (ISO)
epilepsy  (ISO)
Experimental Liver Cirrhosis  (EXP)
Febrile Seizures  (HEP)
gastric ulcer  (EXP)
genetic disease  (IAGP)
hepatocellular carcinoma  (IEP)
hereditary spastic paraplegia  (IAGP)
Hirschsprung's disease  (EXP)
Hyperalgesia  (ISO)
influenza  (ISO)
interstitial cystitis  (ISO)
juvenile rheumatoid arthritis  (EXP)
Lung Neoplasms  (EXP)
major depressive disorder  (IEP)
median neuropathy  (ISO)
middle cerebral artery infarction  (IDA)
movement disease  (EXP)
myocardial infarction  (IDA)
Neointima  (ISO)
Neoplasm Invasiveness  (EXP)
Neoplastic Cell Transformation  (EXP)
Nerve Degeneration  (ISO)
obstructive sleep apnea  (IAGP)
ovarian cancer  (IEP)
overactive bladder syndrome  (ISO)
Pain  (EXP)
polycystic ovary syndrome  (EXP)
psychotic disorder  (IAGP)
schizophrenia  (EXP,ISO,ISS)
schizophrenia 6  (IAGP)
sciatic neuropathy  (ISO)
skin papilloma  (HEP)
Spinal Cord Injuries  (ISO)
stress-related disorder  (ISO)
Subarachnoid Hemorrhage  (IEP)
substance abuse  (IAGP)
Tobacco Use Disorder  (IAGP)
transient cerebral ischemia  (IMP)
tuberculosis  (IAGP)
Viral Myocarditis  (ISO)
visual epilepsy  (ISO)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
1-benzylpiperazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
1-nitropyrene  (EXP)
17beta-estradiol  (EXP,ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (EXP,ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4,6-trinitrotoluene  (ISO)
2,4-D  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
2-nitrofluorene  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-\{1-[3-(dimethylamino)propyl]-1H-indol-3-yl\}-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione  (EXP)
3-chloropropane-1,2-diol  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-(N-nitrosomethylamino)-1-(3-pyridyl)butan-1-one  (ISO)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
AACOCF3  (EXP)
acetamide  (ISO)
acrylamide  (EXP)
aflatoxin B1  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
aldehydo-D-glucose  (ISO)
all-trans-retinoic acid  (EXP)
aluminium atom  (EXP)
aluminium(0)  (EXP)
amiodarone  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
androgen antagonist  (ISO)
antimycin A  (EXP)
aristolochic acid A  (EXP)
Aroclor 1254  (ISO)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
arsenite(3-)  (EXP)
arsenous acid  (EXP,ISO)
azoxystrobin  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
beta-naphthoflavone  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP,ISO)
butan-1-ol  (EXP)
butanal  (EXP)
Butylparaben  (EXP,ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP,ISO)
cannabidiol  (EXP)
carbofuran  (ISO)
carbon nanotube  (ISO)
celecoxib  (EXP)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
choline  (ISO)
clozapine  (EXP,ISO)
cobalt dichloride  (EXP)
colforsin daropate hydrochloride  (ISO)
copper(II) sulfate  (EXP)
coumarin  (EXP)
crocidolite asbestos  (EXP,ISO)
cyclophosphamide  (EXP)
cyclosporin A  (EXP)
D-glucose  (ISO)
DDE  (ISO)
decabromodiphenyl ether  (ISO)
dexamethasone  (ISO)
diarsenic trioxide  (EXP,ISO)
dibutyl phthalate  (ISO)
diethylstilbestrol  (ISO)
dimethylarsinic acid  (EXP)
dimethylarsinous acid  (EXP)
dioxygen  (ISO)
diquat  (ISO)
disodium selenite  (ISO)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
entinostat  (EXP)
enzacamene  (ISO)
epoxiconazole  (ISO)
etoposide  (EXP)
fenamidone  (ISO)
fenvalerate  (ISO)
fluoranthene  (ISO)
flutamide  (ISO)
folic acid  (ISO)
fonofos  (EXP)
fructose  (ISO)
fulvestrant  (EXP)
furan  (ISO)
gemcitabine  (EXP)
gentamycin  (ISO)
glucose  (ISO)
haloperidol  (ISO)
Heliotrine  (ISO)
hydrogen peroxide  (ISO)
indole-3-methanol  (ISO)
ketamine  (ISO)
L-methionine  (ISO)
linuron  (ISO)
lipopolysaccharide  (EXP)
LY294002  (EXP,ISO)
maneb  (ISO)
manganese(II) chloride  (ISO)
methamphetamine  (EXP)
methapyrilene  (EXP,ISO)
methimazole  (ISO)
methotrexate  (EXP)
methoxychlor  (ISO)
methyl methanesulfonate  (EXP)
methylmercury chloride  (EXP)
mifepristone  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
N,N-diethyl-m-toluamide  (ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
N-methyl-4-phenylpyridinium  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
N-nitrosomorpholine  (ISO)
N-tosyl-L-phenylalanyl chloromethyl ketone  (ISO)
naphthalene  (ISO)
nickel atom  (EXP)
nickel dichloride  (EXP)
nickel sulfate  (EXP)
ochratoxin A  (EXP)
orphenadrine  (ISO)
oxaliplatin  (ISO)
ozone  (ISO)
panobinostat  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
parathion  (EXP)
PCB138  (EXP)
pentane-2,3-dione  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP,ISO)
permethrin  (ISO)
phenobarbital  (EXP)
phenylephrine  (ISO)
phenylmercury acetate  (EXP)
phorbol 13-acetate 12-myristate  (ISO)
picoxystrobin  (EXP)
piperonyl butoxide  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
potassium dichromate  (ISO)
prochloraz  (ISO)
procymidone  (ISO)
progesterone  (ISO)
propanal  (EXP)
propiconazole  (ISO)
propylparaben  (EXP)
prostaglandin E2  (EXP)
Ptaquiloside  (ISO)
pyrimidifen  (EXP)
raloxifene  (EXP)
resveratrol  (EXP)
risperidone  (ISO)
rotenone  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
senecionine  (ISO)
serpentine asbestos  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
sodium dichromate  (ISO)
Soman  (ISO)
sulfadimethoxine  (ISO)
sulforaphane  (EXP)
sunitinib  (EXP)
tamoxifen  (EXP)
tebufenpyrad  (EXP)
temozolomide  (EXP)
tephrosin  (EXP)
terbufos  (EXP)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
Theaflavin 3,3'-digallate  (EXP)
thioacetamide  (ISO)
topotecan  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triphenyl phosphate  (ISO)
triptonide  (ISO)
troglitazone  (EXP)
tyrphostin AG 1478  (ISO)
valproic acid  (EXP)
vinclozolin  (ISO)
vorinostat  (EXP)
zinc sulfate  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
animal organ development  (IBA,IEA)
cardiac conduction system development  (ISO)
cardiac muscle cell differentiation  (ISS)
cardiac muscle cell myoblast differentiation  (IDA)
cardiac muscle tissue development  (ISO)
cell communication  (TAS)
cell differentiation  (IBA,IEA)
cell morphogenesis  (ISO)
cell population proliferation  (IDA)
cell surface receptor protein tyrosine kinase signaling pathway  (IDA)
cellular response to acetylcholine  (ISO)
cellular response to L-glutamate  (ISO)
cellular response to mechanical stimulus  (ISO)
cellular response to serotonin  (ISO)
chemorepulsion involved in interneuron migration from the subpallium to the cortex  (ISO)
detection of temperature stimulus involved in sensory perception of pain  (ISO)
endocardial cell differentiation  (IDA)
ERBB signaling pathway  (IDA,IMP)
ERBB2-ERBB3 signaling pathway  (IDA)
ERBB2-ERBB4 signaling pathway  (IDA)
ERBB3 signaling pathway  (IDA)
ERBB4 signaling pathway  (IDA)
ERBB4-ERBB4 signaling pathway  (IDA)
glial cell differentiation  (ISO)
glial cell fate commitment  (ISO)
heart development  (ISO)
intracellular signal transduction  (IBA,IEA)
locomotory behavior  (ISO)
mammary gland development  (TAS)
MAPK cascade  (ISO)
memory  (ISO)
muscle organ development  (ISO)
myelination  (ISO)
myelination in peripheral nervous system  (ISO)
negative chemotaxis  (IEA)
negative regulation of cardiac muscle cell apoptotic process  (IDA)
negative regulation of corticosterone secretion  (ISO)
negative regulation of DNA-templated transcription  (IDA)
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand  (IDA)
negative regulation of neuron migration  (ISO)
negative regulation of protein catabolic process  (ISO)
negative regulation of secretion  (IDA)
nervous system development  (IBA,IEA,ISO,TAS)
neural crest cell development  (TAS)
neuron fate commitment  (ISO)
neuron migration  (ISO)
oligodendrocyte differentiation  (ISO)
peripheral nervous system development  (ISO)
phosphatidylinositol 3-kinase/protein kinase B signal transduction  (ISO)
positive regulation of axon regeneration  (ISO)
positive regulation of calcineurin-NFAT signaling cascade  (ISO)
positive regulation of cardiac muscle cell differentiation  (ISO)
positive regulation of cardiac muscle cell proliferation  (IDA)
positive regulation of cell adhesion  (IDA)
positive regulation of cell growth  (IDA)
positive regulation of cell population proliferation  (IMP,ISO)
positive regulation of ERK1 and ERK2 cascade  (IMP)
positive regulation of gene expression  (ISO)
positive regulation of membrane permeability  (ISO)
positive regulation of neural precursor cell proliferation  (ISO)
positive regulation of neuron projection development  (ISO)
positive regulation of peptidyl-tyrosine autophosphorylation  (IDA)
positive regulation of peptidyl-tyrosine phosphorylation  (ISO)
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction  (ISO)
positive regulation of protein-containing complex assembly  (IDA,TAS)
positive regulation of Ras protein signal transduction  (ISO)
positive regulation of Schwann cell proliferation  (ISO)
positive regulation of striated muscle cell differentiation  (ISS)
postsynapse to nucleus signaling pathway  (ISO)
protein catabolic process  (ISO)
regulation of cell differentiation  (ISO)
regulation of postsynaptic neurotransmitter receptor internalization  (IDA,IMP)
regulation of presynapse assembly  (ISO)
response to muscle activity  (ISO)
response to nutrient levels  (ISO)
response to progesterone  (ISO)
response to vitamin D  (ISO)
Schwann cell development  (ISO)
Schwann cell differentiation  (ISO)
sensory perception of pain  (ISO)
sequestering of metal ion  (EXP)
signal transduction  (IEA)
synapse assembly  (ISO)
synaptic membrane adhesion  (ISO)
ventricular cardiac muscle cell differentiation  (IDA)
ventricular trabecula myocardium morphogenesis  (IDA)
wound healing  (IDA,TAS)

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

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Genome-Wide Tiling Array Analysis of HPV-Induced Warts Reveals Aberrant Methylation of Protein-Coding and Non-Coding Regions. Al-Eitan LN, etal., Genes (Basel). 2019 Dec 27;11(1). pii: genes11010034. doi: 10.3390/genes11010034.
2. Neonatal infection with neurotropic influenza A virus affects working memory and expression of type III Nrg1 in adult mice. Asp L, etal., Brain Behav Immun. 2009 Aug;23(6):733-41. doi: 10.1016/j.bbi.2009.04.004. Epub 2009 Apr 10.
3. Neuregulin-1 is increased in schizophrenia patients with chronic cannabis abuse: Preliminary results. Aukst Margetic B, etal., Schizophr Res. 2019 Jun;208:473-474. doi: 10.1016/j.schres.2019.02.007. Epub 2019 Feb 22.
4. Associations of Sleep Apnea, NRG1 Polymorphisms, Alcohol Consumption, and Cerebral White Matter Hyperintensities: Analysis with Genome-Wide Association Data. Baik I, etal., Sleep. 2015 Jul 1;38(7):1137-43. doi: 10.5665/sleep.4830.
5. Neuregulin-1 controls an endogenous repair mechanism after spinal cord injury. Bartus K, etal., Brain. 2016 Mar 17. pii: aww039.
6. Heregulin-1ß and HER3 in hepatocellular carcinoma: status and regulation by insulin. Buta C, etal., J Exp Clin Cancer Res. 2016 Aug 11;35(1):126. doi: 10.1186/s13046-016-0402-3.
7. Neuregulin-1 and erbB4 immunoreactivity is associated with neuritic plaques in Alzheimer disease brain and in a transgenic model of Alzheimer disease. Chaudhury AR, etal., J Neuropathol Exp Neurol. 2003 Jan;62(1):42-54.
8. Neuregulin-1-ErbB signaling promotes microglia activation contributing to mechanical allodynia of cyclophosphamide-induced cystitis. Chen JL, etal., Neurourol Urodyn. 2019 Jun;38(5):1250-1260. doi: 10.1002/nau.24005. Epub 2019 Apr 15.
9. Interfering effect and mechanism of neuregulin on experimental dementia model in rats. Chen Y, etal., Behav Brain Res. 2011 Sep 23;222(2):321-5. doi: 10.1016/j.bbr.2011.03.063. Epub 2011 Apr 5.
10. Neuregulin-1 attenuates neointimal formation following vascular injury and inhibits the proliferation of vascular smooth muscle cells. Clement CM, etal., J Vasc Res. 2007;44(4):303-12. Epub 2007 Apr 16.
11. Investigating the Role of Gene-Gene Interactions in TB Susceptibility. Daya M, etal., PLoS One. 2015 Apr 28;10(4):e0123970. doi: 10.1371/journal.pone.0123970. eCollection 2014.
12. Expressions of neuregulin 1beta and ErbB4 in prefrontal cortex and hippocampus of a rat schizophrenia model induced by chronic MK-801 administration. Feng Y, etal., J Biomed Biotechnol. 2010;2010:859516. doi: 10.1155/2010/859516. Epub 2010 May 4.
13. Soluble neuregulin-1 modulates disease pathogenesis in rodent models of Charcot-Marie-Tooth disease 1A. Fledrich R, etal., Nat Med. 2014 Sep;20(9):1055-61. doi: 10.1038/nm.3664. Epub 2014 Aug 24.
14. Controlled delivery of fibroblast growth factor-1 and neuregulin-1 from biodegradable microparticles promotes cardiac repair in a rat myocardial infarction model through activation of endogenous regeneration. Formiga FR, etal., J Control Release. 2014 Jan 10;173:132-9. doi: 10.1016/j.jconrel.2013.10.034. Epub 2013 Nov 5.
15. Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses. Go RC, etal., Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):28-32.
16. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
17. Cation-independent mannose 6-phosphate and 78 kDa receptors for lysosomal enzyme targeting are located in different cell compartments. Gonzalez-Noriega A, etal., Biochim Biophys Acta. 2005 Aug 15;1745(1):7-19. Epub 2005 Jan 26.
18. Neuregulin-1/ErbB signaling is impaired in the rat model of diabetic cardiomyopathy. Gui C, etal., Cardiovasc Pathol. 2012 Sep-Oct;21(5):414-20. doi: 10.1016/j.carpath.2011.12.006. Epub 2012 Jan 28.
19. Linkage analysis followed by association show NRG1 associated with cannabis dependence in African Americans. Han S, etal., Biol Psychiatry. 2012 Oct 15;72(8):637-44. doi: 10.1016/j.biopsych.2012.02.038. Epub 2012 Apr 19.
20. Cleavage and Sub-Cellular Redistribution of Nuclear Pore Protein 98 by Coxsackievirus B3 Protease 2A Impairs Cardioprotection. Hanson PJ, etal., Front Cell Infect Microbiol. 2019 Jul 24;9:265. doi: 10.3389/fcimb.2019.00265. eCollection 2019.
21. Glial growth factor 2 promotes functional recovery with treatment initiated up to 7 days after permanent focal ischemic stroke. Iaci JF, etal., Neuropharmacology. 2010 Dec;59(7-8):640-9. doi: 10.1016/j.neuropharm.2010.07.017. Epub 2010 Aug 4.
22. Glutamate-dependent ectodomain shedding of neuregulin-1 type II precursors in rat forebrain neurons. Iwakura Y, etal., PLoS One. 2017 Mar 28;12(3):e0174780. doi: 10.1371/journal.pone.0174780. eCollection 2017.
23. Changes of neuregulin-1 (NRG-1) expression in a rat model of overactive bladder induced by partial urethral obstruction: is NRG-1 a new biomarker of overactive bladder? Jang H, etal., BMC Urol. 2013 Oct 23;13:54. doi: 10.1186/1471-2490-13-54.
24. The Stress-Induced Transcription Factor NR4A1 Adjusts Mitochondrial Function and Synapse Number in Prefrontal Cortex. Jeanneteau F, etal., J Neurosci. 2018 Feb 7;38(6):1335-1350. doi: 10.1523/JNEUROSCI.2793-17.2017. Epub 2018 Jan 2.
25. Secretion of EGF-like domain of heregulinbeta promotes axonal growth and functional recovery of injured sciatic nerve. Joung I, etal., Mol Cells. 2010 Nov;30(5):477-84. doi: 10.1007/s10059-010-0137-5. Epub 2010 Oct 14.
26. Expression changes of the neuregulin 1 isoforms in neuropathic pain model rats. Kanzaki H, etal., Neurosci Lett. 2012 Feb 6;508(2):78-83. doi: 10.1016/j.neulet.2011.12.023. Epub 2011 Dec 28.
27. Analysis of gene-expression profiles by oligonucleotide microarray in children with influenza. Kawada J, etal., J Gen Virol. 2006 Jun;87(Pt 6):1677-83. doi: 10.1099/vir.0.81670-0.
28. Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population. Kim JW, etal., 2006 Apr 5;141B(3):281-6. doi: 10.1002/ajmg.b.30209.
29. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families. Liu CM, etal., Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):79-83. doi: 10.1002/ajmg.b.20161.
30. Randomized Phase II Trial of Seribantumab in Combination With Paclitaxel in Patients With Advanced Platinum-Resistant or -Refractory Ovarian Cancer. Liu JF, etal., J Clin Oncol. 2016 Dec 20;34(36):4345-4353. doi: 10.1200/JCO.2016.67.1891. Epub 2016 Oct 23.
31. Neuregulin-1 attenuates experimental cerebral malaria (ECM) pathogenesis by regulating ErbB4/AKT/STAT3 signaling. Liu M, etal., J Neuroinflammation. 2018 Apr 10;15(1):104. doi: 10.1186/s12974-018-1147-z.
32. The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder. Mechelli A, etal., Neuroimage. 2008 Aug 15;42(2):817-26. doi: 10.1016/j.neuroimage.2008.05.025. Epub 2008 May 27.
33. No association between neuregulin 1 and psychotic symptoms in Alzheimer's disease patients. Middle F, etal., J Alzheimers Dis. 2010;20(2):561-7. doi: 10.3233/JAD-2010-1405.
34. Neuregulins and cancer. Montero JC, etal., Clin Cancer Res. 2008 Jun 1;14(11):3237-41. doi: 10.1158/1078-0432.CCR-07-5133.
35. Gene therapy for overexpressing Neuregulin 1 type I in skeletal muscles promotes functional improvement in the SOD1G93A ALS mice. Mòdol-Caballero G, etal., Neurobiol Dis. 2020 Apr;137:104793. doi: 10.1016/j.nbd.2020.104793. Epub 2020 Feb 4.
36. Denervation and reinnervation of adult skeletal muscle modulate mRNA expression of neuregulin-1 and ErbB receptors. Nicolino S, etal., Microsurgery. 2009;29(6):464-72. doi: 10.1002/micr.20636.
37. Overexpression of Neuregulin 1 Type III Confers Hippocampal mRNA Alterations and Schizophrenia-Like Behaviors in Mice. Olaya JC, etal., Schizophr Bull. 2018 Jun 6;44(4):865-875. doi: 10.1093/schbul/sbx122.
38. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
39. Expression of heregulin in human coronary atherosclerotic lesions. Panutsopulos D, etal., J Vasc Res. 2005 Nov-Dec;42(6):463-74. Epub 2005 Sep 6.
40. Effects of neuregulin GGF2 (cimaglermin alfa) dose and treatment frequency on left ventricular function in rats following myocardial infarction. Parry TJ, etal., Eur J Pharmacol. 2017 Feb 5;796:76-89. doi: 10.1016/j.ejphar.2016.12.024. Epub 2016 Dec 16.
41. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
42. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
43. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
44. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
45. Irreversible changes occurring in long-term denervated Schwann cells affect delayed nerve repair. Ronchi G, etal., J Neurosurg. 2017 Oct;127(4):843-856. doi: 10.3171/2016.9.JNS16140. Epub 2017 Jan 6.
46. Therapeutic efficacy of neuregulin 1-expressing human adipose-derived mesenchymal stem cells for ischemic stroke. Ryu S, etal., PLoS One. 2019 Sep 27;14(9):e0222587. doi: 10.1371/journal.pone.0222587. eCollection 2019.
47. Neuregulin-1 attenuates mortality associated with experimental cerebral malaria. Solomon W, etal., J Neuroinflammation. 2014 Jan 17;11:9. doi: 10.1186/1742-2094-11-9.
48. Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons. Tan GH, etal., Nat Neurosci. 2011 Dec 11;15(2):258-66. doi: 10.1038/nn.3005.
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50. A functional neuregulin-1 gene variant and stressful life events: Effect on drug use in a longitudinal population-representative cohort study. Vaht M, etal., J Psychopharmacol. 2017 Jan;31(1):54-61. doi: 10.1177/0269881116655979. Epub 2016 Jul 10.
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52. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
53. Effect of regulation of the NRG1/ErbB4 signaling pathway on the visual cortex synaptic plasticity of amblyopic adult rats. Xu L, etal., J Biochem Mol Toxicol. 2021 Sep;35(9):e22841. doi: 10.1002/jbt.22841. Epub 2021 Jul 17.
54. ErbB4 protects against neuronal apoptosis via activation of YAP/PIK3CB signaling pathway in a rat model of subarachnoid hemorrhage. Yan F, etal., Exp Neurol. 2017 Nov;297:92-100. doi: 10.1016/j.expneurol.2017.07.014. Epub 2017 Jul 27.
55. Traditional chinese medicine tang-luo-ning ameliorates sciatic nerve injuries in streptozotocin-induced diabetic rats. Zou DW, etal., Evid Based Complement Alternat Med. 2013;2013:989670. doi: 10.1155/2013/989670. Epub 2013 Oct 28.
Additional References at PubMed
PMID:1348215   PMID:1350381   PMID:7509448   PMID:7514177   PMID:7556068   PMID:7592681   PMID:7689552   PMID:7721889   PMID:7730382   PMID:7782315   PMID:7876250   PMID:7903175  
PMID:8062828   PMID:8095334   PMID:8096067   PMID:8125298   PMID:8325659   PMID:8702572   PMID:8702723   PMID:9168114   PMID:9168115   PMID:9333014   PMID:9342050   PMID:9553078  
PMID:9565587   PMID:9685409   PMID:10372964   PMID:10523851   PMID:10537356   PMID:10559227   PMID:10585499   PMID:10597312   PMID:10913256   PMID:11042203   PMID:11116142   PMID:11389077  
PMID:11555649   PMID:11896060   PMID:12082616   PMID:12145742   PMID:12204892   PMID:12471041   PMID:12477932   PMID:12478479   PMID:12509456   PMID:12556556   PMID:12600989   PMID:12646923  
PMID:12768307   PMID:12800145   PMID:12808428   PMID:12874607   PMID:14569272   PMID:14632199   PMID:14647391   PMID:14699424   PMID:14702039   PMID:14729827   PMID:14966480   PMID:15007393  
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PMID:17447867   PMID:17499242   PMID:17503451   PMID:17519028   PMID:17562386   PMID:17565985   PMID:17598910   PMID:17602072   PMID:17631867   PMID:17652086   PMID:17884806   PMID:17901998  
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PMID:19733651   PMID:19736351   PMID:19782967   PMID:19797898   PMID:19801490   PMID:19802002   PMID:19913121   PMID:19913623   PMID:19937977   PMID:19965935   PMID:19967439   PMID:20036336  
PMID:20061032   PMID:20102668   PMID:20215529   PMID:20218976   PMID:20227043   PMID:20371257   PMID:20374152   PMID:20379614   PMID:20427670   PMID:20435087   PMID:20467437   PMID:20472376  
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PMID:38175774   PMID:38224792   PMID:38262564   PMID:38331905   PMID:38355448   PMID:38369520  


Genomics

Comparative Map Data
NRG1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38831,639,245 - 32,774,046 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl831,639,222 - 32,855,666 (+)EnsemblGRCh38hg38GRCh38
GRCh37831,496,761 - 32,631,564 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36831,616,810 - 32,741,615 (+)NCBINCBI36Build 36hg18NCBI36
Build 34832,525,654 - 32,741,615NCBI
Celera830,430,833 - 31,581,276 (+)NCBICelera
Cytogenetic Map8p12NCBI
HuRef830,042,037 - 31,167,972 (+)NCBIHuRef
CHM1_1831,698,276 - 32,824,231 (+)NCBICHM1_1
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBIT2T-CHM13v2.0
Nrg1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39832,299,493 - 33,381,858 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl832,408,601 - 32,408,786 (-)EnsemblGRCm39 Ensembl
GRCm39 Ensembl832,304,579 - 33,374,825 (-)EnsemblGRCm39 Ensembl
GRCm38831,807,452 - 32,891,609 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl831,814,551 - 32,884,797 (-)EnsemblGRCm38mm10GRCm38
MGSCv37832,928,500 - 33,028,675 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36833,280,406 - 33,475,426 (-)NCBIMGSCv36mm8
Celera833,340,249 - 33,441,164 (-)NCBICelera
Cytogenetic Map8A3NCBI
cM Map818.75NCBI
Nrg1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81665,954,084 - 67,007,484 (+)NCBIGRCr8
mRatBN7.21659,250,658 - 60,304,519 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1659,250,854 - 60,296,884 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1664,587,755 - 65,638,290 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01668,001,434 - 69,052,009 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01663,221,979 - 64,273,342 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01662,969,573 - 64,065,063 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1663,837,216 - 64,057,434 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01662,632,432 - 63,718,738 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41663,937,796 - 64,126,183 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11663,937,870 - 64,126,262 (+)NCBI
Celera1657,283,140 - 58,311,856 (+)NCBICelera
Cytogenetic Map16q12.3NCBI
Nrg1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554638,009,530 - 9,037,116 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554638,009,436 - 9,037,116 (+)NCBIChiLan1.0ChiLan1.0
NRG1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2750,214,732 - 51,343,176 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1826,509,393 - 27,059,005 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0830,954,852 - 32,084,411 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1829,049,787 - 29,267,531 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl829,050,222 - 29,263,977 (+)Ensemblpanpan1.1panPan2
NRG1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11631,697,958 - 32,771,888 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1631,706,851 - 32,771,932 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1632,223,605 - 33,296,875 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01633,726,025 - 34,800,223 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1633,733,366 - 34,799,290 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11631,820,963 - 32,893,204 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01632,400,606 - 33,474,314 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01632,439,477 - 33,584,021 (-)NCBIUU_Cfam_GSD_1.0
Nrg1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494354,835,543 - 55,046,030 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367661,104,728 - 1,305,972 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367661,104,841 - 1,306,368 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NRG1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1552,630,679 - 52,839,505 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11552,625,550 - 53,688,003 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21559,915,458 - 59,983,046 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NRG1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1829,745,984 - 30,862,140 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl830,635,803 - 30,856,487 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605211,219,877 - 12,342,139 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nrg1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462478011,301,182 - 12,424,066 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462478011,297,306 - 11,525,236 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NRG1
92 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_013964.5(NRG1):c.332T>C (p.Met111Thr) single nucleotide variant Hereditary spastic paraplegia [RCV001376152] Chr8:32605615 [GRCh38]
Chr8:32463133 [GRCh37]
Chr8:8p12		 affects
GRCh38/hg38 8p23.1-11.21(chr8:12609975-42085703)x3 copy number gain See cases [RCV000050294] Chr8:12609975..42085703 [GRCh38]
Chr8:12467484..41943221 [GRCh37]
Chr8:12511855..42062378 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p12-q11.21(chr8:29719897-48521849)x3 copy number gain See cases [RCV000050995] Chr8:29719897..48521849 [GRCh38]
Chr8:29577413..49434409 [GRCh37]
Chr8:29633332..49596962 [NCBI36]
Chr8:8p12-q11.21		 pathogenic
GRCh38/hg38 8p21.2-q11.21(chr8:25832130-48521849)x3 copy number gain See cases [RCV000050904] Chr8:25832130..48521849 [GRCh38]
Chr8:25689646..49434409 [GRCh37]
Chr8:25745563..49596962 [NCBI36]
Chr8:8p21.2-q11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12728904-43673207)x3 copy number gain See cases [RCV000050912] Chr8:12728904..43673207 [GRCh38]
Chr8:12586413..43528350 [GRCh37]
Chr8:12630784..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12383584-36370018)x3 copy number gain See cases [RCV000051145] Chr8:12383584..36370018 [GRCh38]
Chr8:12241093..36227536 [GRCh37]
Chr8:12285464..36347088 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12728904-41928741)x3 copy number gain See cases [RCV000051110] Chr8:12728904..41928741 [GRCh38]
Chr8:12586413..41786259 [GRCh37]
Chr8:12630784..41905416 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43336172)x3 copy number gain See cases [RCV000053630] Chr8:12609975..43336172 [GRCh38]
Chr8:12467484..43191315 [GRCh37]
Chr8:12511855..43310472 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43255410)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053631]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053631]|See cases [RCV000053631] Chr8:12609975..43255410 [GRCh38]
Chr8:12467484..43110553 [GRCh37]
Chr8:12511855..43229710 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12750796-43532444)x3 copy number gain See cases [RCV000053632] Chr8:12750796..43532444 [GRCh38]
Chr8:12608305..43387587 [GRCh37]
Chr8:12652676..43506744 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3 copy number gain See cases [RCV000053635] Chr8:14940110..47929925 [GRCh38]
Chr8:14797619..48842485 [GRCh37]
Chr8:14841990..49005038 [NCBI36]
Chr8:8p22-q11.21		 pathogenic
GRCh38/hg38 8p23.1-11.23(chr8:12609975-37892000)x3 copy number gain See cases [RCV000053629] Chr8:12609975..37892000 [GRCh38]
Chr8:12467484..37749518 [GRCh37]
Chr8:12511855..37868676 [NCBI36]
Chr8:8p23.1-11.23		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
NM_013956.3(NRG1):c.1797C>T (p.Pro599=) single nucleotide variant Malignant melanoma [RCV000068292] Chr8:32764261 [GRCh38]
Chr8:32621779 [GRCh37]
Chr8:32741321 [NCBI36]
Chr8:8p12		 not provided
NM_013962.2(NRG1):c.745+19828T>C single nucleotide variant Lung cancer [RCV000107311] Chr8:31660557 [GRCh38]
Chr8:31518073 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013962.2(NRG1):c.745+100047C>A single nucleotide variant Lung cancer [RCV000107312] Chr8:31740776 [GRCh38]
Chr8:31598292 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013962.2(NRG1):c.745+146561G>C single nucleotide variant Lung cancer [RCV000107313] Chr8:31787290 [GRCh38]
Chr8:31644806 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013962.2(NRG1):c.746-399477C>T single nucleotide variant Lung cancer [RCV000107314] Chr8:32196353 [GRCh38]
Chr8:32053869 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013962.2(NRG1):c.746-139686A>G single nucleotide variant Lung cancer [RCV000107315] Chr8:32456144 [GRCh38]
Chr8:32313660 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013962.3(NRG1):c.11G>A (p.Arg4Gln) single nucleotide variant NRG1-related condition [RCV003952532]|not provided [RCV000084671] Chr8:31639995 [GRCh38]
Chr8:31497511 [GRCh37]
Chr8:8p12		 benign|not provided
NM_001159995.3(NRG1):c.37+564G>C single nucleotide variant not provided [RCV000084672] Chr8:31639995 [GRCh38]
Chr8:31497511 [GRCh37]
Chr8:8p12		 not provided
NM_013962.3(NRG1):c.26G>A (p.Arg9His) single nucleotide variant NRG1-related condition [RCV003952533]|not provided [RCV000084673] Chr8:31640010 [GRCh38]
Chr8:31497526 [GRCh37]
Chr8:8p12		 benign|not provided
NM_001159995.3(NRG1):c.37+596C>T single nucleotide variant not provided [RCV000084674] Chr8:31640027 [GRCh38]
Chr8:31497543 [GRCh37]
Chr8:8p12		 not provided
NM_001159995.3(NRG1):c.37+661G>A single nucleotide variant not provided [RCV000084675] Chr8:31640092 [GRCh38]
Chr8:31497608 [GRCh37]
Chr8:8p12		 not provided
NM_001159995.3(NRG1):c.37+676C>A single nucleotide variant not provided [RCV000084676] Chr8:31640107 [GRCh38]
Chr8:31497623 [GRCh37]
Chr8:8p12		 not provided
NM_001159995.3(NRG1):c.37+744C>T single nucleotide variant not provided [RCV000084677] Chr8:31640175 [GRCh38]
Chr8:31497691 [GRCh37]
Chr8:8p12		 not provided
NM_001159995.3(NRG1):c.37+865G>A single nucleotide variant not provided [RCV000084678] Chr8:31640296 [GRCh38]
Chr8:31497812 [GRCh37]
Chr8:8p12		 likely benign|not provided
NM_001159995.3(NRG1):c.37+903C>T single nucleotide variant not provided [RCV000084679] Chr8:31640334 [GRCh38]
Chr8:31497850 [GRCh37]
Chr8:8p12		 not provided
NM_001159995.3(NRG1):c.37+913G>T single nucleotide variant not provided [RCV000084680] Chr8:31640344 [GRCh38]
Chr8:31497860 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.30A>C (p.Lys10Asn) single nucleotide variant not provided [RCV000084681] Chr8:32548756 [GRCh38]
Chr8:32406274 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.140C>T (p.Ser47Leu) single nucleotide variant not provided [RCV000084682] Chr8:32595867 [GRCh38]
Chr8:32453385 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.679A>G (p.Met227Val) single nucleotide variant not provided [RCV000084683] Chr8:32742054 [GRCh38]
Chr8:32599572 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.819G>T (p.Lys273Asn) single nucleotide variant not provided [RCV000084684] Chr8:32756418 [GRCh38]
Chr8:32613936 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.835C>G (p.Arg279Gly) single nucleotide variant not provided [RCV000084685] Chr8:32756434 [GRCh38]
Chr8:32613952 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.857G>A (p.Arg286Gln) single nucleotide variant not provided [RCV000084686] Chr8:32756456 [GRCh38]
Chr8:32613974 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.893A>G (p.His298Arg) single nucleotide variant not provided [RCV000084687] Chr8:32756492 [GRCh38]
Chr8:32614010 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.1005T>C (p.Ser335=) single nucleotide variant not provided [RCV000084688] Chr8:32759380 [GRCh38]
Chr8:32616898 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.1322C>T (p.Thr441Met) single nucleotide variant not provided [RCV000084689] Chr8:32763801 [GRCh38]
Chr8:32621319 [GRCh37]
Chr8:8p12		 not provided
NM_013964.5(NRG1):c.1538C>T (p.Pro513Leu) single nucleotide variant not provided [RCV000084690] Chr8:32764017 [GRCh38]
Chr8:32621535 [GRCh37]
Chr8:8p12		 not provided
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43673207)x3 copy number gain See cases [RCV000135786] Chr8:12609975..43673207 [GRCh38]
Chr8:12467484..43528350 [GRCh37]
Chr8:12511855..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12383584-43673207)x3 copy number gain See cases [RCV000135566] Chr8:12383584..43673207 [GRCh38]
Chr8:12241093..43528350 [GRCh37]
Chr8:12285464..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12728904-40169194)x3 copy number gain See cases [RCV000136516] Chr8:12728904..40169194 [GRCh38]
Chr8:12586413..40026713 [GRCh37]
Chr8:12630784..40145870 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p12(chr8:31750519-32478810)x3 copy number gain See cases [RCV000136062] Chr8:31750519..32478810 [GRCh38]
Chr8:31608035..32336326 [GRCh37]
Chr8:31727577..32455868 [NCBI36]
Chr8:8p12		 uncertain significance
GRCh38/hg38 8p12-11.21(chr8:29362097-40231708)x1 copy number loss See cases [RCV000136878] Chr8:29362097..40231708 [GRCh38]
Chr8:29219614..40089227 [GRCh37]
Chr8:29275533..40208384 [NCBI36]
Chr8:8p12-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12182421-43673207)x3 copy number gain See cases [RCV000137249] Chr8:12182421..43673207 [GRCh38]
Chr8:12039930..43528350 [GRCh37]
Chr8:12077339..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12698495-35476082)x3 copy number gain See cases [RCV000138058] Chr8:12698495..35476082 [GRCh38]
Chr8:12556004..35333600 [GRCh37]
Chr8:12600375..35453142 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p21.2-12(chr8:25171103-31750600)x1 copy number loss See cases [RCV000138081] Chr8:25171103..31750600 [GRCh38]
Chr8:25028618..31608116 [GRCh37]
Chr8:25084535..31727658 [NCBI36]
Chr8:8p21.2-12		 pathogenic
NM_013964.5(NRG1):c.502+31229G>C single nucleotide variant not specified [RCV000202884] Chr8:32648114 [GRCh38]
Chr8:32505633 [GRCh37]
Chr8:8p12		 likely benign
GRCh38/hg38 8p23.3-11.23(chr8:226452-38021728)x3 copy number gain See cases [RCV000137807] Chr8:226452..38021728 [GRCh38]
Chr8:176452..37879246 [GRCh37]
Chr8:166452..37998403 [NCBI36]
Chr8:8p23.3-11.23		 pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p12(chr8:30368765-36421541)x3 copy number gain See cases [RCV000139926] Chr8:30368765..36421541 [GRCh38]
Chr8:30226281..36279059 [GRCh37]
Chr8:30345823..36398222 [NCBI36]
Chr8:8p12		 uncertain significance
GRCh38/hg38 8p23.1-11.22(chr8:7141697-38695546)x3 copy number gain See cases [RCV000139891] Chr8:7141697..38695546 [GRCh38]
Chr8:6999219..38553064 [GRCh37]
Chr8:6986629..38672221 [NCBI36]
Chr8:8p23.1-11.22		 pathogenic
GRCh38/hg38 8p23.1-11.22(chr8:12729023-39235934)x3 copy number gain See cases [RCV000139770] Chr8:12729023..39235934 [GRCh38]
Chr8:12586532..39093453 [GRCh37]
Chr8:12630903..39212610 [NCBI36]
Chr8:8p23.1-11.22		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12646123-43686843)x3 copy number gain See cases [RCV000139796] Chr8:12646123..43686843 [GRCh38]
Chr8:12503632..43541986 [GRCh37]
Chr8:12548003..43661143 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.23(chr8:11851113-37216333)x3 copy number gain See cases [RCV000139549] Chr8:11851113..37216333 [GRCh38]
Chr8:11708622..37073851 [GRCh37]
Chr8:11746031..37193009 [NCBI36]
Chr8:8p23.1-11.23		 pathogenic
GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3 copy number gain See cases [RCV000141410] Chr8:226452..34491890 [GRCh38]
Chr8:176452..34349408 [GRCh37]
Chr8:166452..34468950 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p12(chr8:32713114-33352866)x1 copy number loss See cases [RCV000141376] Chr8:32713114..33352866 [GRCh38]
Chr8:32570632..33210384 [GRCh37]
Chr8:32690174..33329926 [NCBI36]
Chr8:8p12		 uncertain significance
GRCh38/hg38 8p12(chr8:31847822-31868891)x1 copy number loss See cases [RCV000140872] Chr8:31847822..31868891 [GRCh38]
Chr8:31705338..31726407 [GRCh37]
Chr8:31824880..31845949 [NCBI36]
Chr8:8p12		 likely benign
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p12(chr8:30958352-32189009)x3 copy number gain See cases [RCV000142168] Chr8:30958352..32189009 [GRCh38]
Chr8:30815868..32046525 [GRCh37]
Chr8:30935410..32166067 [NCBI36]
Chr8:8p12		 likely benign|uncertain significance
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p22-12(chr8:18972996-33619264)x1 copy number loss See cases [RCV000142747] Chr8:18972996..33619264 [GRCh38]
Chr8:18830506..33476782 [GRCh37]
Chr8:18874786..33596324 [NCBI36]
Chr8:8p22-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12633490-40685533)x3 copy number gain See cases [RCV000143508] Chr8:12633490..40685533 [GRCh38]
Chr8:12490999..40543052 [GRCh37]
Chr8:12535370..40662209 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12609975-42085703)x3 copy number gain See cases [RCV000148249] Chr8:12609975..42085703 [GRCh38]
Chr8:12467484..41943221 [GRCh37]
Chr8:12511855..42062378 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12728904-43673207)x3 copy number gain See cases [RCV000148237] Chr8:12728904..43673207 [GRCh38]
Chr8:12586413..43528350 [GRCh37]
Chr8:12630784..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p23.1-11.22(chr8:12528482-39593802)x3 copy number gain See cases [RCV000511325] Chr8:12528482..39593802 [GRCh37]
Chr8:8p23.1-11.22		 pathogenic
GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3 copy number gain See cases [RCV000446588] Chr8:24772064..24813176 [GRCh37]
Chr8:8p21.2-q12.1		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-11.1(chr8:158048-43786723)x3 copy number gain See cases [RCV000447909] Chr8:158048..43786723 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
GRCh37/hg19 8p23.1-11.1(chr8:12580132-43388233)x3 copy number gain See cases [RCV000447913] Chr8:12580132..43388233 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p21.2-12(chr8:24514488-34808438) copy number gain See cases [RCV000448582] Chr8:24514488..34808438 [GRCh37]
Chr8:8p21.2-12		 pathogenic
GRCh37/hg19 8p22-12(chr8:16992973-32612724)x1 copy number loss not provided [RCV000509389] Chr8:16992973..32612724 [GRCh37]
Chr8:8p22-12		 not provided
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12528482-33684786)x3 copy number gain See cases [RCV000510571] Chr8:12528482..33684786 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.1-11.1(chr8:11935023-43824035)x3 copy number gain See cases [RCV000511028] Chr8:11935023..43824035 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:11945855-34875355)x3 copy number gain See cases [RCV000510899] Chr8:11945855..34875355 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3		 pathogenic
GRCh37/hg19 8p12(chr8:32356612-32908980)x1 copy number loss not provided [RCV000682983] Chr8:32356612..32908980 [GRCh37]
Chr8:8p12		 uncertain significance
GRCh37/hg19 8p12-11.21(chr8:31352498-41481295)x3 copy number gain not provided [RCV000683035] Chr8:31352498..41481295 [GRCh37]
Chr8:8p12-11.21		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12552775-35935825)x3 copy number gain not provided [RCV000683043] Chr8:12552775..35935825 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p12(chr8:30335124-33770070)x1 copy number loss not provided [RCV000683024] Chr8:30335124..33770070 [GRCh37]
Chr8:8p12		 pathogenic
GRCh37/hg19 8p12(chr8:29103983-35728509)x1 copy number loss not provided [RCV000846377] Chr8:29103983..35728509 [GRCh37]
Chr8:8p12		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12556004-34374150)x3 copy number gain not provided [RCV000762735] Chr8:12556004..34374150 [GRCh37]
Chr8:8p23.1-12		 likely pathogenic
NM_013964.5(NRG1):c.1365C>T (p.Pro455=) single nucleotide variant NRG1-related condition [RCV003930628]|not provided [RCV000884820] Chr8:32763844 [GRCh38]
Chr8:32621362 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.162C>T (p.Val54=) single nucleotide variant not provided [RCV000925510] Chr8:32595889 [GRCh38]
Chr8:32453407 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1104C>T (p.His368=) single nucleotide variant not provided [RCV000924079] Chr8:32760242 [GRCh38]
Chr8:32617760 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1095C>T (p.Ser365=) single nucleotide variant not provided [RCV000926791] Chr8:32760233 [GRCh38]
Chr8:32617751 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1634G>A (p.Arg545Gln) single nucleotide variant NRG1-related condition [RCV003972880]|not provided [RCV000968623] Chr8:32764113 [GRCh38]
Chr8:32621631 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.141G>A (p.Ser47=) single nucleotide variant not provided [RCV000925950] Chr8:32595868 [GRCh38]
Chr8:32453386 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.282G>A (p.Lys94=) single nucleotide variant not provided [RCV000915426] Chr8:32605565 [GRCh38]
Chr8:32463083 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1232C>G (p.Thr411Ser) single nucleotide variant NRG1-related condition [RCV003910808]|not provided [RCV000904797] Chr8:32760370 [GRCh38]
Chr8:32617888 [GRCh37]
Chr8:8p12		 benign|likely benign
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3		 pathogenic
Single allele duplication not provided [RCV000768452] Chr8:12546855..35816855 [GRCh37]
Chr8:8p23.1-12		 likely pathogenic
NM_013964.5(NRG1):c.1380G>A (p.Thr460=) single nucleotide variant NRG1-related condition [RCV003978001]|not provided [RCV000915123] Chr8:32763859 [GRCh38]
Chr8:32621377 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.414T>C (p.Gly138=) single nucleotide variant NRG1-related condition [RCV003905840]|not provided [RCV000961861] Chr8:32614527 [GRCh38]
Chr8:32472045 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.1246C>T (p.Arg416Ter) single nucleotide variant not provided [RCV000999023] Chr8:32760384 [GRCh38]
Chr8:32617902 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013964.5(NRG1):c.233A>T (p.Asn78Ile) single nucleotide variant Inborn genetic diseases [RCV002550731]|not provided [RCV000999022] Chr8:32595960 [GRCh38]
Chr8:32453478 [GRCh37]
Chr8:8p12		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p12(chr8:32612883-32834544)x3 copy number gain not provided [RCV001006095] Chr8:32612883..32834544 [GRCh37]
Chr8:8p12		 uncertain significance
GRCh37/hg19 8p12(chr8:31005298-32056029)x3 copy number gain not provided [RCV001006094] Chr8:31005298..32056029 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013964.5(NRG1):c.1158G>T (p.Gly386=) single nucleotide variant not provided [RCV000982671] Chr8:32760296 [GRCh38]
Chr8:32617814 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.600A>G (p.Lys200=) single nucleotide variant not provided [RCV000916384] Chr8:32728046 [GRCh38]
Chr8:32585564 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1633C>T (p.Arg545Trp) single nucleotide variant not provided [RCV001702147]|not specified [RCV001726670] Chr8:32764112 [GRCh38]
Chr8:32621630 [GRCh37]
Chr8:8p12		 benign|likely benign
GRCh37/hg19 8p12(chr8:31406614-32010201)x4 copy number gain not provided [RCV002473678] Chr8:31406614..32010201 [GRCh37]
Chr8:8p12		 uncertain significance
NM_013964.5(NRG1):c.781G>T (p.Val261Leu) single nucleotide variant not specified [RCV001703389] Chr8:32754452 [GRCh38]
Chr8:32611970 [GRCh37]
Chr8:8p12		 benign
GRCh37/hg19 8p23.3-11.1(chr8:176814-43396776) copy number gain Abnormal fetal cardiovascular morphology [RCV001291977] Chr8:176814..43396776 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
NM_013964.5(NRG1):c.1062-5C>T single nucleotide variant NRG1-related condition [RCV003968492]|not specified [RCV001703267] Chr8:32760195 [GRCh38]
Chr8:32617713 [GRCh37]
Chr8:8p12		 benign
NM_001159995.3(NRG1):c.37+725G>A single nucleotide variant not provided [RCV001797340] Chr8:31640156 [GRCh38]
Chr8:31497672 [GRCh37]
Chr8:8p12		 benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771) copy number gain Polydactyly [RCV002280629] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
Single allele complex See cases [RCV002292428] Chr8:6999114..11935023 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
Single allele complex 8p inverted duplication/deletion syndrome [RCV002280753] Chr8:158048..43019304 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p21.2-11.22(chr8:26808969-38346383)x1 copy number loss not provided [RCV002472596] Chr8:26808969..38346383 [GRCh37]
Chr8:8p21.2-11.22		 pathogenic
Single allele duplication not provided [RCV003448693] Chr8:12530550..43483193 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p23.1-11.23(chr8:11945856-37902453)x3 copy number gain not provided [RCV003484722] Chr8:11945856..37902453 [GRCh37]
Chr8:8p23.1-11.23		 pathogenic
GRCh37/hg19 8p23.2-11.21(chr8:2201405-41723095)x3 copy number gain not provided [RCV003484713] Chr8:2201405..41723095 [GRCh37]
Chr8:8p23.2-11.21		 pathogenic
GRCh37/hg19 8p23.1-11.22(chr8:12560782-38748763)x3 copy number gain not provided [RCV003484724] Chr8:12560782..38748763 [GRCh37]
Chr8:8p23.1-11.22		 pathogenic
GRCh37/hg19 8p22-11.1(chr8:14240573-43824035)x3 copy number gain not provided [RCV003484725] Chr8:14240573..43824035 [GRCh37]
Chr8:8p22-11.1		 pathogenic
NM_013964.5(NRG1):c.502+31211G>C single nucleotide variant NRG1-related condition [RCV003966430]|not provided [RCV003436852] Chr8:32648096 [GRCh38]
Chr8:32505615 [GRCh37]
Chr8:8p12		 benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not specified [RCV003986742] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p21.3-11.1(chr8:20136266-43786723)x3 copy number gain not specified [RCV003986767] Chr8:20136266..43786723 [GRCh37]
Chr8:8p21.3-11.1		 pathogenic
GRCh37/hg19 8p23.3-11.21(chr8:158048-41600696)x3 copy number gain not specified [RCV003986756] Chr8:158048..41600696 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3 copy number gain not specified [RCV003986754] Chr8:27024288..89410121 [GRCh37]
Chr8:8p21.2-q21.3		 pathogenic
NM_001159995.3(NRG1):c.37+853GGC[4] microsatellite NRG1-related condition [RCV003919568] Chr8:31640284..31640286 [GRCh38]
Chr8:31497800..31497802 [GRCh37]
Chr8:8p12		 likely benign
NM_013962.3(NRG1):c.224T>C (p.Leu75Pro) single nucleotide variant NRG1-related condition [RCV003964375] Chr8:31640208 [GRCh38]
Chr8:31497724 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.113G>A (p.Arg38Gln) single nucleotide variant NRG1-related condition [RCV003974300] Chr8:32595840 [GRCh38]
Chr8:32453358 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.502+30968G>A single nucleotide variant NRG1-related condition [RCV003984552] Chr8:32647853 [GRCh38]
Chr8:32505372 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.1640C>T (p.Ala547Val) single nucleotide variant NRG1-related condition [RCV003931384] Chr8:32764119 [GRCh38]
Chr8:32621637 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.1096G>A (p.Glu366Lys) single nucleotide variant NRG1-related condition [RCV003931712] Chr8:32760234 [GRCh38]
Chr8:32617752 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.1062-4G>A single nucleotide variant NRG1-related condition [RCV003931741] Chr8:32760196 [GRCh38]
Chr8:32617714 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.502+30933C>A single nucleotide variant NRG1-related condition [RCV003922231] Chr8:32647818 [GRCh38]
Chr8:32505337 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.1808C>A (p.Pro603His) single nucleotide variant NRG1-related condition [RCV003921976] Chr8:32764287 [GRCh38]
Chr8:32621805 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.1847G>T (p.Gly616Val) single nucleotide variant NRG1-related condition [RCV003979793] Chr8:32764326 [GRCh38]
Chr8:32621844 [GRCh37]
Chr8:8p12		 benign
NM_013964.5(NRG1):c.111C>G (p.Pro37=) single nucleotide variant NRG1-related condition [RCV003924208] Chr8:32595838 [GRCh38]
Chr8:32453356 [GRCh37]
Chr8:8p12		 likely benign
NM_013962.3(NRG1):c.15C>G (p.Arg5=) single nucleotide variant NRG1-related condition [RCV003941656] Chr8:31639999 [GRCh38]
Chr8:31497515 [GRCh37]
Chr8:8p12		 likely benign
NM_013964.5(NRG1):c.866T>C (p.Met289Thr) single nucleotide variant NRG1-related condition [RCV003982045] Chr8:32756465 [GRCh38]
Chr8:32613983 [GRCh37]
Chr8:8p12		 benign
NM_013962.3(NRG1):c.473C>T (p.Ala158Val) single nucleotide variant NRG1-related condition [RCV003976406] Chr8:31640457 [GRCh38]
Chr8:31497973 [GRCh37]
Chr8:8p12		 benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5419
Count of miRNA genes:1073
Interacting mature miRNAs:1315
Transcripts:ENST00000287842, ENST00000287845, ENST00000338921, ENST00000341377, ENST00000356819, ENST00000405005, ENST00000518084, ENST00000518104, ENST00000518206, ENST00000519240, ENST00000519301, ENST00000520407, ENST00000520502, ENST00000521670, ENST00000522402, ENST00000522569, ENST00000523041, ENST00000523079, ENST00000523534, ENST00000523681, ENST00000539990
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.

Markers in Region
D8S499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,141,955 - 32,142,089UniSTSGRCh37
Build 36832,261,497 - 32,261,631RGDNCBI36
Celera831,100,433 - 31,100,563RGD
Cytogenetic Map8p12UniSTS
HuRef830,687,120 - 30,687,254UniSTS
Marshfield Genetic Map860.34UniSTS
Marshfield Genetic Map860.34RGD
D8S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,067,167 - 32,067,336UniSTSGRCh37
Build 36832,186,709 - 32,186,878RGDNCBI36
Celera831,025,648 - 31,025,813RGD
Cytogenetic Map8p12UniSTS
HuRef830,612,326 - 30,612,495UniSTS
Marshfield Genetic Map860.34UniSTS
Marshfield Genetic Map860.34RGD
D8S375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,457,820 - 32,457,947UniSTSGRCh37
Build 36832,577,362 - 32,577,489RGDNCBI36
Celera831,416,545 - 31,416,672RGD
Cytogenetic Map8p12UniSTS
HuRef831,002,964 - 31,003,091UniSTS
Marshfield Genetic Map860.34UniSTS
Marshfield Genetic Map860.34RGD
deCODE Assembly Map853.36UniSTS
D8S1125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,367,516 - 32,367,741UniSTSGRCh37
Build 36832,487,058 - 32,487,283RGDNCBI36
Celera831,326,045 - 31,326,271RGD
Cytogenetic Map8p12UniSTS
HuRef830,912,628 - 30,912,862UniSTS
Marshfield Genetic Map860.34UniSTS
Marshfield Genetic Map860.34RGD
Whitehead-YAC Contig Map8 UniSTS
D8S278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,548,387 - 32,548,534UniSTSGRCh37
GRCh37832,548,390 - 32,548,625UniSTSGRCh37
Build 36832,667,932 - 32,668,167RGDNCBI36
Celera831,507,117 - 31,507,352RGD
Celera831,507,114 - 31,507,261UniSTS
Cytogenetic Map8p12UniSTS
HuRef831,093,402 - 31,093,637UniSTS
HuRef831,093,399 - 31,093,546UniSTS
Marshfield Genetic Map860.87RGD
Genethon Genetic Map860.0UniSTS
TNG Radiation Hybrid Map818931.0UniSTS
deCODE Assembly Map853.64UniSTS
Stanford-G3 RH Map81473.0UniSTS
GeneMap99-GB4 RH Map8122.12UniSTS
Whitehead-RH Map8125.6UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map8453.4UniSTS
GeneMap99-G3 RH Map81563.0UniSTS
D8S1810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,691,721 - 31,691,905UniSTSGRCh37
Build 36831,811,263 - 31,811,447RGDNCBI36
Celera830,650,016 - 30,650,218RGD
Cytogenetic Map8p12UniSTS
Cytogenetic Map8qUniSTS
HuRef830,236,744 - 30,236,944UniSTS
Marshfield Genetic Map860.34UniSTS
Marshfield Genetic Map860.34RGD
Genethon Genetic Map859.4UniSTS
deCODE Assembly Map852.98UniSTS
Whitehead-YAC Contig Map8 UniSTS
G27359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,512,307 - 31,512,456UniSTSGRCh37
Build 36831,631,849 - 31,631,998RGDNCBI36
Celera830,471,196 - 30,471,345RGD
Cytogenetic Map8p12UniSTS
HuRef830,057,583 - 30,057,732UniSTS
RH11877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,559,068 - 31,559,233UniSTSGRCh37
Build 36831,678,610 - 31,678,775RGDNCBI36
Celera830,517,911 - 30,518,076RGD
Cytogenetic Map8p12UniSTS
HuRef830,104,366 - 30,104,531UniSTS
GeneMap99-GB4 RH Map8122.12UniSTS
NCBI RH Map8411.3UniSTS
WI-18803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,600,306 - 32,600,452UniSTSGRCh37
Build 36832,719,848 - 32,719,994RGDNCBI36
Celera831,559,019 - 31,559,165RGD
Cytogenetic Map8p12UniSTS
HuRef831,145,709 - 31,145,855UniSTS
GeneMap99-GB4 RH Map8119.69UniSTS
Whitehead-RH Map8124.7UniSTS
RH65488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,566,731 - 31,566,852UniSTSGRCh37
Build 36831,686,273 - 31,686,394RGDNCBI36
Celera830,525,573 - 30,525,694RGD
Cytogenetic Map8p12UniSTS
HuRef830,112,028 - 30,112,149UniSTS
GeneMap99-GB4 RH Map8121.8UniSTS
NCBI RH Map8411.3UniSTS
RH98441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,996,819 - 31,996,954UniSTSGRCh37
Build 36832,116,361 - 32,116,496RGDNCBI36
Celera830,955,269 - 30,955,404RGD
Cytogenetic Map8p12UniSTS
HuRef830,541,943 - 30,542,078UniSTS
GeneMap99-GB4 RH Map8122.12UniSTS
SHGC-82537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,412,407 - 32,412,725UniSTSGRCh37
Build 36832,531,949 - 32,532,267RGDNCBI36
Celera831,371,128 - 31,371,448RGD
Cytogenetic Map8p12UniSTS
HuRef830,957,547 - 30,957,867UniSTS
TNG Radiation Hybrid Map817820.0UniSTS
SHGC-78993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,966,483 - 31,966,761UniSTSGRCh37
Build 36832,086,025 - 32,086,303RGDNCBI36
Celera830,924,931 - 30,925,209RGD
Cytogenetic Map8p12UniSTS
HuRef830,511,609 - 30,511,887UniSTS
TNG Radiation Hybrid Map817509.0UniSTS
SHGC-81230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,490,377 - 32,490,678UniSTSGRCh37
Build 36832,609,919 - 32,610,220RGDNCBI36
Celera831,449,102 - 31,449,403RGD
Cytogenetic Map8p12UniSTS
HuRef831,035,539 - 31,035,840UniSTS
TNG Radiation Hybrid Map817775.0UniSTS
SHGC-80823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,289,160 - 32,289,479UniSTSGRCh37
Build 36832,408,702 - 32,409,021RGDNCBI36
Celera831,247,661 - 31,247,980RGD
Cytogenetic Map8p12UniSTS
HuRef830,834,268 - 30,834,587UniSTS
TNG Radiation Hybrid Map817933.0UniSTS
RH119663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,010,416 - 32,010,688UniSTSGRCh37
Build 36832,129,958 - 32,130,230RGDNCBI36
Celera830,968,865 - 30,969,137RGD
Cytogenetic Map8p12UniSTS
HuRef830,555,539 - 30,555,811UniSTS
TNG Radiation Hybrid Map817492.0UniSTS
RH120019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,561,336 - 31,561,646UniSTSGRCh37
Build 36831,680,878 - 31,681,188RGDNCBI36
Celera830,520,179 - 30,520,489RGD
Cytogenetic Map8p12UniSTS
HuRef830,106,633 - 30,106,943UniSTS
TNG Radiation Hybrid Map816992.0UniSTS
RH120054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,289,029 - 32,289,351UniSTSGRCh37
Build 36832,408,571 - 32,408,893RGDNCBI36
Celera831,247,530 - 31,247,852RGD
Cytogenetic Map8p12UniSTS
HuRef830,834,137 - 30,834,459UniSTS
TNG Radiation Hybrid Map817943.0UniSTS
RH122857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,579,336 - 32,579,663UniSTSGRCh37
Build 36832,698,878 - 32,699,205RGDNCBI36
Celera831,538,051 - 31,538,378RGD
Cytogenetic Map8p12UniSTS
HuRef831,124,750 - 31,125,077UniSTS
TNG Radiation Hybrid Map818896.0UniSTS
RH123550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,696,861 - 31,697,168UniSTSGRCh37
Build 36831,816,403 - 31,816,710RGDNCBI36
Celera830,655,174 - 30,655,481RGD
Cytogenetic Map8p12UniSTS
HuRef830,241,900 - 30,242,207UniSTS
TNG Radiation Hybrid Map817416.0UniSTS
G59016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,500,109 - 31,500,383UniSTSGRCh37
Build 36831,619,651 - 31,619,925RGDNCBI36
Celera830,459,008 - 30,459,282RGD
Cytogenetic Map8p12UniSTS
HuRef830,045,327 - 30,045,601UniSTS
TNG Radiation Hybrid Map817048.0UniSTS
G63290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,399,668 - 32,400,007UniSTSGRCh37
Build 36832,519,210 - 32,519,549RGDNCBI36
Celera831,358,395 - 31,358,734RGD
Cytogenetic Map8p12UniSTS
HuRef830,944,993 - 30,945,332UniSTS
TNG Radiation Hybrid Map817745.0UniSTS
G63471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,166,680 - 32,166,971UniSTSGRCh37
Build 36832,286,222 - 32,286,513RGDNCBI36
Celera831,125,147 - 31,125,438RGD
Cytogenetic Map8p12UniSTS
HuRef830,711,731 - 30,712,022UniSTS
SHGC-142477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,770,022 - 31,770,298UniSTSGRCh37
Build 36831,889,564 - 31,889,840RGDNCBI36
Celera830,728,335 - 30,728,610RGD
Cytogenetic Map8p12UniSTS
HuRef830,315,076 - 30,315,350UniSTS
TNG Radiation Hybrid Map817347.0UniSTS
SHGC-142734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,770,022 - 31,770,307UniSTSGRCh37
Build 36831,889,564 - 31,889,849RGDNCBI36
Celera830,728,335 - 30,728,619RGD
Cytogenetic Map8p12UniSTS
HuRef830,315,076 - 30,315,359UniSTS
TNG Radiation Hybrid Map817368.0UniSTS
SHGC-142912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,953,529 - 31,953,800UniSTSGRCh37
Build 36832,073,071 - 32,073,342RGDNCBI36
Celera830,911,972 - 30,912,243RGD
Cytogenetic Map8p12UniSTS
HuRef830,498,650 - 30,498,921UniSTS
TNG Radiation Hybrid Map817543.0UniSTS
G17227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,476,763 - 32,476,947UniSTSGRCh37
Build 36832,596,305 - 32,596,489RGDNCBI36
Celera831,435,489 - 31,435,673RGD
Cytogenetic Map8p12UniSTS
HuRef831,021,926 - 31,022,110UniSTS
AFMA143YG9  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,978,855 - 31,978,978UniSTSGRCh37
Build 36832,098,397 - 32,098,520RGDNCBI36
Celera830,937,303 - 30,937,426RGD
Cytogenetic Map8p12UniSTS
HuRef830,523,981 - 30,524,104UniSTS
Whitehead-YAC Contig Map8 UniSTS
UniSTS:468010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,498,025 - 31,498,224UniSTSGRCh37
Build 36831,617,567 - 31,617,766RGDNCBI36
Celera830,456,924 - 30,457,123RGD
HuRef830,043,242 - 30,043,441UniSTS
D8S2226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,765,811 - 31,766,038UniSTSGRCh37
Build 36831,885,353 - 31,885,580RGDNCBI36
Celera830,724,124 - 30,724,351RGD
HuRef830,310,865 - 30,311,092UniSTS
RH35824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,600,461 - 32,600,650UniSTSGRCh37
Build 36832,720,003 - 32,720,192RGDNCBI36
Celera831,559,174 - 31,559,363RGD
Cytogenetic Map8p12UniSTS
HuRef831,145,864 - 31,146,053UniSTS
GeneMap99-GB4 RH Map8121.94UniSTS
HSC1IA022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,899,591 - 31,899,796UniSTSGRCh37
Build 36832,019,133 - 32,019,338RGDNCBI36
Celera830,858,052 - 30,858,257RGD
Cytogenetic Map8p12UniSTS
HuRef830,444,763 - 30,444,968UniSTS
GeneMap99-GB4 RH Map8124.51UniSTS
Whitehead-RH Map8125.5UniSTS
NCBI RH Map8411.3UniSTS
STS-Z40930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,203,989 - 32,204,057UniSTSGRCh37
Build 36832,323,531 - 32,323,599RGDNCBI36
Celera831,162,441 - 31,162,509RGD
Cytogenetic Map8p12UniSTS
HuRef830,749,092 - 30,749,160UniSTS
GeneMap99-GB4 RH Map8119.9UniSTS
SHGC-12780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,600,308 - 32,600,650UniSTSGRCh37
Build 36832,719,850 - 32,720,192RGDNCBI36
Celera831,559,021 - 31,559,363RGD
Cytogenetic Map8p12UniSTS
HuRef831,145,711 - 31,146,053UniSTS
Stanford-G3 RH Map81479.0UniSTS
NCBI RH Map8456.8UniSTS
GeneMap99-G3 RH Map81569.0UniSTS
D8S2063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,584,352 - 31,584,446UniSTSGRCh37
Build 36831,703,894 - 31,703,988RGDNCBI36
Celera830,542,818 - 30,542,912RGD
Cytogenetic Map8p12UniSTS
HuRef830,129,282 - 30,129,376UniSTS
G30982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37832,194,937 - 32,195,066UniSTSGRCh37
Build 36832,314,479 - 32,314,608RGDNCBI36
Celera831,153,400 - 31,153,529RGD
Cytogenetic Map8p12UniSTS
HuRef830,740,453 - 30,740,582UniSTS
L30054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37831,936,621 - 31,937,271UniSTSGRCh37
Celera830,895,071 - 30,895,733UniSTS
Cytogenetic Map8p12UniSTS
HuRef830,481,746 - 30,482,408UniSTS
D8S278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8p12UniSTS
Marshfield Genetic Map860.87UniSTS
Genethon Genetic Map860.0UniSTS
deCODE Assembly Map853.64UniSTS
GeneMap99-GB4 RH Map8122.12UniSTS
Whitehead-RH Map8125.6UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map8411.3UniSTS


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 adipose tissue appendage
High
Medium 12 45 9 3 12 24 24 73 41 62 99 7 6
Low 767 902 1301 459 671 310 2216 59 2421 303 1052 1417 152 33 1381
Below cutoff 1557 2056 345 126 699 114 1803 1839 1213 62 298 75 12 1128 1160

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001159995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001159996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001159999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160004 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001160008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013958 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013960 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005273486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005273487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013369 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013371 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB451331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB451475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC022833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC022850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC023948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC068359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC068931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC083977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104000 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC113209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF026146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF176921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF491780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY207002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC064587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK000383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ018711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA429204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN603652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN603654 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN603661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR450288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA805080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC425692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF372273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF372274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF372275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF372276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF372277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF517295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF517296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF517297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU359055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU363508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU363509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU363510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ983557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ983558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458729 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L12260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L12261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L41827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M94165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M94166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M94167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M94168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272758 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272759 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272775 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OQ272776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S68256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000287842   ⟹   ENSP00000287842
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,635 - 32,764,407 (+)Ensembl
RefSeq Acc Id: ENST00000356819   ⟹   ENSP00000349275
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,267 - 32,767,959 (+)Ensembl
RefSeq Acc Id: ENST00000405005   ⟹   ENSP00000384620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,311 - 32,774,046 (+)Ensembl
RefSeq Acc Id: ENST00000517967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,171,382 - 32,287,566 (+)Ensembl
RefSeq Acc Id: ENST00000518084   ⟹   ENSP00000428546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,721,753 - 32,754,423 (+)Ensembl
RefSeq Acc Id: ENST00000518206   ⟹   ENSP00000432052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,605,648 - 32,743,224 (+)Ensembl
RefSeq Acc Id: ENST00000519240   ⟹   ENSP00000428411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,721,845 - 32,756,475 (+)Ensembl
RefSeq Acc Id: ENST00000519301   ⟹   ENSP00000429582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,222 - 32,764,405 (+)Ensembl
RefSeq Acc Id: ENST00000520407   ⟹   ENSP00000434640
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,755 - 32,743,224 (+)Ensembl
RefSeq Acc Id: ENST00000520502   ⟹   ENSP00000433289
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,647,103 - 32,743,207 (+)Ensembl
RefSeq Acc Id: ENST00000521670   ⟹   ENSP00000428828
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,619 - 32,763,998 (+)Ensembl
RefSeq Acc Id: ENST00000522402   ⟹   ENSP00000430862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,721,819 - 32,763,794 (+)Ensembl
RefSeq Acc Id: ENST00000522569   ⟹   ENSP00000500194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,614,375 - 32,756,528 (+)Ensembl
RefSeq Acc Id: ENST00000523041   ⟹   ENSP00000433350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,647,103 - 32,743,221 (+)Ensembl
RefSeq Acc Id: ENST00000523079   ⟹   ENSP00000430120
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,210 - 32,760,989 (+)Ensembl
RefSeq Acc Id: ENST00000523320
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,220,928 - 32,287,447 (+)Ensembl
RefSeq Acc Id: ENST00000523534   ⟹   ENSP00000429067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,640,426 - 32,764,776 (+)Ensembl
RefSeq Acc Id: ENST00000523681
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,748,824 - 32,751,155 (+)Ensembl
RefSeq Acc Id: ENST00000539990   ⟹   ENSP00000439276
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,721,833 - 32,765,030 (+)Ensembl
RefSeq Acc Id: ENST00000614767   ⟹   ENSP00000483727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,985 - 31,641,769 (+)Ensembl
RefSeq Acc Id: ENST00000631040
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,221,042 - 32,728,077 (+)Ensembl
RefSeq Acc Id: ENST00000650819   ⟹   ENSP00000498946
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,647,117 - 32,762,021 (+)Ensembl
RefSeq Acc Id: ENST00000650856   ⟹   ENSP00000498216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,309 - 32,764,407 (+)Ensembl
RefSeq Acc Id: ENST00000650866   ⟹   ENSP00000499045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,304 - 32,764,402 (+)Ensembl
RefSeq Acc Id: ENST00000650919   ⟹   ENSP00000498811
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,235 - 32,743,253 (+)Ensembl
RefSeq Acc Id: ENST00000650964
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,730 - 32,728,094 (+)Ensembl
RefSeq Acc Id: ENST00000650967   ⟹   ENSP00000498833
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,327 - 32,743,224 (+)Ensembl
RefSeq Acc Id: ENST00000650980   ⟹   ENSP00000498583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,662 - 32,764,519 (+)Ensembl
RefSeq Acc Id: ENST00000651149   ⟹   ENSP00000498375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,304 - 32,728,077 (+)Ensembl
RefSeq Acc Id: ENST00000651175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,730 - 32,728,090 (+)Ensembl
RefSeq Acc Id: ENST00000651333   ⟹   ENSP00000498590
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,647,089 - 32,774,046 (+)Ensembl
RefSeq Acc Id: ENST00000651335   ⟹   ENSP00000499047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,640,659 - 32,855,666 (+)Ensembl
RefSeq Acc Id: ENST00000651696   ⟹   ENSP00000498690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,647,962 - 32,767,654 (+)Ensembl
RefSeq Acc Id: ENST00000651807
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,290 - 32,728,623 (+)Ensembl
RefSeq Acc Id: ENST00000652588   ⟹   ENSP00000498367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,548,590 - 32,760,813 (+)Ensembl
RefSeq Acc Id: ENST00000652592   ⟹   ENSP00000498646
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl832,646,967 - 32,767,894 (+)Ensembl
RefSeq Acc Id: ENST00000652698   ⟹   ENSP00000499008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl831,639,245 - 32,774,046 (+)Ensembl
RefSeq Acc Id: NM_001159995   ⟹   NP_001153467
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1831,698,194 - 32,827,151 (+)NCBI
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001159996   ⟹   NP_001153468
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,721,835 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,780,921 - 32,827,151 (+)NCBI
T2T-CHM13v2.0833,003,141 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001159999   ⟹   NP_001153471
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1831,698,194 - 32,827,151 (+)NCBI
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160001   ⟹   NP_001153473
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1831,698,194 - 32,827,151 (+)NCBI
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160002   ⟹   NP_001153474
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,728,623 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,787,791 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,009,934 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160004   ⟹   NP_001153476
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160005   ⟹   NP_001153477
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,743,225 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,802,444 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,024,541 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160007   ⟹   NP_001153479
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,728,623 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,787,791 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,009,934 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001160008   ⟹   NP_001153480
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,762,021 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,820,180 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,043,375 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322197   ⟹   NP_001309126
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,721,835 - 32,774,046 (+)NCBI
CHM1_1832,780,921 - 32,827,151 (+)NCBI
T2T-CHM13v2.0833,003,141 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322201   ⟹   NP_001309130
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 32,774,046 (+)NCBI
CHM1_1831,698,194 - 32,827,151 (+)NCBI
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322202   ⟹   NP_001309131
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 32,774,046 (+)NCBI
CHM1_1831,698,194 - 32,827,151 (+)NCBI
T2T-CHM13v2.0831,920,455 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322205   ⟹   NP_001309134
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,647,089 - 32,774,046 (+)NCBI
CHM1_1832,705,907 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,928,406 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322206   ⟹   NP_001309135
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,647,089 - 32,774,046 (+)NCBI
CHM1_1832,705,907 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,928,406 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322207   ⟹   NP_001309136
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,647,089 - 32,762,021 (+)NCBI
CHM1_1832,705,907 - 32,820,180 (+)NCBI
T2T-CHM13v2.0832,928,406 - 33,043,375 (+)NCBI
Sequence:
RefSeq Acc Id: NM_004495   ⟹   NP_004486
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,728,623 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,705,683 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,787,791 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,009,934 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013956   ⟹   NP_039250
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,741,615 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013957   ⟹   NP_039251
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,741,615 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013958   ⟹   NP_039252
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,743,225 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,720,313 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,802,444 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,024,541 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013959   ⟹   NP_039253
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,647,089 - 32,743,225 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,624,071 - 32,720,313 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,705,907 - 32,802,444 (+)NCBI
T2T-CHM13v2.0832,928,406 - 33,024,541 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013960   ⟹   NP_039254
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,741,615 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013962   ⟹   NP_039256
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,545 - 32,743,225 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36831,616,810 - 32,720,313 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1831,698,724 - 32,802,444 (+)NCBI
T2T-CHM13v2.0831,920,755 - 33,024,541 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013964   ⟹   NP_039258
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
GRCh37831,496,820 - 32,622,558 (+)ENTREZGENE
Build 36832,525,295 - 32,741,615 (+)NCBI Archive
HuRef830,042,037 - 31,167,972 (+)ENTREZGENE
CHM1_1832,607,375 - 32,827,151 (+)NCBI
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011544512   ⟹   XP_011542814
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,545 - 32,774,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017013367   ⟹   XP_016868856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,545 - 32,774,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017013368   ⟹   XP_016868857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,774,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017013371   ⟹   XP_016868860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,545 - 32,763,357 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017013372   ⟹   XP_016868861
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,545 - 32,763,357 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054360388   ⟹   XP_054216363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0831,920,755 - 33,055,399 (+)NCBI
RefSeq Acc Id: XM_054360389   ⟹   XP_054216364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0831,920,755 - 33,055,399 (+)NCBI
RefSeq Acc Id: XM_054360390   ⟹   XP_054216365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0832,829,620 - 33,055,399 (+)NCBI
RefSeq Acc Id: XM_054360391   ⟹   XP_054216366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0831,920,755 - 33,044,712 (+)NCBI
RefSeq Acc Id: XM_054360392   ⟹   XP_054216367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0831,920,755 - 33,044,712 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001153467 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153468 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153471 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153473 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153474 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153476 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153477 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153479 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153480 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309126 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309130 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309131 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309134 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309135 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309136 (Get FASTA)   NCBI Sequence Viewer  
  NP_004486 (Get FASTA)   NCBI Sequence Viewer  
  NP_039250 (Get FASTA)   NCBI Sequence Viewer  
  NP_039251 (Get FASTA)   NCBI Sequence Viewer  
  NP_039252 (Get FASTA)   NCBI Sequence Viewer  
  NP_039253 (Get FASTA)   NCBI Sequence Viewer  
  NP_039254 (Get FASTA)   NCBI Sequence Viewer  
  NP_039256 (Get FASTA)   NCBI Sequence Viewer  
  NP_039258 (Get FASTA)   NCBI Sequence Viewer  
  XP_011542814 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868856 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868857 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868860 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868861 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216363 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216364 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216365 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216366 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216367 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA19950 (Get FASTA)   NCBI Sequence Viewer  
  AAA19951 (Get FASTA)   NCBI Sequence Viewer  
  AAA19952 (Get FASTA)   NCBI Sequence Viewer  
  AAA19953 (Get FASTA)   NCBI Sequence Viewer  
  AAA19954 (Get FASTA)   NCBI Sequence Viewer  
  AAA19955 (Get FASTA)   NCBI Sequence Viewer  
  AAA58638 (Get FASTA)   NCBI Sequence Viewer  
  AAA58639 (Get FASTA)   NCBI Sequence Viewer  
  AAA58640 (Get FASTA)   NCBI Sequence Viewer  
  AAA58641 (Get FASTA)   NCBI Sequence Viewer  
  AAB59358 (Get FASTA)   NCBI Sequence Viewer  
  AAB59622 (Get FASTA)   NCBI Sequence Viewer  
  AAC41764 (Get FASTA)   NCBI Sequence Viewer  
  AAD01795 (Get FASTA)   NCBI Sequence Viewer  
  AAH06492 (Get FASTA)   NCBI Sequence Viewer  
  AAH07675 (Get FASTA)   NCBI Sequence Viewer  
  AAH64587 (Get FASTA)   NCBI Sequence Viewer  
  AAH73871 (Get FASTA)   NCBI Sequence Viewer  
  AAI50610 (Get FASTA)   NCBI Sequence Viewer  
  AAM71137 (Get FASTA)   NCBI Sequence Viewer  
  AAM71139 (Get FASTA)   NCBI Sequence Viewer  
  AAM71140 (Get FASTA)   NCBI Sequence Viewer  
  AAO49724 (Get FASTA)   NCBI Sequence Viewer  
  AAP36053 (Get FASTA)   NCBI Sequence Viewer  
  AAQ13665 (Get FASTA)   NCBI Sequence Viewer  
  ABQ53539 (Get FASTA)   NCBI Sequence Viewer  
  ABQ53540 (Get FASTA)   NCBI Sequence Viewer  
  ABQ53541 (Get FASTA)   NCBI Sequence Viewer  
  ABQ53542 (Get FASTA)   NCBI Sequence Viewer  
  ABQ53543 (Get FASTA)   NCBI Sequence Viewer  
  ABR13842 (Get FASTA)   NCBI Sequence Viewer  
  ABR13843 (Get FASTA)   NCBI Sequence Viewer  
  ABR13844 (Get FASTA)   NCBI Sequence Viewer  
  ABY66348 (Get FASTA)   NCBI Sequence Viewer  
  ABY66349 (Get FASTA)   NCBI Sequence Viewer  
  ABY66350 (Get FASTA)   NCBI Sequence Viewer  
  ABY70644 (Get FASTA)   NCBI Sequence Viewer  
  ADN85612 (Get FASTA)   NCBI Sequence Viewer  
  ADN85613 (Get FASTA)   NCBI Sequence Viewer  
  BAD97155 (Get FASTA)   NCBI Sequence Viewer  
  BAF82616 (Get FASTA)   NCBI Sequence Viewer  
  BAF83419 (Get FASTA)   NCBI Sequence Viewer  
  BAG70145 (Get FASTA)   NCBI Sequence Viewer  
  BAG70289 (Get FASTA)   NCBI Sequence Viewer  
  BAH11473 (Get FASTA)   NCBI Sequence Viewer  
  BAH11479 (Get FASTA)   NCBI Sequence Viewer  
  BAH12729 (Get FASTA)   NCBI Sequence Viewer  
  CAG29284 (Get FASTA)   NCBI Sequence Viewer  
  DAA00040 (Get FASTA)   NCBI Sequence Viewer  
  DAA00041 (Get FASTA)   NCBI Sequence Viewer  
  DAA00042 (Get FASTA)   NCBI Sequence Viewer  
  DAA00043 (Get FASTA)   NCBI Sequence Viewer  
  DAA00044 (Get FASTA)   NCBI Sequence Viewer  
  DAA00045 (Get FASTA)   NCBI Sequence Viewer  
  DAA00046 (Get FASTA)   NCBI Sequence Viewer  
  DAA00047 (Get FASTA)   NCBI Sequence Viewer  
  DAA00048 (Get FASTA)   NCBI Sequence Viewer  
  EAW63407 (Get FASTA)   NCBI Sequence Viewer  
  EAW63408 (Get FASTA)   NCBI Sequence Viewer  
  EAW63409 (Get FASTA)   NCBI Sequence Viewer  
  EAW63410 (Get FASTA)   NCBI Sequence Viewer  
  EAW63411 (Get FASTA)   NCBI Sequence Viewer  
  EAW63412 (Get FASTA)   NCBI Sequence Viewer  
  EAW63413 (Get FASTA)   NCBI Sequence Viewer  
  EAW63414 (Get FASTA)   NCBI Sequence Viewer  
  EAW63415 (Get FASTA)   NCBI Sequence Viewer  
  EAW63416 (Get FASTA)   NCBI Sequence Viewer  
  EAW63417 (Get FASTA)   NCBI Sequence Viewer  
  EAW63418 (Get FASTA)   NCBI Sequence Viewer  
  EAW63419 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000287842
  ENSP00000287842.4
  ENSP00000349275
  ENSP00000349275.6
  ENSP00000384620
  ENSP00000384620.2
  ENSP00000428411.1
  ENSP00000428546.1
  ENSP00000428828
  ENSP00000428828.1
  ENSP00000429067
  ENSP00000429067.1
  ENSP00000429582
  ENSP00000429582.1
  ENSP00000430120
  ENSP00000430120.1
  ENSP00000430862
  ENSP00000430862.2
  ENSP00000432052.1
  ENSP00000433289
  ENSP00000433289.1
  ENSP00000433350.2
  ENSP00000434640
  ENSP00000434640.1
  ENSP00000498216.1
  ENSP00000498367.1
  ENSP00000498375.1
  ENSP00000498583
  ENSP00000498583.1
  ENSP00000498590
  ENSP00000498590.1
  ENSP00000498646
  ENSP00000498646.1
  ENSP00000498690.1
  ENSP00000498811
  ENSP00000498811.1
  ENSP00000498833
  ENSP00000498833.1
  ENSP00000498946
  ENSP00000498946.1
  ENSP00000499008
  ENSP00000499008.1
  ENSP00000499045
  ENSP00000499045.1
  ENSP00000499047.1
  ENSP00000500194.1
GenBank Protein Q02297 (Get FASTA)   NCBI Sequence Viewer  
  WDR17091 (Get FASTA)   NCBI Sequence Viewer  
  WDR17092 (Get FASTA)   NCBI Sequence Viewer  
  WDR17093 (Get FASTA)   NCBI Sequence Viewer  
  WDR17094 (Get FASTA)   NCBI Sequence Viewer  
  WDR17095 (Get FASTA)   NCBI Sequence Viewer  
  WDR17096 (Get FASTA)   NCBI Sequence Viewer  
  WDR17097 (Get FASTA)   NCBI Sequence Viewer  
  WDR17098 (Get FASTA)   NCBI Sequence Viewer  
  WDR17099 (Get FASTA)   NCBI Sequence Viewer  
  WDR17100 (Get FASTA)   NCBI Sequence Viewer  
  WDR17101 (Get FASTA)   NCBI Sequence Viewer  
  WDR17102 (Get FASTA)   NCBI Sequence Viewer  
  WDR17103 (Get FASTA)   NCBI Sequence Viewer  
  WDR17104 (Get FASTA)   NCBI Sequence Viewer  
  WDR17105 (Get FASTA)   NCBI Sequence Viewer  
  WDR17106 (Get FASTA)   NCBI Sequence Viewer  
  WDR17107 (Get FASTA)   NCBI Sequence Viewer  
  WDR17108 (Get FASTA)   NCBI Sequence Viewer  
  WDR17109 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001153471   ⟸   NM_001159999
- Peptide Label: isoform HRG-beta1b
- UniProtKB: E3SFM9 (UniProtKB/TrEMBL),   A0A494C1F5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153467   ⟸   NM_001159995
- Peptide Label: isoform HRG-beta1c
- UniProtKB: E3SFM9 (UniProtKB/TrEMBL),   A0A494C1F8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153473   ⟸   NM_001160001
- Peptide Label: isoform HRG-beta1d
- UniProtKB: E3SFM9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039256   ⟸   NM_013962
- Peptide Label: isoform GGF2 precursor
- UniProtKB: Q02297 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_039254   ⟸   NM_013960
- Peptide Label: isoform ndf43 proprotein
- UniProtKB: B0FYA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039258   ⟸   NM_013964
- Peptide Label: isoform HRG-alpha proprotein
- UniProtKB: Q8NFN3 (UniProtKB/Swiss-Prot),   Q8NFN2 (UniProtKB/Swiss-Prot),   Q8NFN1 (UniProtKB/Swiss-Prot),   Q7RTW2 (UniProtKB/Swiss-Prot),   Q7RTW1 (UniProtKB/Swiss-Prot),   Q7RTW0 (UniProtKB/Swiss-Prot),   Q7RTV9 (UniProtKB/Swiss-Prot),   Q15491 (UniProtKB/Swiss-Prot),   Q12784 (UniProtKB/Swiss-Prot),   Q12783 (UniProtKB/Swiss-Prot),   Q12782 (UniProtKB/Swiss-Prot),   Q12781 (UniProtKB/Swiss-Prot),   Q12780 (UniProtKB/Swiss-Prot),   Q12779 (UniProtKB/Swiss-Prot),   Q07111 (UniProtKB/Swiss-Prot),   Q07110 (UniProtKB/Swiss-Prot),   Q02299 (UniProtKB/Swiss-Prot),   Q02298 (UniProtKB/Swiss-Prot),   P98202 (UniProtKB/Swiss-Prot),   O14667 (UniProtKB/Swiss-Prot),   E9PHH4 (UniProtKB/Swiss-Prot),   B7Z4Z3 (UniProtKB/Swiss-Prot),   A8K1L2 (UniProtKB/Swiss-Prot),   A5YAK5 (UniProtKB/Swiss-Prot),   A5YAK4 (UniProtKB/Swiss-Prot),   Q9UPE3 (UniProtKB/Swiss-Prot),   Q02297 (UniProtKB/Swiss-Prot),   Q7RTV8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039250   ⟸   NM_013956
- Peptide Label: isoform HRG-beta1
- UniProtKB: Q7RTW4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153476   ⟸   NM_001160004
- Peptide Label: isoform ndf43b
- UniProtKB: B0FYA9 (UniProtKB/TrEMBL),   A0A494C0K4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039251   ⟸   NM_013957
- Peptide Label: isoform HRG-beta2
- UniProtKB: Q7RTW3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153480   ⟸   NM_001160008
- Peptide Label: isoform HRG-beta2b
- UniProtKB: B0FYA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039252   ⟸   NM_013958
- Peptide Label: isoform HRG-beta3
- UniProtKB: A0A024QY88 (UniProtKB/TrEMBL),   Q6PK61 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153477   ⟸   NM_001160005
- Peptide Label: isoform HRG-beta3b
- UniProtKB: B0FWZ3 (UniProtKB/TrEMBL),   A0A494C114 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_004486   ⟸   NM_004495
- Peptide Label: isoform HRG-gamma
- UniProtKB: Q7RTW5 (UniProtKB/TrEMBL),   B5BU95 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153474   ⟸   NM_001160002
- Peptide Label: isoform HRG-gamma2
- UniProtKB: B0FYA7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153479   ⟸   NM_001160007
- Peptide Label: isoform HRG-gamma3
- UniProtKB: B0FYA8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_039253   ⟸   NM_013959
- Peptide Label: isoform SMDF
- UniProtKB: Q53F54 (UniProtKB/TrEMBL),   Q6ICV5 (UniProtKB/TrEMBL),   Q96IB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153468   ⟸   NM_001159996
- Peptide Label: isoform ndf43c
- UniProtKB: B7Z1D7 (UniProtKB/TrEMBL),   E5RHP6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011542814   ⟸   XM_011544512
- Peptide Label: isoform X1
- UniProtKB: H0YBA3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309130   ⟸   NM_001322201
- Peptide Label: isoform a
- UniProtKB: A5YAK6 (UniProtKB/TrEMBL),   E3SFM9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309131   ⟸   NM_001322202
- Peptide Label: isoform a
- UniProtKB: A5YAK8 (UniProtKB/TrEMBL),   E3SFM9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309135   ⟸   NM_001322206
- Peptide Label: isoform III-2
- UniProtKB: A0A494C0L9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309134   ⟸   NM_001322205
- Peptide Label: isoform NRG-III-beta1a
- UniProtKB: A0A494C0Q4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309136   ⟸   NM_001322207
- Peptide Label: isoform III-3
- UniProtKB: A0A494C1B5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309126   ⟸   NM_001322197
- Peptide Label: isoform VI-1
- UniProtKB: B7Z1E3 (UniProtKB/TrEMBL),   E3SFM9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868860   ⟸   XM_017013371
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016868861   ⟸   XM_017013372
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016868856   ⟸   XM_017013367
- Peptide Label: isoform X2
- UniProtKB: H0YBA3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868857   ⟸   XM_017013368
- Peptide Label: isoform X3
- UniProtKB: Q7RTW4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000428546   ⟸   ENST00000518084
RefSeq Acc Id: ENSP00000432052   ⟸   ENST00000518206
RefSeq Acc Id: ENSP00000429582   ⟸   ENST00000519301
RefSeq Acc Id: ENSP00000428411   ⟸   ENST00000519240
RefSeq Acc Id: ENSP00000498833   ⟸   ENST00000650967
RefSeq Acc Id: ENSP00000498811   ⟸   ENST00000650919
RefSeq Acc Id: ENSP00000498583   ⟸   ENST00000650980
RefSeq Acc Id: ENSP00000498946   ⟸   ENST00000650819
RefSeq Acc Id: ENSP00000498216   ⟸   ENST00000650856
RefSeq Acc Id: ENSP00000499045   ⟸   ENST00000650866
RefSeq Acc Id: ENSP00000498690   ⟸   ENST00000651696
RefSeq Acc Id: ENSP00000498590   ⟸   ENST00000651333
RefSeq Acc Id: ENSP00000499047   ⟸   ENST00000651335
RefSeq Acc Id: ENSP00000498375   ⟸   ENST00000651149
RefSeq Acc Id: ENSP00000434640   ⟸   ENST00000520407
RefSeq Acc Id: ENSP00000499008   ⟸   ENST00000652698
RefSeq Acc Id: ENSP00000498367   ⟸   ENST00000652588
RefSeq Acc Id: ENSP00000498646   ⟸   ENST00000652592
RefSeq Acc Id: ENSP00000433289   ⟸   ENST00000520502
RefSeq Acc Id: ENSP00000483727   ⟸   ENST00000614767
RefSeq Acc Id: ENSP00000428828   ⟸   ENST00000521670
RefSeq Acc Id: ENSP00000500194   ⟸   ENST00000522569
RefSeq Acc Id: ENSP00000430862   ⟸   ENST00000522402
RefSeq Acc Id: ENSP00000384620   ⟸   ENST00000405005
RefSeq Acc Id: ENSP00000429067   ⟸   ENST00000523534
RefSeq Acc Id: ENSP00000287842   ⟸   ENST00000287842
RefSeq Acc Id: ENSP00000433350   ⟸   ENST00000523041
RefSeq Acc Id: ENSP00000430120   ⟸   ENST00000523079
RefSeq Acc Id: ENSP00000439276   ⟸   ENST00000539990
RefSeq Acc Id: ENSP00000349275   ⟸   ENST00000356819
RefSeq Acc Id: XP_054216363   ⟸   XM_054360388
- Peptide Label: isoform X1
- UniProtKB: H0YBA3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054216364   ⟸   XM_054360389
- Peptide Label: isoform X2
- UniProtKB: H0YBA3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054216366   ⟸   XM_054360391
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054216367   ⟸   XM_054360392
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054216365   ⟸   XM_054360390
- Peptide Label: isoform X3
- UniProtKB: Q7RTW4 (UniProtKB/TrEMBL)
Protein Domains
EGF-like   Ig-like   Ig-like C2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q02297-F1-model_v2 AlphaFold Q02297 1-640 view protein structure

Promoters
RGD ID:7213055
Promoter ID:EPDNEW_H12273
Type:initiation region
Name:NRG1_4
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12274  EPDNEW_H12275  EPDNEW_H12276  EPDNEW_H12277  EPDNEW_H12278  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,245 - 31,639,305EPDNEW
RGD ID:7213057
Promoter ID:EPDNEW_H12274
Type:initiation region
Name:NRG1_6
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12275  EPDNEW_H12276  EPDNEW_H12277  EPDNEW_H12278  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,661 - 31,639,721EPDNEW
RGD ID:7213059
Promoter ID:EPDNEW_H12275
Type:initiation region
Name:NRG1_7
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12274  EPDNEW_H12276  EPDNEW_H12277  EPDNEW_H12278  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38831,639,942 - 31,640,002EPDNEW
RGD ID:7213061
Promoter ID:EPDNEW_H12276
Type:initiation region
Name:NRG1_1
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12274  EPDNEW_H12275  EPDNEW_H12277  EPDNEW_H12278  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,311 - 32,548,371EPDNEW
RGD ID:7213063
Promoter ID:EPDNEW_H12277
Type:initiation region
Name:NRG1_3
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12274  EPDNEW_H12275  EPDNEW_H12276  EPDNEW_H12278  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,535 - 32,548,595EPDNEW
RGD ID:7213065
Promoter ID:EPDNEW_H12278
Type:initiation region
Name:NRG1_5
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12274  EPDNEW_H12275  EPDNEW_H12276  EPDNEW_H12277  EPDNEW_H12279  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,548,703 - 32,548,763EPDNEW
RGD ID:7213067
Promoter ID:EPDNEW_H12279
Type:multiple initiation site
Name:NRG1_2
Description:neuregulin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12273  EPDNEW_H12274  EPDNEW_H12275  EPDNEW_H12276  EPDNEW_H12277  EPDNEW_H12278  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38832,647,676 - 32,647,736EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7997 AgrOrtholog
COSMIC NRG1 COSMIC
Ensembl Genes ENSG00000157168 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000287842 ENTREZGENE
  ENST00000287842.7 UniProtKB/Swiss-Prot
  ENST00000356819 ENTREZGENE
  ENST00000356819.7 UniProtKB/Swiss-Prot
  ENST00000405005 ENTREZGENE
  ENST00000405005.8 UniProtKB/Swiss-Prot
  ENST00000518084.5 UniProtKB/TrEMBL
  ENST00000518206.5 UniProtKB/TrEMBL
  ENST00000519240.5 UniProtKB/TrEMBL
  ENST00000519301 ENTREZGENE
  ENST00000519301.6 UniProtKB/Swiss-Prot
  ENST00000520407 ENTREZGENE
  ENST00000520407.5 UniProtKB/Swiss-Prot
  ENST00000520502 ENTREZGENE
  ENST00000520502.7 UniProtKB/Swiss-Prot
  ENST00000521670 ENTREZGENE
  ENST00000521670.5 UniProtKB/Swiss-Prot
  ENST00000522402 ENTREZGENE
  ENST00000522402.6 UniProtKB/TrEMBL
  ENST00000522569.1 UniProtKB/TrEMBL
  ENST00000523041.2 UniProtKB/TrEMBL
  ENST00000523079 ENTREZGENE
  ENST00000523079.5 UniProtKB/Swiss-Prot
  ENST00000523534 ENTREZGENE
  ENST00000523534.5 UniProtKB/TrEMBL
  ENST00000650819 ENTREZGENE
  ENST00000650819.1 UniProtKB/TrEMBL
  ENST00000650856.1 UniProtKB/TrEMBL
  ENST00000650866 ENTREZGENE
  ENST00000650866.1 UniProtKB/TrEMBL
  ENST00000650919 ENTREZGENE
  ENST00000650919.1 UniProtKB/Swiss-Prot
  ENST00000650967 ENTREZGENE
  ENST00000650967.1 UniProtKB/TrEMBL
  ENST00000650980 ENTREZGENE
  ENST00000650980.1 UniProtKB/TrEMBL
  ENST00000651149.1 UniProtKB/TrEMBL
  ENST00000651333 ENTREZGENE
  ENST00000651333.2 UniProtKB/TrEMBL
  ENST00000651335.1 UniProtKB/TrEMBL
  ENST00000651696.1 UniProtKB/TrEMBL
  ENST00000651807 ENTREZGENE
  ENST00000652588.1 UniProtKB/TrEMBL
  ENST00000652592 ENTREZGENE
  ENST00000652592.1 UniProtKB/TrEMBL
  ENST00000652698 ENTREZGENE
  ENST00000652698.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Laminin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000157168 GTEx
HGNC ID HGNC:7997 ENTREZGENE
Human Proteome Map NRG1 Human Proteome Map
InterPro EGF-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuregulin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuregulin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NRG1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:3084 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 3084 ENTREZGENE
OMIM 142445 OMIM
PANTHER PRO-NEUREGULIN-1, MEMBRANE-BOUND ISOFORM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11100 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam EGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuregulin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31776 PharmGKB
PRINTS NEUREGULIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE EGF_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP EGF/Laminin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024QY88 ENTREZGENE, UniProtKB/TrEMBL
  A0A494BZT4_HUMAN UniProtKB/TrEMBL
  A0A494C043_HUMAN UniProtKB/TrEMBL
  A0A494C054_HUMAN UniProtKB/TrEMBL
  A0A494C0K4 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C0L9 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C0Q4 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C0T5_HUMAN UniProtKB/TrEMBL
  A0A494C114 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C1B5 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C1F5 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C1F8 ENTREZGENE, UniProtKB/TrEMBL
  A0A494C1G2_HUMAN UniProtKB/TrEMBL
  A0A5F9ZHA5_HUMAN UniProtKB/TrEMBL
  A5YAK4 ENTREZGENE
  A5YAK5 ENTREZGENE
  A5YAK6 ENTREZGENE, UniProtKB/TrEMBL
  A5YAK7_HUMAN UniProtKB/TrEMBL
  A5YAK8 ENTREZGENE, UniProtKB/TrEMBL
  A6MW54_HUMAN UniProtKB/TrEMBL
  A6MW55_HUMAN UniProtKB/TrEMBL
  A6MW56_HUMAN UniProtKB/TrEMBL
  A8K1L2 ENTREZGENE
  B0FWZ3 ENTREZGENE, UniProtKB/TrEMBL
  B0FYA7 ENTREZGENE, UniProtKB/TrEMBL
  B0FYA8 ENTREZGENE, UniProtKB/TrEMBL
  B0FYA9 ENTREZGENE, UniProtKB/TrEMBL
  B5BU95 ENTREZGENE, UniProtKB/TrEMBL
  B7Z168_HUMAN UniProtKB/TrEMBL
  B7Z1D7 ENTREZGENE, UniProtKB/TrEMBL
  B7Z1E3 ENTREZGENE, UniProtKB/TrEMBL
  B7Z4Z3 ENTREZGENE
  B9EK51_HUMAN UniProtKB/TrEMBL
  E3SFM9 ENTREZGENE, UniProtKB/TrEMBL
  E3SFN0_HUMAN UniProtKB/TrEMBL
  E5RHP6 ENTREZGENE, UniProtKB/TrEMBL
  E5RHQ1_HUMAN UniProtKB/TrEMBL
  E5RIG8_HUMAN UniProtKB/TrEMBL
  E9PHH4 ENTREZGENE
  H0YBA3 ENTREZGENE, UniProtKB/TrEMBL
  H0YCP0_HUMAN UniProtKB/TrEMBL
  H0YDC2_HUMAN UniProtKB/TrEMBL
  NRG1_HUMAN UniProtKB/Swiss-Prot
  O14667 ENTREZGENE
  P98202 ENTREZGENE
  Q02297 ENTREZGENE
  Q02298 ENTREZGENE
  Q02299 ENTREZGENE
  Q07110 ENTREZGENE
  Q07111 ENTREZGENE
  Q12779 ENTREZGENE
  Q12780 ENTREZGENE
  Q12781 ENTREZGENE
  Q12782 ENTREZGENE
  Q12783 ENTREZGENE
  Q12784 ENTREZGENE
  Q15491 ENTREZGENE
  Q53F54 ENTREZGENE, UniProtKB/TrEMBL
  Q6ICV5 ENTREZGENE, UniProtKB/TrEMBL
  Q6PK61 ENTREZGENE, UniProtKB/TrEMBL
  Q7RTV8 ENTREZGENE, UniProtKB/TrEMBL
  Q7RTV9 ENTREZGENE
  Q7RTW0 ENTREZGENE
  Q7RTW1 ENTREZGENE
  Q7RTW2 ENTREZGENE
  Q7RTW3 ENTREZGENE, UniProtKB/TrEMBL
  Q7RTW4 ENTREZGENE, UniProtKB/TrEMBL
  Q7RTW5 ENTREZGENE, UniProtKB/TrEMBL
  Q86WJ0_HUMAN UniProtKB/TrEMBL
  Q8NFN1 ENTREZGENE
  Q8NFN2 ENTREZGENE
  Q8NFN3 ENTREZGENE
  Q96IB3 ENTREZGENE, UniProtKB/TrEMBL
  Q9UPE3 ENTREZGENE
UniProt Secondary A5YAK4 UniProtKB/Swiss-Prot
  A5YAK5 UniProtKB/Swiss-Prot
  A8K1L2 UniProtKB/Swiss-Prot
  B7Z4Z3 UniProtKB/Swiss-Prot
  E9PHH4 UniProtKB/Swiss-Prot
  O14667 UniProtKB/Swiss-Prot
  P98202 UniProtKB/Swiss-Prot
  Q02298 UniProtKB/Swiss-Prot
  Q02299 UniProtKB/Swiss-Prot
  Q07110 UniProtKB/Swiss-Prot
  Q07111 UniProtKB/Swiss-Prot
  Q12779 UniProtKB/Swiss-Prot
  Q12780 UniProtKB/Swiss-Prot
  Q12781 UniProtKB/Swiss-Prot
  Q12782 UniProtKB/Swiss-Prot
  Q12783 UniProtKB/Swiss-Prot
  Q12784 UniProtKB/Swiss-Prot
  Q15491 UniProtKB/Swiss-Prot
  Q7RTV9 UniProtKB/Swiss-Prot
  Q7RTW0 UniProtKB/Swiss-Prot
  Q7RTW1 UniProtKB/Swiss-Prot
  Q7RTW2 UniProtKB/Swiss-Prot
  Q8NFN1 UniProtKB/Swiss-Prot
  Q8NFN2 UniProtKB/Swiss-Prot
  Q8NFN3 UniProtKB/Swiss-Prot
  Q9UPE3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-05 NRG1  neuregulin 1  NRG1-IT2  NRG1 intronic transcript 2 (non-protein coding)  Data merged from RGD:6481115 737654 PROVISIONAL