NR5A2 (nuclear receptor subfamily 5 group A member 2) - Rat Genome Database

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Gene: NR5A2 (nuclear receptor subfamily 5 group A member 2) Homo sapiens
Analyze
Symbol: NR5A2
Name: nuclear receptor subfamily 5 group A member 2
RGD ID: 68499
HGNC Page HGNC:7984
Description: Enables several functions, including nuclear receptor activity; transcription cis-regulatory region binding activity; and transcription coregulator binding activity. Involved in chromatin remodeling; positive regulation of transcription by RNA polymerase II; and positive regulation of viral genome replication. Located in cytoplasm. Is active in nucleus. Biomarker of colon cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: alpha-1-fetoprotein transcription factor; b1-binding factor, hepatocyte transcription factor which activates enhancer II of hepatitis B virus; B1F; B1F2; CPF; CYP7A promoter-binding factor; fetoprotein-alpha 1 (AFP) transcription factor; FTF; FTZ-F1; FTZ-F1beta; hB1F; hB1F-2; hepatocytic transcription factor; hepatocytic transcription factor hB1F-3; liver nuclear receptor homolog-1 variant 2; liver receptor homolog 1; liver receptor homolog-1; LRH-1; LRH1; nuclear receptor NR5A2; nuclear receptor subfamily 5, group A, member 2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381200,027,710 - 200,177,415 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1200,027,614 - 200,177,420 (+)EnsemblGRCh38hg38GRCh38
GRCh371199,996,838 - 200,146,543 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361198,263,393 - 198,413,175 (+)NCBINCBI36Build 36hg18NCBI36
Build 341196,728,426 - 196,878,205NCBI
Celera1173,119,461 - 173,269,192 (+)NCBICelera
Cytogenetic Map1q32.1NCBI
HuRef1171,163,369 - 171,312,952 (+)NCBIHuRef
CHM1_11201,419,353 - 201,569,071 (+)NCBICHM1_1
T2T-CHM13v2.01199,284,725 - 199,434,351 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-demecolcine  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane  (ISO)
1,2-dilauroyl-sn-glycero-3-phosphocholine(1+)  (ISO)
1-O-oleoyl-sn-glycero-3-phosphocholine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 3-benzoate  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-methoxyethanol  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
5-fluorouracil  (ISO)
9-cis-retinoic acid  (EXP)
acetic acid  (ISO)
aflatoxin B1  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
androst-4-ene-3,17-dione  (ISO)
arachidonic acid  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
atrazine  (EXP)
Azoxymethane  (ISO)
aztreonam  (ISO)
benzo[a]pyrene  (EXP)
benzo[e]pyrene  (EXP)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
bromochloroacetic acid  (ISO)
bromocriptine  (ISO)
C60 fullerene  (ISO)
cadmium atom  (EXP)
carbon nanotube  (ISO)
cefalotin  (ISO)
cholesterol  (ISO)
choline  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
cobalt dichloride  (EXP,ISO)
colforsin daropate hydrochloride  (EXP)
crocidolite asbestos  (EXP)
cyclosporin A  (EXP)
dexamethasone  (ISO)
dextran sulfate  (ISO)
dibenz[a,h]anthracene  (ISO)
diethylstilbestrol  (ISO)
Diosbulbin B  (ISO)
dioxygen  (ISO)
endosulfan  (ISO)
flutamide  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
fulvestrant  (EXP)
genistein  (ISO)
gentamycin  (ISO)
imipenem hydrate  (ISO)
L-methionine  (ISO)
lead nitrate  (ISO)
linoleic acid  (ISO)
lipopolysaccharide  (EXP)
lithocholic acid  (ISO)
lysophosphatidylcholine  (ISO)
lysophosphatidylethanolamine  (ISO)
methapyrilene  (EXP,ISO)
methylmercury chloride  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
N-nitrosodiethylamine  (ISO)
neomycin  (ISO)
nitrofen  (ISO)
obeticholic acid  (EXP)
ozone  (ISO)
p-toluidine  (ISO)
paracetamol  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
phorbol 13-acetate 12-myristate  (EXP)
phosphatidylcholine  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (ISO)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
sodium arsenite  (EXP)
succimer  (ISO)
sulforaphane  (ISO)
sulpiride  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
ursodeoxycholic acid  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)
vincristine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
acinar cell differentiation  (IEA)
bile acid metabolic process  (IDA,IEA,ISO)
calcineurin-mediated signaling  (IEA,ISO)
cartilage development  (IEA)
cellular response to leukemia inhibitory factor  (IEA)
cholesterol homeostasis  (IEA)
chromatin remodeling  (IDA,IEA)
embryo development ending in birth or egg hatching  (TAS)
embryonic cleavage  (IEA,ISS)
exocrine pancreas development  (IEA,ISS)
homeostatic process  (NAS)
hormone-mediated signaling pathway  (IBA)
inner cell mass cell differentiation  (IEA,ISS)
intracellular receptor signaling pathway  (IEA)
morula formation  (IEA,ISS)
negative regulation of chondrocyte differentiation  (IEA,ISS)
negative regulation of inflammatory response  (IEA,ISS)
neurogenesis  (IEA,ISS)
pancreas morphogenesis  (IEA)
positive regulation of DNA-templated transcription  (IDA,IEA)
positive regulation of glucocorticoid biosynthetic process  (IEA,ISS)
positive regulation of stem cell differentiation  (IEA,ISS)
positive regulation of T cell activation  (IEA,ISS)
positive regulation of T cell anergy  (IEA,ISS)
positive regulation of T cell proliferation  (IEA,ISS)
positive regulation of tendon cell differentiation  (IEA,ISS)
positive regulation of transcription by RNA polymerase II  (IDA,IEA,ISO,ISS)
positive regulation of viral genome replication  (IDA)
primary ovarian follicle growth  (IEA,ISS)
regulation of cell population proliferation  (IEA)
regulation of DNA-templated transcription  (IDA,IEA,TAS)
regulation of transcription by RNA polymerase II  (IBA)
Sertoli cell development  (IEA,ISS)
somatic stem cell population maintenance  (IEA,ISS)
spermatogenesis  (IEA,ISS)
tissue development  (IBA)
zygotic genome activation  (IEA,ISS)

Cellular Component

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. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Liver receptor homolog-1 (NR5a2) regulates CD95/Fas ligand transcription and associated T-cell effector functions. Schwaderer J, etal., Cell Death Dis. 2017 Apr 13;8(4):e2745. doi: 10.1038/cddis.2017.173.
6. MicroRNA-136 inhibits colon cancer cell proliferation and invasion through targeting liver receptor homolog-1/Wnt signaling. Yuan Q, etal., Gene. 2017 Sep 10;628:48-55. doi: 10.1016/j.gene.2017.07.031. Epub 2017 Jul 12.
Additional References at PubMed
PMID:7680097   PMID:8938589   PMID:9786908   PMID:9858833   PMID:10359768   PMID:11030332   PMID:11564608   PMID:11595170   PMID:11668176   PMID:11927588   PMID:12040021   PMID:12198243  
PMID:12208674   PMID:12477932   PMID:12820970   PMID:12852843   PMID:12853459   PMID:12972592   PMID:14671206   PMID:14701856   PMID:14728801   PMID:14963109   PMID:15117876   PMID:15121760  
PMID:15143151   PMID:15143342   PMID:15181096   PMID:15205472   PMID:15218078   PMID:15327767   PMID:15331348   PMID:15604093   PMID:15613430   PMID:15707893   PMID:15723037   PMID:15897460  
PMID:15923626   PMID:15963945   PMID:16091743   PMID:16271724   PMID:16282330   PMID:16289203   PMID:16439367   PMID:16450584   PMID:16469397   PMID:16712791   PMID:17036045   PMID:17095585  
PMID:17283069   PMID:17522048   PMID:17664281   PMID:17895379   PMID:17910058   PMID:17952562   PMID:17977826   PMID:18029348   PMID:18191017   PMID:18270374   PMID:18385139   PMID:18410128  
PMID:18508634   PMID:18665078   PMID:19015525   PMID:19022561   PMID:19264593   PMID:19274049   PMID:19359379   PMID:19629617   PMID:19692572   PMID:19913121   PMID:20101243   PMID:20133449  
PMID:20159957   PMID:20375098   PMID:20379614   PMID:20516075   PMID:20607599   PMID:20628086   PMID:20817789   PMID:21129436   PMID:21258413   PMID:21262773   PMID:21294900   PMID:21392518  
PMID:21536586   PMID:21554248   PMID:21566081   PMID:21614002   PMID:21873635   PMID:21949357   PMID:21990348   PMID:22048972   PMID:22125638   PMID:22187462   PMID:22359603   PMID:22504882  
PMID:23000165   PMID:23038264   PMID:23128233   PMID:23471216   PMID:23537609   PMID:23637637   PMID:23667258   PMID:23737522   PMID:23817023   PMID:23975195   PMID:24520076   PMID:24564400  
PMID:24570488   PMID:24769073   PMID:25086665   PMID:25223786   PMID:25231870   PMID:25435372   PMID:25514243   PMID:25675535   PMID:25869073   PMID:25873311   PMID:25896302   PMID:25943101  
PMID:25951367   PMID:25987835   PMID:26241054   PMID:26241668   PMID:26268559   PMID:26320367   PMID:26398198   PMID:26400164   PMID:26416531   PMID:26421305   PMID:26530052   PMID:26553876  
PMID:26592175   PMID:26653140   PMID:26677080   PMID:26761123   PMID:27049310   PMID:27298334   PMID:27486225   PMID:27586588   PMID:27694446   PMID:27809310   PMID:27983934   PMID:27984042  
PMID:27996162   PMID:28081303   PMID:28363985   PMID:28440426   PMID:28473536   PMID:28531169   PMID:28642062   PMID:29128635   PMID:29237721   PMID:29438990   PMID:29443959   PMID:29515023  
PMID:29545602   PMID:29669824   PMID:30044146   PMID:30273983   PMID:30305617   PMID:30320362   PMID:30638865   PMID:30740909   PMID:30923324   PMID:31058195   PMID:31328159   PMID:31343991  
PMID:32037723   PMID:32296183   PMID:32433991   PMID:32572717   PMID:32694731   PMID:32931651   PMID:33079429   PMID:33252195   PMID:33335203   PMID:33845483   PMID:34129175   PMID:34310734  
PMID:34561301   PMID:34643922   PMID:35801407   PMID:36217030   PMID:36303447   PMID:36765131   PMID:37204028   PMID:37285077   PMID:38243114   PMID:38409506  


Genomics

Comparative Map Data
NR5A2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381200,027,710 - 200,177,415 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1200,027,614 - 200,177,420 (+)EnsemblGRCh38hg38GRCh38
GRCh371199,996,838 - 200,146,543 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361198,263,393 - 198,413,175 (+)NCBINCBI36Build 36hg18NCBI36
Build 341196,728,426 - 196,878,205NCBI
Celera1173,119,461 - 173,269,192 (+)NCBICelera
Cytogenetic Map1q32.1NCBI
HuRef1171,163,369 - 171,312,952 (+)NCBIHuRef
CHM1_11201,419,353 - 201,569,071 (+)NCBICHM1_1
T2T-CHM13v2.01199,284,725 - 199,434,351 (+)NCBIT2T-CHM13v2.0
Nr5a2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391136,770,300 - 136,888,186 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1136,770,309 - 136,888,186 (-)EnsemblGRCm39 Ensembl
GRCm381136,842,562 - 136,960,448 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1136,842,571 - 136,960,448 (-)EnsemblGRCm38mm10GRCm38
MGSCv371138,740,161 - 138,857,025 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361138,660,687 - 138,776,859 (-)NCBIMGSCv36mm8
Celera1139,488,247 - 139,612,651 (-)NCBICelera
Cytogenetic Map1E4NCBI
cM Map159.98NCBI
Nr5a2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81350,865,253 - 50,985,107 (-)NCBIGRCr8
mRatBN7.21348,313,634 - 48,433,494 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1348,316,301 - 48,433,326 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1350,924,322 - 51,041,371 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01352,212,210 - 52,329,237 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01349,479,256 - 49,596,284 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01353,750,470 - 53,870,288 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1353,750,473 - 53,870,428 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01358,791,496 - 58,910,967 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41349,931,592 - 50,048,756 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11349,945,671 - 50,062,836 (-)NCBI
Celera1348,623,262 - 48,740,634 (-)NCBICelera
Cytogenetic Map13q13NCBI
Nr5a2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540636,263,184 - 36,415,525 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540636,263,257 - 36,415,494 (+)NCBIChiLan1.0ChiLan1.0
NR5A2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2149,206,752 - 49,357,599 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1149,168,065 - 49,318,860 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01175,625,140 - 175,775,955 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11179,934,573 - 180,083,607 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1179,934,573 - 180,083,607 (+)Ensemblpanpan1.1panPan2
NR5A2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.172,925,915 - 3,062,118 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl72,927,326 - 3,062,348 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha72,609,186 - 2,746,673 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.072,572,723 - 2,710,945 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl72,575,836 - 2,711,009 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.172,555,273 - 2,692,729 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.072,656,611 - 2,794,291 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.072,688,192 - 2,825,725 (-)NCBIUU_Cfam_GSD_1.0
Nr5a2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934474,848,490 - 74,960,157 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365674,084,608 - 4,212,854 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365674,084,161 - 4,194,858 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NR5A2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1022,715,735 - 22,865,364 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11022,727,865 - 22,866,905 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21027,281,190 - 27,424,774 (+)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103230356
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12529,230,358 - 29,380,617 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2529,233,558 - 29,379,922 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605530,239,494 - 30,260,729 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nr5a2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624798356,953 - 494,877 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NR5A2
56 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3 copy number gain See cases [RCV000051857] Chr1:187143981..224299417 [GRCh38]
Chr1:187113113..224487119 [GRCh37]
Chr1:185379736..222553742 [NCBI36]
Chr1:1q31.1-42.11
pathogenic
NM_003822.4(NR5A2):c.65-5625G>T single nucleotide variant Lung cancer [RCV000090356] Chr1:200038149 [GRCh38]
Chr1:200007277 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_001276464.1(NR5A2):c.106-735A>T single nucleotide variant Lung cancer [RCV000090357] Chr1:200044708 [GRCh38]
Chr1:200013836 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_001276464.1(NR5A2):c.894+435A>G single nucleotide variant Lung cancer [RCV000090358] Chr1:200049253 [GRCh38]
Chr1:200018381 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_001276464.1(NR5A2):c.894+5256C>G single nucleotide variant Lung cancer [RCV000090359] Chr1:200054074 [GRCh38]
Chr1:200023202 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh38/hg38 1q32.1(chr1:200144603-203112078)x1 copy number loss See cases [RCV000133625] Chr1:200144603..203112078 [GRCh38]
Chr1:200113731..203081206 [GRCh37]
Chr1:198380354..201347829 [NCBI36]
Chr1:1q32.1
pathogenic
NM_205860.3(NR5A2):c.1052A>T (p.Gln351Leu) single nucleotide variant Long QT syndrome [RCV000190193] Chr1:200048760 [GRCh38]
Chr1:200017888 [GRCh37]
Chr1:1q32.1
likely benign
GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3 copy number gain See cases [RCV000240137] Chr1:197811907..228997888 [GRCh37]
Chr1:1q31.3-42.13
pathogenic
NM_205860.3(NR5A2):c.884C>T (p.Thr295Met) single nucleotide variant Anophthalmia-microphthalmia syndrome [RCV000207435] Chr1:200048592 [GRCh38]
Chr1:200017720 [GRCh37]
Chr1:1q32.1
pathogenic|likely benign|uncertain significance
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3 copy number gain See cases [RCV000449172] Chr1:195483439..249213000 [GRCh37]
Chr1:1q31.3-44
pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179413479-201764737)x1 copy number loss See cases [RCV000445748] Chr1:179413479..201764737 [GRCh37]
Chr1:1q25.2-32.1
pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179073386-200192265)x1 copy number loss See cases [RCV000448809] Chr1:179073386..200192265 [GRCh37]
Chr1:1q25.2-32.1
pathogenic
NM_205860.3(NR5A2):c.1230+29_1230+30dup duplication not specified [RCV000455900] Chr1:200111336..200111337 [GRCh38]
Chr1:200080464..200080465 [GRCh37]
Chr1:1q32.1
benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_205860.3(NR5A2):c.905C>A (p.Pro302Gln) single nucleotide variant not specified [RCV004301434] Chr1:200048613 [GRCh38]
Chr1:200017741 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q25.3-41(chr1:185644663-221698833)x3 copy number gain not provided [RCV000749265] Chr1:185644663..221698833 [GRCh37]
Chr1:1q25.3-41
pathogenic
NM_205860.3(NR5A2):c.998G>C (p.Arg333Pro) single nucleotide variant not provided [RCV000969145]|not specified [RCV004029937] Chr1:200048706 [GRCh38]
Chr1:200017834 [GRCh37]
Chr1:1q32.1
benign|likely benign
NM_205860.3(NR5A2):c.464-5A>C single nucleotide variant not provided [RCV000900618] Chr1:200048167 [GRCh38]
Chr1:200017295 [GRCh37]
Chr1:1q32.1
likely benign
NM_205860.3(NR5A2):c.81C>T (p.Asp27=) single nucleotide variant not provided [RCV000917711] Chr1:200039674 [GRCh38]
Chr1:200008802 [GRCh37]
Chr1:1q32.1
likely benign
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44
pathogenic
GRCh37/hg19 1q31.3-32.2(chr1:194356425-210988710)x3 copy number gain not provided [RCV001249273] Chr1:194356425..210988710 [GRCh37]
Chr1:1q31.3-32.2
not provided
GRCh37/hg19 1q31.3-32.1(chr1:196315481-200200856)x1 copy number loss not provided [RCV000847068] Chr1:196315481..200200856 [GRCh37]
Chr1:1q31.3-32.1
uncertain significance
NM_205860.3(NR5A2):c.333G>A (p.Lys111=) single nucleotide variant not provided [RCV000961342] Chr1:200045454 [GRCh38]
Chr1:200014582 [GRCh37]
Chr1:1q32.1
benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance
NM_205860.3(NR5A2):c.681T>G (p.His227Gln) single nucleotide variant Premature ovarian failure [RCV001270190]|not specified [RCV004033449] Chr1:200048389 [GRCh38]
Chr1:200017517 [GRCh37]
Chr1:1q32.1
likely pathogenic|uncertain significance
GRCh37/hg19 1q25.2-32.1(chr1:179073386-200192265) copy number loss not specified [RCV002053769] Chr1:179073386..200192265 [GRCh37]
Chr1:1q25.2-32.1
pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179413479-201764737) copy number loss not specified [RCV002053780] Chr1:179413479..201764737 [GRCh37]
Chr1:1q25.2-32.1
pathogenic
GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3 copy number gain See cases [RCV002287837] Chr1:197867914..249224684 [GRCh37]
Chr1:1q31.3-44
pathogenic
NM_205860.3(NR5A2):c.1321C>T (p.Leu441Phe) single nucleotide variant not specified [RCV004161558] Chr1:200120898 [GRCh38]
Chr1:200090026 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3 copy number gain not provided [RCV002475637] Chr1:181453460..213107248 [GRCh37]
Chr1:1q25.3-32.3
pathogenic
NM_205860.3(NR5A2):c.848C>T (p.Ser283Phe) single nucleotide variant not specified [RCV004198234] Chr1:200048556 [GRCh38]
Chr1:200017684 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1088G>A (p.Ser363Asn) single nucleotide variant not specified [RCV004107708] Chr1:200048796 [GRCh38]
Chr1:200017924 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1304T>C (p.Val435Ala) single nucleotide variant not specified [RCV004112098] Chr1:200120881 [GRCh38]
Chr1:200090009 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1006C>G (p.His336Asp) single nucleotide variant not specified [RCV004142701] Chr1:200048714 [GRCh38]
Chr1:200017842 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.565A>C (p.Asn189His) single nucleotide variant not specified [RCV004103866] Chr1:200048273 [GRCh38]
Chr1:200017401 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.737G>A (p.Ser246Asn) single nucleotide variant not specified [RCV004241737] Chr1:200048445 [GRCh38]
Chr1:200017573 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.770G>T (p.Gly257Val) single nucleotide variant not specified [RCV004184061] Chr1:200048478 [GRCh38]
Chr1:200017606 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.731C>G (p.Pro244Arg) single nucleotide variant not specified [RCV004137607] Chr1:200048439 [GRCh38]
Chr1:200017567 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1598T>C (p.Ile533Thr) single nucleotide variant not specified [RCV004091256] Chr1:200174182 [GRCh38]
Chr1:200143310 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1520G>A (p.Arg507Gln) single nucleotide variant not specified [RCV004192568] Chr1:200174104 [GRCh38]
Chr1:200143232 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.799C>T (p.Arg267Trp) single nucleotide variant not specified [RCV004274186] Chr1:200048507 [GRCh38]
Chr1:200017635 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.196A>G (p.Met66Val) single nucleotide variant not specified [RCV004258869] Chr1:200039789 [GRCh38]
Chr1:200008917 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q32.1(chr1:200101833-200319076)x1 copy number loss not provided [RCV003484011] Chr1:200101833..200319076 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q32.1(chr1:199128985-200237467)x3 copy number gain not provided [RCV003484048] Chr1:199128985..200237467 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q31.3-32.1(chr1:197216705-203683110)x1 copy number loss not specified [RCV003986384] Chr1:197216705..203683110 [GRCh37]
Chr1:1q31.3-32.1
likely pathogenic
GRCh37/hg19 1q32.1(chr1:199373229-204335027)x3 copy number gain not specified [RCV003986684] Chr1:199373229..204335027 [GRCh37]
Chr1:1q32.1
likely pathogenic
NM_205860.3(NR5A2):c.1141T>C (p.Cys381Arg) single nucleotide variant not specified [RCV004491325] Chr1:200111232 [GRCh38]
Chr1:200080360 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1337G>T (p.Arg446Leu) single nucleotide variant not specified [RCV004491326] Chr1:200120914 [GRCh38]
Chr1:200090042 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.756C>G (p.His252Gln) single nucleotide variant not specified [RCV004493396] Chr1:200048464 [GRCh38]
Chr1:200017592 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.998G>A (p.Arg333Gln) single nucleotide variant not specified [RCV004493399] Chr1:200048706 [GRCh38]
Chr1:200017834 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.466G>A (p.Val156Ile) single nucleotide variant not specified [RCV004493395] Chr1:200048174 [GRCh38]
Chr1:200017302 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.793C>G (p.Pro265Ala) single nucleotide variant not specified [RCV004493397] Chr1:200048501 [GRCh38]
Chr1:200017629 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1570G>A (p.Gly524Arg) single nucleotide variant not specified [RCV004491327] Chr1:200174154 [GRCh38]
Chr1:200143282 [GRCh37]
Chr1:1q32.1
uncertain significance
NC_000001.10:g.(?_190829412)_(216061974_?)del deletion not provided [RCV004579260] Chr1:190829412..216061974 [GRCh37]
Chr1:1q31.2-41
pathogenic
NM_205860.3(NR5A2):c.708C>A (p.Asp236Glu) single nucleotide variant not specified [RCV004638676] Chr1:200048416 [GRCh38]
Chr1:200017544 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.896C>T (p.Ala299Val) single nucleotide variant not specified [RCV004638677] Chr1:200048604 [GRCh38]
Chr1:200017732 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1380T>G (p.Asp460Glu) single nucleotide variant not specified [RCV004650406] Chr1:200173964 [GRCh38]
Chr1:200143092 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1505G>A (p.Arg502Gln) single nucleotide variant not specified [RCV004650407] Chr1:200174089 [GRCh38]
Chr1:200143217 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.1568A>G (p.Asn523Ser) single nucleotide variant not specified [RCV004832523] Chr1:200174152 [GRCh38]
Chr1:200143280 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_205860.3(NR5A2):c.743C>G (p.Thr248Arg) single nucleotide variant not specified [RCV004838242] Chr1:200048451 [GRCh38]
Chr1:200017579 [GRCh37]
Chr1:1q32.1
uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:2981
Count of miRNA genes:1158
Interacting mature miRNAs:1470
Transcripts:ENST00000236914, ENST00000367357, ENST00000367362, ENST00000447034, ENST00000474307, ENST00000544748
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597143317GWAS1239391_Hsmoking initiation QTL GWAS1239391 (human)4e-11smoking initiation1200074598200074599Human
597289887GWAS1385961_Hinflammatory bowel disease QTL GWAS1385961 (human)0.0000002inflammatory bowel disease1200108907200108908Human
597262352GWAS1358426_Hhigh density lipoprotein cholesterol measurement QTL GWAS1358426 (human)7e-09high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)1200080174200080175Human
596962717GWAS1082236_Hinflammatory bowel disease, vital capacity QTL GWAS1082236 (human)3e-08inflammatory bowel disease, vital capacity1200115876200115877Human
597052824GWAS1148898_HBMI-adjusted waist-hip ratio QTL GWAS1148898 (human)1e-10body size trait (VT:0100005)1200088375200088376Human
407078860GWAS727836_Hwaist-hip ratio QTL GWAS727836 (human)5e-08waist-hip ratiowaist to hip ratio (WHR) (CMO:0000020)1200067662200067663Human
597067526GWAS1163600_Hpancreatic carcinoma QTL GWAS1163600 (human)8e-16pancreatic carcinoma1200038304200038305Human
597021444GWAS1117518_Hulcerative colitis QTL GWAS1117518 (human)2e-13ulcerative colitis1200132792200132793Human
406980949GWAS629925_Hhematocrit QTL GWAS629925 (human)7e-11hematocrithematocrit (CMO:0000037)1200065841200065842Human
597316749GWAS1412823_Hbody mass index QTL GWAS1412823 (human)0.0000003body mass indexbody mass index (BMI) (CMO:0000105)1200103838200103839Human
596988940GWAS1108459_Hulcerative colitis QTL GWAS1108459 (human)1e-09ulcerative colitis1200132792200132793Human
407024729GWAS673705_Huric acid measurement QTL GWAS673705 (human)0.000007uric acid measurementblood uric acid level (CMO:0000501)1200138297200138298Human
597318150GWAS1414224_Hsmoking initiation QTL GWAS1414224 (human)4e-10smoking initiation1200074598200074599Human
597209348GWAS1305422_Hvital capacity QTL GWAS1305422 (human)8e-09vital capacity1200116586200116587Human
407059551GWAS708527_Hulcerative colitis QTL GWAS708527 (human)2e-17ulcerative colitis1200132792200132793Human
597092490GWAS1188564_Hulcerative colitis QTL GWAS1188564 (human)1e-18ulcerative colitis1200132792200132793Human
597209349GWAS1305423_Hvital capacity QTL GWAS1305423 (human)8e-08vital capacity1200116586200116587Human
597030967GWAS1127041_Hwaist-hip ratio QTL GWAS1127041 (human)1e-10waist-hip ratiowaist to hip ratio (WHR) (CMO:0000020)1200080174200080175Human
597121075GWAS1217149_Hforced expiratory volume QTL GWAS1217149 (human)5e-08forced expiratory volumeforced expiratory volume (CMO:0000254)1200061987200061988Human
597020339GWAS1116413_Hpancreatic carcinoma QTL GWAS1116413 (human)0.000003pancreatic carcinoma1200038304200038305Human
597325104GWAS1421178_Hvital capacity QTL GWAS1421178 (human)2e-14vital capacity1200124759200124760Human
596952890GWAS1072409_Hsize QTL GWAS1072409 (human)2e-09size1200075886200075892Human
406942449GWAS591425_Hforced expiratory volume QTL GWAS591425 (human)3e-08forced expiratory volumeforced expiratory volume (CMO:0000254)1200100088200100089Human
597347112GWAS1443186_Hinflammatory bowel disease QTL GWAS1443186 (human)1e-08inflammatory bowel disease1200115876200115877Human
407073397GWAS722373_HBMI-adjusted waist-hip ratio QTL GWAS722373 (human)3e-14body size trait (VT:0100005)1200067662200067663Human
597316642GWAS1412716_Hbody mass index QTL GWAS1412716 (human)5e-11body mass indexbody mass index (BMI) (CMO:0000105)1200103838200103839Human
406945274GWAS594250_Hhematocrit QTL GWAS594250 (human)3e-12hematocrithematocrit (CMO:0000037)1200064641200064642Human
406948095GWAS597071_Hhemoglobin measurement QTL GWAS597071 (human)1e-12hemoglobin measurementhemoglobin measurement (CMO:0000508)1200064641200064642Human
597166502GWAS1262576_Hopen-angle glaucoma QTL GWAS1262576 (human)1e-09open-angle glaucoma1200077877200077878Human
596977195GWAS1096714_Hulcerative colitis QTL GWAS1096714 (human)3e-12ulcerative colitis1200108907200108908Human
597232605GWAS1328679_Hgut microbiome measurement QTL GWAS1328679 (human)0.0000004gut microbiome measurement1200143875200143876Human
597290716GWAS1386790_Hinflammatory bowel disease, vital capacity QTL GWAS1386790 (human)3e-08inflammatory bowel disease, vital capacity1200115876200115877Human
597230686GWAS1326760_HMyopia QTL GWAS1326760 (human)0.000002Myopia1200079286200079287Human
597051996GWAS1148070_Hintelligence QTL GWAS1148070 (human)0.000002intelligence1200080425200080426Human
597316048GWAS1412122_Hbody mass index QTL GWAS1412122 (human)6e-08body mass indexbody mass index (BMI) (CMO:0000105)1200103838200103839Human
597255634GWAS1351708_Hpancreatic carcinoma QTL GWAS1351708 (human)0.000006pancreatic carcinoma1200047332200047333Human
597051739GWAS1147813_Hhematocrit QTL GWAS1147813 (human)2e-14hematocrithematocrit (CMO:0000037)1200064641200064642Human
407054610GWAS703586_Hvital capacity QTL GWAS703586 (human)7e-12vital capacity1200100088200100089Human
597092930GWAS1189004_Hinflammatory bowel disease QTL GWAS1189004 (human)4e-10inflammatory bowel disease1200132792200132793Human
406985623GWAS634599_Hhemoglobin measurement QTL GWAS634599 (human)1e-09hemoglobin measurementhemoglobin measurement (CMO:0000508)1200065841200065842Human
597161026GWAS1257100_Hlipid measurement QTL GWAS1257100 (human)0.000001lipid measurementblood lipid measurement (CMO:0000050)1200149311200149312Human
407019672GWAS668648_Hpancreatic carcinoma QTL GWAS668648 (human)2e-10pancreatic carcinoma1200038304200038305Human
597287107GWAS1383181_Hulcerative colitis QTL GWAS1383181 (human)3e-12ulcerative colitis1200108907200108908Human
597302208GWAS1398282_Hmonocyte count QTL GWAS1398282 (human)1e-08monocyte quantity (VT:0000223)blood monocyte count (CMO:0000032)1200132305200132306Human
597061581GWAS1157655_Hvital capacity QTL GWAS1157655 (human)5e-15vital capacity1200126807200126808Human
597021006GWAS1117080_Hinflammatory bowel disease QTL GWAS1117080 (human)9e-08inflammatory bowel disease1200132792200132793Human
597059402GWAS1155476_Hadolescent idiopathic scoliosis QTL GWAS1155476 (human)0.0000001adolescent idiopathic scoliosis1200100088200100089Human
597316807GWAS1412881_Hbody mass index QTL GWAS1412881 (human)3e-10body mass indexbody mass index (BMI) (CMO:0000105)1200103838200103839Human
407112229GWAS761205_Hwaist-hip ratio QTL GWAS761205 (human)6e-12waist-hip ratiowaist to hip ratio (WHR) (CMO:0000020)1200088375200088376Human
406954663GWAS603639_Hankylosing spondylitis, psoriasis, ulcerative colitis, Crohn's disease, sclerosing cholangitis QTL GWAS603639 (human)4e-15intestine integrity trait (VT:0010554)1200132792200132793Human
597291377GWAS1387451_Hulcerative colitis QTL GWAS1387451 (human)1e-09ulcerative colitis1200132792200132793Human
597316209GWAS1412283_Hbody mass index QTL GWAS1412283 (human)7e-09body mass indexbody mass index (BMI) (CMO:0000105)1200103838200103839Human
597293033GWAS1389107_Hsize QTL GWAS1389107 (human)2e-09size1200075886200075892Human
597024612GWAS1120686_Hnicotine dependence QTL GWAS1120686 (human)0.000004nicotine dependence1200174314200174315Human
597099364GWAS1195438_Hmonocyte count QTL GWAS1195438 (human)6e-11monocyte quantity (VT:0000223)blood monocyte count (CMO:0000032)1200129879200129880Human
597296365GWAS1392439_Hhematocrit QTL GWAS1392439 (human)4e-09hematocrithematocrit (CMO:0000037)1200088375200088376Human
406946872GWAS595848_Hhemoglobin measurement QTL GWAS595848 (human)4e-11hemoglobin measurementhemoglobin measurement (CMO:0000508)1200064641200064642Human

Markers in Region
D1S2817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,077,172 - 200,077,325UniSTSGRCh37
GRCh37739,236,272 - 39,236,893UniSTSGRCh37
Build 361198,343,795 - 198,343,948RGDNCBI36
Celera739,224,162 - 39,224,783UniSTS
Celera1173,199,882 - 173,200,035RGD
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
HuRef1171,243,624 - 171,243,775UniSTS
HuRef739,120,485 - 39,121,106UniSTS
CRA_TCAGchr7v2739,273,935 - 39,274,556UniSTS
Marshfield Genetic Map1214.08RGD
Marshfield Genetic Map1214.08UniSTS
Genethon Genetic Map1218.2UniSTS
D1S2622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,114,572 - 200,114,752UniSTSGRCh37
Build 361198,381,195 - 198,381,375RGDNCBI36
Celera1173,237,233 - 173,237,405RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,280,990 - 171,281,168UniSTS
Marshfield Genetic Map1214.08UniSTS
Marshfield Genetic Map1214.08RGD
Genethon Genetic Map1218.2UniSTS
TNG Radiation Hybrid Map197676.0UniSTS
deCODE Assembly Map1195.96UniSTS
GeneMap99-GB4 RH Map1663.68UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map11656.8UniSTS
GeneMap99-G3 RH Map17682.0UniSTS
A009V39  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,034,934 - 200,035,066UniSTSGRCh37
Build 361198,301,557 - 198,301,689RGDNCBI36
Celera1173,157,630 - 173,157,762RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,201,598 - 171,201,730UniSTS
GeneMap99-GB4 RH Map1662.05UniSTS
RH94232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,146,193 - 200,146,382UniSTSGRCh37
Build 361198,412,816 - 198,413,005RGDNCBI36
Celera1173,268,834 - 173,269,023RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,312,594 - 171,312,783UniSTS
GeneMap99-GB4 RH Map1665.63UniSTS
RH122291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,122,462 - 200,122,755UniSTSGRCh37
Build 361198,389,085 - 198,389,378RGDNCBI36
Celera1173,245,103 - 173,245,396RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,288,866 - 171,289,159UniSTS
TNG Radiation Hybrid Map197682.0UniSTS
PMC193920P3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371199,995,144 - 199,995,463UniSTSGRCh37
Build 361198,261,767 - 198,262,086RGDNCBI36
Celera1173,117,834 - 173,118,153RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,161,759 - 171,162,078UniSTS
G30215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,146,380 - 200,146,479UniSTSGRCh37
Build 361198,413,003 - 198,413,102RGDNCBI36
Celera1173,269,021 - 173,269,120RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,312,781 - 171,312,880UniSTS
SHGC-76105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,061,598 - 200,061,780UniSTSGRCh37
Build 361198,328,221 - 198,328,403RGDNCBI36
Celera1173,184,305 - 173,184,487RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,228,055 - 171,228,237UniSTS
TNG Radiation Hybrid Map1107684.0UniSTS
GeneMap99-GB4 RH Map1661.94UniSTS
AFM292vd5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,113,319 - 200,113,443UniSTSGRCh37
Build 361198,379,942 - 198,380,066RGDNCBI36
Celera1173,235,988 - 173,236,104RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,279,745 - 171,279,861UniSTS
Whitehead-RH Map1821.5UniSTS
NCBI RH Map11656.9UniSTS
SHGC-76109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,034,840 - 200,034,989UniSTSGRCh37
Build 361198,301,463 - 198,301,612RGDNCBI36
Celera1173,157,536 - 173,157,685RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,201,504 - 171,201,653UniSTS
TNG Radiation Hybrid Map1107690.0UniSTS
GeneMap99-GB4 RH Map1663.78UniSTS
GeneMap99-GB4 RH Map1662.05UniSTS
Whitehead-RH Map1822.0UniSTS
NCBI RH Map11657.5UniSTS
SHGC-76125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,119,602 - 200,119,699UniSTSGRCh37
Build 361198,386,225 - 198,386,322RGDNCBI36
Celera1173,242,243 - 173,242,340RGD
Cytogenetic Map1q32.1UniSTS
HuRef1171,286,006 - 171,286,103UniSTS
TNG Radiation Hybrid Map197682.0UniSTS
GeneMap99-GB4 RH Map1665.89UniSTS
G32891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371200,034,934 - 200,035,066UniSTSGRCh37
Celera1173,157,630 - 173,157,762UniSTS
Cytogenetic Map1q32.1UniSTS
HuRef1171,201,598 - 171,201,730UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2430 2780 2229 4515 1722 2334 4 622 1506 465 2266 6816 6000 50 3282 833 1721 1600 170

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_050913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001276464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_205860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054335752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB019246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB307719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC096633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF049102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF112344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF124247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF124248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF146343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF190464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF228413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF319643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC027893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC118571 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC118652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA776772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB162803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU714233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HQ692857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U80251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U93553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000236914   ⟹   ENSP00000236914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,027,614 - 200,175,603 (+)Ensembl
Ensembl Acc Id: ENST00000367357   ⟹   ENSP00000356326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,043,810 - 200,058,424 (+)Ensembl
Ensembl Acc Id: ENST00000367362   ⟹   ENSP00000356331
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,027,710 - 200,177,415 (+)Ensembl
Ensembl Acc Id: ENST00000447034   ⟹   ENSP00000414888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,027,883 - 200,039,769 (+)Ensembl
Ensembl Acc Id: ENST00000474307   ⟹   ENSP00000436776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,027,657 - 200,044,535 (+)Ensembl
Ensembl Acc Id: ENST00000544748   ⟹   ENSP00000439116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1200,042,825 - 200,177,420 (+)Ensembl
RefSeq Acc Id: NM_001276464   ⟹   NP_001263393
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,042,591 - 200,177,415 (+)NCBI
GRCh371199,996,730 - 200,146,552 (+)NCBI
HuRef1171,163,369 - 171,312,952 (+)NCBI
CHM1_11201,434,569 - 201,569,071 (+)NCBI
T2T-CHM13v2.01199,299,606 - 199,434,351 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003822   ⟹   NP_003813
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,027,710 - 200,177,415 (+)NCBI
GRCh371199,996,730 - 200,146,552 (+)NCBI
Build 361198,263,393 - 198,413,175 (+)NCBI Archive
HuRef1171,163,369 - 171,312,952 (+)NCBI
CHM1_11201,419,353 - 201,569,071 (+)NCBI
T2T-CHM13v2.01199,284,725 - 199,434,351 (+)NCBI
Sequence:
RefSeq Acc Id: NM_205860   ⟹   NP_995582
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,027,710 - 200,177,415 (+)NCBI
Build 361198,263,393 - 198,413,175 (+)NCBI Archive
HuRef1171,163,369 - 171,312,952 (+)NCBI
CHM1_11201,419,353 - 201,569,071 (+)NCBI
T2T-CHM13v2.01199,284,725 - 199,434,351 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245062   ⟹   XP_005245119
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,042,591 - 200,177,415 (+)NCBI
GRCh371199,996,730 - 200,146,552 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509381   ⟹   XP_011507683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,037,025 - 200,177,415 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509384   ⟹   XP_011507686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,038,936 - 200,177,415 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000904   ⟹   XP_016856393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,038,936 - 200,177,415 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047416753   ⟹   XP_047272709
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,035,030 - 200,177,415 (+)NCBI
RefSeq Acc Id: XM_047416762   ⟹   XP_047272718
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,039,617 - 200,177,415 (+)NCBI
RefSeq Acc Id: XM_054335749   ⟹   XP_054191724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01199,295,917 - 199,434,351 (+)NCBI
RefSeq Acc Id: XM_054335750   ⟹   XP_054191725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01199,294,040 - 199,434,351 (+)NCBI
RefSeq Acc Id: XM_054335751   ⟹   XP_054191726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01199,299,404 - 199,434,351 (+)NCBI
RefSeq Acc Id: XM_054335752   ⟹   XP_054191727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01199,295,933 - 199,434,351 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001263393 (Get FASTA)   NCBI Sequence Viewer  
  NP_003813 (Get FASTA)   NCBI Sequence Viewer  
  NP_995582 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245119 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507683 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507686 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856393 (Get FASTA)   NCBI Sequence Viewer  
  XP_047272709 (Get FASTA)   NCBI Sequence Viewer  
  XP_047272718 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191724 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191725 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191726 (Get FASTA)   NCBI Sequence Viewer  
  XP_054191727 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC78727 (Get FASTA)   NCBI Sequence Viewer  
  AAD03155 (Get FASTA)   NCBI Sequence Viewer  
  AAD03248 (Get FASTA)   NCBI Sequence Viewer  
  AAD26565 (Get FASTA)   NCBI Sequence Viewer  
  AAD26566 (Get FASTA)   NCBI Sequence Viewer  
  AAD37378 (Get FASTA)   NCBI Sequence Viewer  
  AAG17124 (Get FASTA)   NCBI Sequence Viewer  
  AAG17125 (Get FASTA)   NCBI Sequence Viewer  
  AAI18572 (Get FASTA)   NCBI Sequence Viewer  
  AAI18653 (Get FASTA)   NCBI Sequence Viewer  
  AAL37171 (Get FASTA)   NCBI Sequence Viewer  
  ACD87739 (Get FASTA)   NCBI Sequence Viewer  
  ADZ17368 (Get FASTA)   NCBI Sequence Viewer  
  BAA34092 (Get FASTA)   NCBI Sequence Viewer  
  BAG65188 (Get FASTA)   NCBI Sequence Viewer  
  BAG65205 (Get FASTA)   NCBI Sequence Viewer  
  BAH02310 (Get FASTA)   NCBI Sequence Viewer  
  BAH14884 (Get FASTA)   NCBI Sequence Viewer  
  EAW91305 (Get FASTA)   NCBI Sequence Viewer  
  EAW91306 (Get FASTA)   NCBI Sequence Viewer  
  EAW91307 (Get FASTA)   NCBI Sequence Viewer  
  EAW91308 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000236914
  ENSP00000236914.3
  ENSP00000356326.3
  ENSP00000356331
  ENSP00000356331.3
  ENSP00000414888.1
  ENSP00000436776.1
  ENSP00000439116
  ENSP00000439116.1
GenBank Protein O00482 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_995582   ⟸   NM_205860
- Peptide Label: isoform 1
- UniProtKB: O95642 (UniProtKB/Swiss-Prot),   B4E2P3 (UniProtKB/Swiss-Prot),   Q147U3 (UniProtKB/Swiss-Prot),   O00482 (UniProtKB/Swiss-Prot),   Q9UEC0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_003813   ⟸   NM_003822
- Peptide Label: isoform 2
- UniProtKB: F1D8R9 (UniProtKB/TrEMBL),   B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001263393   ⟸   NM_001276464
- Peptide Label: isoform 3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245119   ⟸   XM_005245062
- Peptide Label: isoform X4
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507683   ⟸   XM_011509381
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507686   ⟸   XM_011509384
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856393   ⟸   XM_017000904
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000439116   ⟸   ENST00000544748
Ensembl Acc Id: ENSP00000356331   ⟸   ENST00000367362
Ensembl Acc Id: ENSP00000356326   ⟸   ENST00000367357
Ensembl Acc Id: ENSP00000236914   ⟸   ENST00000236914
Ensembl Acc Id: ENSP00000414888   ⟸   ENST00000447034
Ensembl Acc Id: ENSP00000436776   ⟸   ENST00000474307
RefSeq Acc Id: XP_047272709   ⟸   XM_047416753
- Peptide Label: isoform X1
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047272718   ⟸   XM_047416762
- Peptide Label: isoform X2
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191725   ⟸   XM_054335750
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191724   ⟸   XM_054335749
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191727   ⟸   XM_054335752
- Peptide Label: isoform X3
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054191726   ⟸   XM_054335751
- Peptide Label: isoform X4
- UniProtKB: B4E2M6 (UniProtKB/TrEMBL),   B6ZGU9 (UniProtKB/TrEMBL)
Protein Domains
NR LBD   Nuclear receptor

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O00482-F1-model_v2 AlphaFold O00482 1-541 view protein structure

Promoters
RGD ID:6858506
Promoter ID:EPDNEW_H2418
Type:initiation region
Name:NR5A2_2
Description:nuclear receptor subfamily 5 group A member 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2419  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,027,597 - 200,027,657EPDNEW
RGD ID:6858508
Promoter ID:EPDNEW_H2419
Type:initiation region
Name:NR5A2_1
Description:nuclear receptor subfamily 5 group A member 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2418  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381200,027,710 - 200,027,770EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7984 AgrOrtholog
COSMIC NR5A2 COSMIC
Ensembl Genes ENSG00000116833 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000236914 ENTREZGENE
  ENST00000236914.7 UniProtKB/Swiss-Prot
  ENST00000367357.3 UniProtKB/TrEMBL
  ENST00000367362 ENTREZGENE
  ENST00000367362.8 UniProtKB/Swiss-Prot
  ENST00000447034.1 UniProtKB/TrEMBL
  ENST00000474307.1 UniProtKB/TrEMBL
  ENST00000544748 ENTREZGENE
  ENST00000544748.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.565.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.50.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000116833 GTEx
HGNC ID HGNC:7984 ENTREZGENE
Human Proteome Map NR5A2 Human Proteome Map
InterPro NHR-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NR5_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nucl_hrmn_rcpt_lig-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuclear_hrmn_rcpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_hrmn_rcpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_NHR/GATA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:2494 UniProtKB/Swiss-Prot
NCBI Gene 2494 ENTREZGENE
OMIM 604453 OMIM
PANTHER NUCLEAR RECEPTOR SUBFAMILY 5 GROUP A MEMBER 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR24086 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Hormone_recep UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31765 PharmGKB
PIRSF Nuc_orph_FTZ-F1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS F138DOMAIN UniProtKB/TrEMBL
  STRDHORMONER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STROIDFINGER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE NR_LBD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NUCLEAR_REC_DBD_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NUCLEAR_REC_DBD_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HOLI UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Glucocorticoid receptor-like (DNA-binding domain) UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48508 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B3GPJ3_HUMAN UniProtKB/TrEMBL
  B4E2M6 ENTREZGENE, UniProtKB/TrEMBL
  B4E2P3 ENTREZGENE
  B6ZGU9 ENTREZGENE, UniProtKB/TrEMBL
  E9PQH2_HUMAN UniProtKB/TrEMBL
  F1D8R9 ENTREZGENE, UniProtKB/TrEMBL
  H0Y328_HUMAN UniProtKB/TrEMBL
  H0Y7S7_HUMAN UniProtKB/TrEMBL
  NR5A2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  O95642 ENTREZGENE
  Q147U3 ENTREZGENE
  Q8WY08_HUMAN UniProtKB/TrEMBL
  Q9UEC0 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary B4E2P3 UniProtKB/Swiss-Prot
  O95642 UniProtKB/Swiss-Prot
  Q147U3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 NR5A2  nuclear receptor subfamily 5 group A member 2    nuclear receptor subfamily 5, group A, member 2  Symbol and/or name change 5135510 APPROVED