NCOA3 (nuclear receptor coactivator 3) - Rat Genome Database

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Gene: NCOA3 (nuclear receptor coactivator 3) Homo sapiens
Analyze
Symbol: NCOA3
Name: nuclear receptor coactivator 3
RGD ID: 1344181
HGNC Page HGNC:7670
Description: Enables several functions, including disordered domain specific binding activity; nuclear receptor binding activity; and nuclear receptor coactivator activity. Involved in several processes, including cellular response to estradiol stimulus; nuclear receptor-mediated signaling pathway; and positive regulation of keratinocyte differentiation. Located in chromatin; cytosol; and nucleoplasm. Part of protein-containing complex. Implicated in obesity. Biomarker of breast carcinoma and prostate cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ACTR; AIB-1; AIB1; amplified in breast cancer 1 protein; bHLHe42; CAGH16; CBP-interacting protein; class E basic helix-loop-helix protein 42; CTG26; KAT13B; MGC141848; pCIP; RAC3; receptor-associated coactivator 3; SRC-3; SRC3; steroid receptor coactivator protein 3; thyroid hormone receptor activator molecule 1; TNRC14; TNRC16; TRAM-1
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
NCBI Annotation Information: Note: RAC3 (Gene ID: 5881) and NCOA3 (Gene ID: 8202) share the RAC3 symbol/alias in common. RAC3 is a widely used alternative name for nuclear receptor coactivator 3 (NCOA3), which can be confused with the official symbol for ras-related C3 botulinum toxin substrate 3 (RAC3). [06 Jul 2018]
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382047,501,887 - 47,656,872 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2047,501,887 - 47,656,877 (+)EnsemblGRCh38hg38GRCh38
GRCh372046,130,631 - 46,285,616 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362045,564,064 - 45,719,023 (+)NCBINCBI36Build 36hg18NCBI36
Build 342045,564,063 - 45,719,019NCBI
Celera2042,844,227 - 42,999,274 (+)NCBICelera
Cytogenetic Map20q13.12NCBI
HuRef2042,872,332 - 43,026,949 (+)NCBIHuRef
CHM1_12046,033,477 - 46,188,916 (+)NCBICHM1_1
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-gambogic acid  (EXP)
1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-hydroxy-17-methylestra-4,9,11-trien-3-one  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,4,7,8-Pentachlorodibenzofuran  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (EXP)
6-(4-chlorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime  (EXP)
afimoxifene  (EXP)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP,ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
androst-4-ene-3,17-dione  (EXP)
arsenite(3-)  (EXP)
bazedoxifene  (EXP)
benzamide  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
Benzo[ghi]perylene  (EXP)
benzoates  (EXP)
bis(2-chloroethyl) sulfide  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
bortezomib  (EXP)
butamben  (EXP)
C60 fullerene  (ISO)
cadmium atom  (EXP)
caffeine  (EXP)
calcitriol  (EXP,ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
clemizole  (EXP)
cobalt dichloride  (EXP)
cocaine  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
coumarin  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
cyclosporin A  (EXP)
cyproterone acetate  (EXP)
DDE  (EXP)
deguelin  (EXP)
dexamethasone  (EXP)
Dibutyl phosphate  (EXP)
diclofenac  (EXP)
diethylstilbestrol  (EXP)
dorsomorphin  (EXP)
estrone  (EXP)
flavonol  (EXP)
folic acid  (ISO)
FR900359  (EXP)
fulvestrant  (EXP)
galangin  (EXP)
genistein  (EXP,ISO)
gentamycin  (ISO)
indometacin  (EXP)
kaempferol  (EXP)
leflunomide  (EXP)
melatonin  (EXP)
mercury atom  (EXP)
mercury(0)  (EXP)
methotrexate  (ISO)
methylmercury chloride  (EXP)
mifepristone  (ISO)
Mitotane  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP)
nickel atom  (EXP)
ochratoxin A  (EXP)
oxaliplatin  (ISO)
ozone  (ISO)
paclitaxel  (EXP)
paracetamol  (EXP,ISO)
permethrin  (EXP)
Phenoxybenzamine  (EXP)
phenylmercury acetate  (EXP)
raloxifene  (EXP)
resveratrol  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sunitinib  (EXP)
tamoxifen  (EXP)
temozolomide  (EXP)
testosterone enanthate  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
torcetrapib  (EXP)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (EXP)
troglitazone  (ISO)
tungsten  (ISO)
urethane  (EXP)
valproic acid  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Androgen receptor coregulators and their involvement in the development and progression of prostate cancer. Chmelar R, etal., Int J Cancer. 2007 Feb 15;120(4):719-33.
2. Role of estrogen receptor alpha transcriptional coregulators in tamoxifen resistance in breast cancer. Girault I, etal., Maturitas. 2006 Jul 20;54(4):342-51. Epub 2006 Jul 5.
3. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
4. Coregulators in nuclear estrogen receptor action: from concept to therapeutic targeting. Hall JM and McDonnell DP, Mol Interv. 2005 Dec;5(6):343-57.
5. The Nrf2 regulatory network provides an interface between redox and intermediary metabolism. Hayes JD and Dinkova-Kostova AT, Trends Biochem Sci. 2014 Apr;39(4):199-218. doi: 10.1016/j.tibs.2014.02.002. Epub 2014 Mar 16.
6. Differential regulation of steroid nuclear receptor coregulator expression between normal and neoplastic prostate epithelial cells. Heemers HV, etal., Prostate. 2010 Jun 15;70(9):959-70.
7. Expression of sex steroid receptors and their co-factors in normal and malignant breast tissue: AIB1 is a carcinoma-specific co-activator. Hudelist G, etal., Breast Cancer Res Treat. 2003 Mar;78(2):193-204.
8. Novel glucocorticoid receptor coactivator effector mechanisms. Jenkins BD, etal., Trends Endocrinol Metab. 2001 Apr;12(3):122-6.
9. The human glucocorticoid receptor: molecular basis of biologic function. Nicolaides NC, etal., Steroids. 2010 Jan;75(1):1-12. Epub 2009 Oct 7.
10. Prepubertal genistein exposure affects erbB2/Akt signal and reduces rat mammary tumorigenesis. Peng JH, etal., Eur J Cancer Prev. 2010 Mar;19(2):110-9.
11. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
12. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
13. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
14. Dynamic and combinatorial control of gene expression by nuclear retinoic acid receptors (RARs). Rochette-Egly C and Germain P, Nucl Recept Signal. 2009 May 8;7:e005.
15. Correlates of obesity in postmenopausal women with breast cancer: comparison of genetic, demographic, disease-related, life history and dietary factors. Wasserman L, etal., Int J Obes Relat Metab Disord. 2004 Jan;28(1):49-56.
Additional References at PubMed
PMID:7791754   PMID:8616895   PMID:8758910   PMID:8889548   PMID:9192892   PMID:9225980   PMID:9238002   PMID:9252329   PMID:9267036   PMID:9346901   PMID:9445475   PMID:9489701  
PMID:9727751   PMID:9765300   PMID:9812974   PMID:9832502   PMID:10224118   PMID:10490106   PMID:10504300   PMID:10551785   PMID:10598588   PMID:10652338   PMID:10655477   PMID:10681591  
PMID:10757795   PMID:10777539   PMID:10866661   PMID:10965917   PMID:11027271   PMID:11050077   PMID:11050174   PMID:11056690   PMID:11076796   PMID:11087842   PMID:11092404   PMID:11094166  
PMID:11117530   PMID:11161840   PMID:11163245   PMID:11266503   PMID:11279242   PMID:11316771   PMID:11353774   PMID:11376110   PMID:11389589   PMID:11477071   PMID:11500849   PMID:11668176  
PMID:11704662   PMID:11708882   PMID:11747336   PMID:11780052   PMID:11823864   PMID:11851396   PMID:11877444   PMID:11927493   PMID:11929748   PMID:11971985   PMID:12082103   PMID:12089344  
PMID:12145209   PMID:12477932   PMID:12497632   PMID:12529369   PMID:12554772   PMID:12569362   PMID:12602902   PMID:12630920   PMID:12650696   PMID:12665583   PMID:12714702   PMID:12833450  
PMID:12893883   PMID:12917342   PMID:14503806   PMID:14578343   PMID:14611647   PMID:14645221   PMID:14648706   PMID:14684685   PMID:14691461   PMID:14747462   PMID:14766010   PMID:14966121  
PMID:14966289   PMID:15001550   PMID:15145444   PMID:15145939   PMID:15169882   PMID:15174051   PMID:15184363   PMID:15289619   PMID:15302935   PMID:15383283   PMID:15448000   PMID:15449938  
PMID:15548698   PMID:15550471   PMID:15563469   PMID:15572661   PMID:15604093   PMID:15677324   PMID:15698540   PMID:15723037   PMID:15788656   PMID:15788663   PMID:15808510   PMID:15831516  
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PMID:16298470   PMID:16331275   PMID:16344560   PMID:16365010   PMID:16373399   PMID:16434590   PMID:16439211   PMID:16456540   PMID:16458427   PMID:16648476   PMID:16670003   PMID:16728408  
PMID:16751102   PMID:16760465   PMID:16860316   PMID:16916939   PMID:16921507   PMID:16923966   PMID:16938873   PMID:16940181   PMID:16951183   PMID:16957778   PMID:16964243   PMID:17008696  
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PMID:17646391   PMID:17805331   PMID:17927986   PMID:17968310   PMID:17998543   PMID:18003620   PMID:18029348   PMID:18160712   PMID:18162290   PMID:18246597   PMID:18267973   PMID:18313384  
PMID:18385039   PMID:18426732   PMID:18484708   PMID:18511550   PMID:18521745   PMID:18570454   PMID:18593948   PMID:18593949   PMID:18636124   PMID:18644862   PMID:18645020   PMID:18660489  
PMID:18676680   PMID:18765637   PMID:18798693   PMID:18827493   PMID:18845648   PMID:18922467   PMID:19052561   PMID:19064572   PMID:19095746   PMID:19102007   PMID:19144644   PMID:19170196  
PMID:19176441   PMID:19183483   PMID:19198599   PMID:19198856   PMID:19255064   PMID:19274049   PMID:19277704   PMID:19285025   PMID:19322201   PMID:19357364   PMID:19433130   PMID:19453261  
PMID:19460752   PMID:19462000   PMID:19470168   PMID:19491275   PMID:19552757   PMID:19596656   PMID:19625176   PMID:19628566   PMID:19652917   PMID:19692168   PMID:19716257   PMID:19884766  
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PMID:20956942   PMID:21047772   PMID:21059860   PMID:21182203   PMID:21184786   PMID:21220509   PMID:21454665   PMID:21577200   PMID:21601620   PMID:21632823   PMID:21636853   PMID:21735116  
PMID:21871888   PMID:21873635   PMID:21914189   PMID:22002538   PMID:22035181   PMID:22052107   PMID:22142990   PMID:22147914   PMID:22163316   PMID:22213475   PMID:22283414   PMID:22307791  
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PMID:36574265   PMID:36613751   PMID:36658474   PMID:37689310   PMID:37704626   PMID:38297188   PMID:38360978   PMID:38483947  


Genomics

Comparative Map Data
NCOA3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382047,501,887 - 47,656,872 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2047,501,887 - 47,656,877 (+)EnsemblGRCh38hg38GRCh38
GRCh372046,130,631 - 46,285,616 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362045,564,064 - 45,719,023 (+)NCBINCBI36Build 36hg18NCBI36
Build 342045,564,063 - 45,719,019NCBI
Celera2042,844,227 - 42,999,274 (+)NCBICelera
Cytogenetic Map20q13.12NCBI
HuRef2042,872,332 - 43,026,949 (+)NCBIHuRef
CHM1_12046,033,477 - 46,188,916 (+)NCBICHM1_1
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBIT2T-CHM13v2.0
Ncoa3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392165,834,557 - 165,915,162 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2165,834,545 - 165,915,162 (+)EnsemblGRCm39 Ensembl
GRCm382165,992,637 - 166,073,242 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2165,992,636 - 166,073,242 (+)EnsemblGRCm38mm10GRCm38
MGSCv372165,818,137 - 165,898,742 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362165,726,090 - 165,761,651 (+)NCBIMGSCv36mm8
Celera2171,928,977 - 172,011,677 (+)NCBICelera
Cytogenetic Map2H3NCBI
cM Map286.22NCBI
Ncoa3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83175,157,824 - 175,237,831 (+)NCBIGRCr8
mRatBN7.23154,738,566 - 154,821,395 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3154,738,581 - 154,818,594 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3158,538,937 - 158,619,397 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03167,037,941 - 167,118,397 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03164,779,584 - 164,860,043 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03162,692,176 - 162,788,582 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3162,692,185 - 162,787,548 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03168,863,837 - 168,959,427 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43157,168,492 - 157,196,566 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13157,079,533 - 157,100,362 (+)NCBI
Celera3153,323,587 - 153,406,335 (+)NCBICelera
Cytogenetic Map3q42NCBI
Ncoa3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544510,024,308 - 10,052,472 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495544510,020,916 - 10,085,318 (-)NCBIChiLan1.0ChiLan1.0
NCOA3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22153,240,803 - 53,395,781 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12053,233,900 - 53,388,887 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02043,838,227 - 43,992,407 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12044,919,348 - 45,073,549 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2045,000,422 - 45,073,549 (+)Ensemblpanpan1.1panPan2
NCOA3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl2434,585,305 - 34,728,674 (+)NCBICanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2434,585,305 - 34,728,674 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2434,044,925 - 34,190,239 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02435,293,645 - 35,438,878 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2435,293,662 - 35,438,852 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12434,528,192 - 34,678,477 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02434,667,908 - 34,813,062 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02435,208,068 - 35,353,609 (+)NCBIUU_Cfam_GSD_1.0
Ncoa3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640190,446,492 - 190,514,236 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365145,901,601 - 5,967,865 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365145,900,135 - 5,967,862 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NCOA3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1749,528,179 - 49,663,200 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11749,528,275 - 49,660,471 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21755,850,658 - 55,874,660 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NCOA3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1216,270,218 - 16,423,381 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl216,273,717 - 16,423,318 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605064,808,267 - 64,961,547 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ncoa3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247907,232,519 - 7,358,684 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247907,229,152 - 7,358,627 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NCOA3
51 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 20q13.12-13.33(chr20:44787704-64277321)x3 copy number gain See cases [RCV000053035] Chr20:44787704..64277321 [GRCh38]
Chr20:43416345..62908674 [GRCh37]
Chr20:42849759..62379118 [NCBI36]
Chr20:20q13.12-13.33		 pathogenic
NM_181659.2(NCOA3):c.683C>T (p.Ala228Val) single nucleotide variant Malignant melanoma [RCV000072672] Chr20:47627711 [GRCh38]
Chr20:46256455 [GRCh37]
Chr20:45689862 [NCBI36]
Chr20:20q13.12		 not provided
GRCh38/hg38 20q13.12(chr20:47390946-47514274)x3 copy number gain See cases [RCV000135200] Chr20:47390946..47514274 [GRCh38]
Chr20:46019690..46143018 [GRCh37]
Chr20:45453097..45576425 [NCBI36]
Chr20:20q13.12		 likely benign
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 copy number gain See cases [RCV000135859] Chr20:99557..64277321 [GRCh38]
Chr20:80198..62908674 [GRCh37]
Chr20:28198..62379118 [NCBI36]
Chr20:20p13-q13.33		 pathogenic
GRCh38/hg38 20q11.22-13.12(chr20:35237946-47631818)x1 copy number loss See cases [RCV000140816] Chr20:35237946..47631818 [GRCh38]
Chr20:33825749..46260562 [GRCh37]
Chr20:33289165..45693969 [NCBI36]
Chr20:20q11.22-13.12		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 copy number gain See cases [RCV000510832] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_181659.3(NCOA3):c.3998A>G (p.Asn1333Ser) single nucleotide variant not specified [RCV004301919] Chr20:47652457 [GRCh38]
Chr20:46281201 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.751C>T (p.Arg251Cys) single nucleotide variant not specified [RCV004295137] Chr20:47627951 [GRCh38]
Chr20:46256695 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2032T>G (p.Leu678Val) single nucleotide variant not specified [RCV004300978] Chr20:47636418 [GRCh38]
Chr20:46265162 [GRCh37]
Chr20:20q13.12		 uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) copy number gain See cases [RCV000512450] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 copy number gain not provided [RCV000741058] Chr20:63244..62948788 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 copy number gain not provided [RCV000741059] Chr20:63244..62961294 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_181659.3(NCOA3):c.3792A>G (p.Gln1264=) single nucleotide variant not provided [RCV000949853] Chr20:47651122 [GRCh38]
Chr20:46279866 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.3132G>A (p.Leu1044=) single nucleotide variant not provided [RCV000915991] Chr20:47642264 [GRCh38]
Chr20:46271008 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.836A>G (p.Asn279Ser) single nucleotide variant not specified [RCV004284344] Chr20:47633508 [GRCh38]
Chr20:46262252 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1675C>T (p.Pro559Ser) single nucleotide variant not provided [RCV000955584] Chr20:47636061 [GRCh38]
Chr20:46264805 [GRCh37]
Chr20:20q13.12		 benign
Single allele deletion Focal-onset seizure [RCV001004039] Chr20:34980430..46806549 [GRCh37]
Chr20:20q11.23-13.13		 likely pathogenic
GRCh37/hg19 20q13.12-13.13(chr20:46147529-46438075)x3 copy number gain not provided [RCV001834398] Chr20:46147529..46438075 [GRCh37]
Chr20:20q13.12-13.13		 uncertain significance
NM_181659.3(NCOA3):c.2810C>G (p.Ser937Cys) single nucleotide variant Bilateral sensorineural hearing impairment [RCV001730852] Chr20:47639679 [GRCh38]
Chr20:46268423 [GRCh37]
Chr20:20q13.12		 pathogenic
GRCh37/hg19 20q13.12-13.13(chr20:42985044-48599046)x1 copy number loss Developmental and epileptic encephalopathy, 26 [RCV001801198] Chr20:42985044..48599046 [GRCh37]
Chr20:20q13.12-13.13		 pathogenic
GRCh37/hg19 20q13.12(chr20:45626379-46257019)x3 copy number gain not provided [RCV001833045] Chr20:45626379..46257019 [GRCh37]
Chr20:20q13.12		 uncertain significance
GRCh37/hg19 20q13.12-13.13(chr20:46203730-46521403)x3 copy number gain not provided [RCV002474997] Chr20:46203730..46521403 [GRCh37]
Chr20:20q13.12-13.13		 uncertain significance
NM_181659.3(NCOA3):c.4028C>T (p.Ser1343Phe) single nucleotide variant not specified [RCV004192120] Chr20:47652487 [GRCh38]
Chr20:46281231 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3359C>T (p.Pro1120Leu) single nucleotide variant not specified [RCV004113593] Chr20:47647179 [GRCh38]
Chr20:46275923 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3487C>T (p.Arg1163Trp) single nucleotide variant not specified [RCV004226521] Chr20:47647307 [GRCh38]
Chr20:46276051 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.476A>G (p.Asn159Ser) single nucleotide variant not specified [RCV004136961] Chr20:47627120 [GRCh38]
Chr20:46255864 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.106C>T (p.Arg36Trp) single nucleotide variant not specified [RCV004224384] Chr20:47623933 [GRCh38]
Chr20:46252677 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.1424C>G (p.Pro475Arg) single nucleotide variant not specified [RCV004240405] Chr20:47635633 [GRCh38]
Chr20:46264377 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1670C>T (p.Thr557Ile) single nucleotide variant not specified [RCV004100827] Chr20:47636056 [GRCh38]
Chr20:46264800 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1166C>T (p.Pro389Leu) single nucleotide variant not specified [RCV004170057] Chr20:47635375 [GRCh38]
Chr20:46264119 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1344G>A (p.Met448Ile) single nucleotide variant not specified [RCV004086107] Chr20:47635553 [GRCh38]
Chr20:46264297 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.457G>C (p.Val153Leu) single nucleotide variant not specified [RCV004142828] Chr20:47627101 [GRCh38]
Chr20:46255845 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2324C>G (p.Pro775Arg) single nucleotide variant not specified [RCV004226925] Chr20:47636710 [GRCh38]
Chr20:46265454 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1390A>G (p.Ser464Gly) single nucleotide variant not specified [RCV004242340] Chr20:47635599 [GRCh38]
Chr20:46264343 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2255C>T (p.Ser752Phe) single nucleotide variant not specified [RCV004161499] Chr20:47636641 [GRCh38]
Chr20:46265385 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2926C>G (p.Gln976Glu) single nucleotide variant not specified [RCV004175893] Chr20:47639795 [GRCh38]
Chr20:46268539 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1417C>T (p.Leu473Phe) single nucleotide variant not specified [RCV004150150] Chr20:47635626 [GRCh38]
Chr20:46264370 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.32T>C (p.Leu11Pro) single nucleotide variant not specified [RCV004246578] Chr20:47622279 [GRCh38]
Chr20:46251023 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.973A>G (p.Asn325Asp) single nucleotide variant not specified [RCV004215766] Chr20:47634056 [GRCh38]
Chr20:46262800 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3607G>A (p.Ala1203Thr) single nucleotide variant not specified [RCV004130234] Chr20:47649065 [GRCh38]
Chr20:46277809 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3000A>T (p.Gln1000His) single nucleotide variant not specified [RCV004207870] Chr20:47639971 [GRCh38]
Chr20:46268715 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3144T>G (p.Ser1048Arg) single nucleotide variant not specified [RCV004174870] Chr20:47642276 [GRCh38]
Chr20:46271020 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2590G>A (p.Val864Ile) single nucleotide variant not specified [RCV004237150] Chr20:47639085 [GRCh38]
Chr20:46267829 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3500C>G (p.Pro1167Arg) single nucleotide variant not specified [RCV004120555] Chr20:47647320 [GRCh38]
Chr20:46276064 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3374G>A (p.Gly1125Asp) single nucleotide variant not specified [RCV004189053] Chr20:47647194 [GRCh38]
Chr20:46275938 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1403A>G (p.His468Arg) single nucleotide variant not specified [RCV004075045] Chr20:47635612 [GRCh38]
Chr20:46264356 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1654C>T (p.Pro552Ser) single nucleotide variant not specified [RCV004089284] Chr20:47636040 [GRCh38]
Chr20:46264784 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3248A>G (p.Asn1083Ser) single nucleotide variant not specified [RCV004296733] Chr20:47642380 [GRCh38]
Chr20:46271124 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.560C>A (p.Thr187Asn) single nucleotide variant not specified [RCV004259319] Chr20:47627588 [GRCh38]
Chr20:46256332 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3592C>G (p.Pro1198Ala) single nucleotide variant not specified [RCV004253407] Chr20:47649050 [GRCh38]
Chr20:46277794 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.419A>G (p.Asn140Ser) single nucleotide variant not specified [RCV004308686] Chr20:47627063 [GRCh38]
Chr20:46255807 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2533G>C (p.Val845Leu) single nucleotide variant not specified [RCV004270464] Chr20:47639028 [GRCh38]
Chr20:46267772 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3892G>A (p.Gly1298Arg) single nucleotide variant not specified [RCV004249828] Chr20:47651222 [GRCh38]
Chr20:46279966 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2875C>G (p.Pro959Ala) single nucleotide variant not specified [RCV004268474] Chr20:47639744 [GRCh38]
Chr20:46268488 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3425T>G (p.Met1142Arg) single nucleotide variant not specified [RCV004361561] Chr20:47647245 [GRCh38]
Chr20:46275989 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3341C>G (p.Thr1114Arg) single nucleotide variant not specified [RCV004349023] Chr20:47647161 [GRCh38]
Chr20:46275905 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3385C>G (p.Gln1129Glu) single nucleotide variant not specified [RCV004348954] Chr20:47647205 [GRCh38]
Chr20:46275949 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3759G>A (p.Gln1253=) single nucleotide variant not provided [RCV003440429] Chr20:47651089 [GRCh38]
Chr20:46279833 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.3786G>A (p.Gln1262=) single nucleotide variant not provided [RCV003431346] Chr20:47651116 [GRCh38]
Chr20:46279860 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.3016C>T (p.Gln1006Ter) single nucleotide variant not provided [RCV003431345] Chr20:47639987 [GRCh38]
Chr20:46268731 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3741GCA[4] (p.Gln1274_Gln1276del) microsatellite not provided [RCV003668634] Chr20:47651071..47651079 [GRCh38]
Chr20:46279815..46279823 [GRCh37]
Chr20:20q13.12		 benign
NM_181659.3(NCOA3):c.1001G>A (p.Arg334Gln) single nucleotide variant not specified [RCV004476527] Chr20:47634084 [GRCh38]
Chr20:46262828 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1055T>G (p.Phe352Cys) single nucleotide variant not specified [RCV004476529] Chr20:47634138 [GRCh38]
Chr20:46262882 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1685T>C (p.Val562Ala) single nucleotide variant not specified [RCV004476564] Chr20:47636071 [GRCh38]
Chr20:46264815 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2588C>G (p.Ser863Cys) single nucleotide variant not specified [RCV004476588] Chr20:47639083 [GRCh38]
Chr20:46267827 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2594G>A (p.Gly865Asp) single nucleotide variant not specified [RCV004476592] Chr20:47639089 [GRCh38]
Chr20:46267833 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1895G>A (p.Arg632Gln) single nucleotide variant not specified [RCV004476566] Chr20:47636281 [GRCh38]
Chr20:46265025 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.328A>G (p.Lys110Glu) single nucleotide variant not specified [RCV004476615] Chr20:47625452 [GRCh38]
Chr20:46254196 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1588A>C (p.Ser530Arg) single nucleotide variant not specified [RCV004476554] Chr20:47635974 [GRCh38]
Chr20:46264718 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.272A>T (p.Asn91Ile) single nucleotide variant not specified [RCV004476600] Chr20:47625396 [GRCh38]
Chr20:46254140 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2621G>A (p.Ser874Asn) single nucleotide variant not specified [RCV004476597] Chr20:47639116 [GRCh38]
Chr20:46267860 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3412A>G (p.Met1138Val) single nucleotide variant not specified [RCV004476626] Chr20:47647232 [GRCh38]
Chr20:46275976 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3998A>T (p.Asn1333Ile) single nucleotide variant not specified [RCV004476659] Chr20:47652457 [GRCh38]
Chr20:46281201 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.659G>T (p.Arg220Ile) single nucleotide variant not specified [RCV004476679] Chr20:47627687 [GRCh38]
Chr20:46256431 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.789C>A (p.Asn263Lys) single nucleotide variant not specified [RCV004476681] Chr20:47627989 [GRCh38]
Chr20:46256733 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1246G>A (p.Ala416Thr) single nucleotide variant not specified [RCV004641330] Chr20:47635455 [GRCh38]
Chr20:46264199 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.3543G>C (p.Gln1181His) single nucleotide variant not specified [RCV004654523] Chr20:47647363 [GRCh38]
Chr20:46276107 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.961G>C (p.Glu321Gln) single nucleotide variant not specified [RCV004654524] Chr20:47633633 [GRCh38]
Chr20:46262377 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3869C>T (p.Pro1290Leu) single nucleotide variant not specified [RCV004654525] Chr20:47651199 [GRCh38]
Chr20:46279943 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3959A>C (p.Gln1320Pro) single nucleotide variant not specified [RCV004641331] Chr20:47652418 [GRCh38]
Chr20:46281162 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1852C>T (p.His618Tyr) single nucleotide variant not specified [RCV004641332] Chr20:47636238 [GRCh38]
Chr20:46264982 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.52C>T (p.Arg18Cys) single nucleotide variant not specified [RCV004654517] Chr20:47622299 [GRCh38]
Chr20:46251043 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1056C>G (p.Phe352Leu) single nucleotide variant not specified [RCV004654518] Chr20:47634139 [GRCh38]
Chr20:46262883 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3364A>G (p.Met1122Val) single nucleotide variant not specified [RCV004654519] Chr20:47647184 [GRCh38]
Chr20:46275928 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.2239C>A (p.Pro747Thr) single nucleotide variant not specified [RCV004654520] Chr20:47636625 [GRCh38]
Chr20:46265369 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3935A>C (p.Gln1312Pro) single nucleotide variant not specified [RCV004654521] Chr20:47651265 [GRCh38]
Chr20:46280009 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.1205G>C (p.Ser402Thr) single nucleotide variant not specified [RCV004654526] Chr20:47635414 [GRCh38]
Chr20:46264158 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3653A>G (p.Gln1218Arg) single nucleotide variant not specified [RCV004654527] Chr20:47650983 [GRCh38]
Chr20:46279727 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.1942G>C (p.Glu648Gln) single nucleotide variant not specified [RCV004476572] Chr20:47636328 [GRCh38]
Chr20:46265072 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.4053G>A (p.Pro1351=) single nucleotide variant not specified [RCV004476664] Chr20:47652512 [GRCh38]
Chr20:46281256 [GRCh37]
Chr20:20q13.12		 likely benign
NM_181659.3(NCOA3):c.949C>T (p.Arg317Cys) single nucleotide variant not specified [RCV004476683] Chr20:47633621 [GRCh38]
Chr20:46262365 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3467G>A (p.Arg1156Gln) single nucleotide variant not specified [RCV004476633] Chr20:47647287 [GRCh38]
Chr20:46276031 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3716G>A (p.Arg1239Gln) single nucleotide variant not specified [RCV004476644] Chr20:47651046 [GRCh38]
Chr20:46279790 [GRCh37]
Chr20:20q13.12		 uncertain significance
NM_181659.3(NCOA3):c.3830C>G (p.Thr1277Ser) single nucleotide variant not specified [RCV004476647] Chr20:47651160 [GRCh38]
Chr20:46279904 [GRCh37]
Chr20:20q13.12		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR18Ahsa-miR-18a-5pMirtarbaseexternal_infoWestern blotNon-Functional MTI19706389
MIR19B2hsa-miR-19b-3pMirtarbaseexternal_infoWestern blotNon-Functional MTI19706389
MIR19B1hsa-miR-19b-3pMirtarbaseexternal_infoWestern blotNon-Functional MTI19706389
MIR17hsa-miR-17-5pMirtarbaseexternal_infoLuciferase reporter assay//Northern blot//qRT-PCR/Functional MTI16940181
MIR17hsa-miR-17-5pTarbaseexternal_infoWesternblitPOSITIVE
MIR17hsa-miR-17-5pTarbaseexternal_infoqPCRNEGATIVE
MIR17hsa-miR-17-5pTarbaseexternal_infoNothernblot NEGATIVE
MIR17hsa-miR-17-5pMirecordsexternal_info{unchanged}NA16940181
MIR17hsa-miR-17-5pOncomiRDBexternal_infoNANA23436804
MIR17hsa-miR-17-5pOncomiRDBexternal_infoNANA16940181

Predicted Target Of
Summary Value
Count of predictions:3664
Count of miRNA genes:923
Interacting mature miRNAs:1072
Transcripts:ENST00000341724, ENST00000371997, ENST00000371998, ENST00000372004, ENST00000490248, ENST00000497292
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
2292864PRSTS43_HProstate tumor susceptibility QTL 43 (human)0.620.05Prostate tumor susceptibility204730303964444167Human
1300007BP29_HBlood pressure QTL 29 (human)Blood pressurehypertension susceptibility203653600562536005Human
407182851GWAS831827_Hlanguage measurement QTL GWAS831827 (human)0.000002language measurement204764582947645830Human
407020872GWAS669848_Hacute lymphoblastic leukemia, response to antineoplastic agent QTL GWAS669848 (human)0.000002acute lymphoblastic leukemia, response to antineoplastic agent204757986147579862Human
407045689GWAS694665_Hplatelet count QTL GWAS694665 (human)9e-14platelet quantity (VT:0003179)platelet count (CMO:0000029)204759992347599924Human
407272940GWAS921916_Hbody height QTL GWAS921916 (human)1e-46body height (VT:0001253)body height (CMO:0000106)204759992347599924Human
407044990GWAS693966_Hplatelet count QTL GWAS693966 (human)1e-14platelet quantity (VT:0003179)platelet count (CMO:0000029)204759992347599924Human
407081150GWAS730126_Htotal blood protein measurement QTL GWAS730126 (human)1e-08total blood protein measurementblood protein measurement (CMO:0000028)204765108347651084Human
406925022GWAS573998_Hhigh density lipoprotein cholesterol measurement QTL GWAS573998 (human)7e-11high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)204759031447590315Human

Markers in Region
D20S197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,160,768 - 46,160,954UniSTSGRCh37
GRCh372046,160,764 - 46,160,903UniSTSGRCh37
Build 362045,594,175 - 45,594,361RGDNCBI36
Celera2042,874,406 - 42,874,592RGD
Celera2042,874,402 - 42,874,541UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map20q12-q13.1UniSTS
HuRef2042,902,312 - 42,902,506UniSTS
HuRef2042,902,308 - 42,902,455UniSTS
Marshfield Genetic Map2066.16UniSTS
Marshfield Genetic Map2066.16RGD
Genethon Genetic Map2066.0UniSTS
TNG Radiation Hybrid Map2021634.0UniSTS
deCODE Assembly Map2073.4UniSTS
Stanford-G3 RH Map202378.0UniSTS
GeneMap99-GB4 RH Map20265.9UniSTS
Whitehead-YAC Contig Map20 UniSTS
NCBI RH Map20492.2UniSTS
GeneMap99-G3 RH Map202411.0UniSTS
WI-21757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,285,506 - 46,285,606UniSTSGRCh37
Build 362045,718,913 - 45,719,013RGDNCBI36
Celera2042,999,159 - 42,999,259RGD
Cytogenetic Map20q12UniSTS
HuRef2043,026,834 - 43,026,934UniSTS
GeneMap99-GB4 RH Map20267.81UniSTS
Whitehead-RH Map20298.9UniSTS
RH12403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,282,284 - 46,282,466UniSTSGRCh37
Build 362045,715,691 - 45,715,873RGDNCBI36
Celera2042,995,937 - 42,996,119RGD
Cytogenetic Map20q12UniSTS
HuRef2043,023,612 - 43,023,794UniSTS
GeneMap99-GB4 RH Map20267.81UniSTS
Z94499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,278,907 - 46,278,997UniSTSGRCh37
Build 362045,712,314 - 45,712,404RGDNCBI36
Celera2042,992,560 - 42,992,650RGD
Cytogenetic Map20q12UniSTS
HuRef2043,020,144 - 43,020,234UniSTS
Z94341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,203,947 - 46,204,027UniSTSGRCh37
Build 362045,637,354 - 45,637,434RGDNCBI36
Celera2042,917,601 - 42,917,681RGD
Cytogenetic Map20q12UniSTS
HuRef2042,945,201 - 42,945,281UniSTS
D20S1123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,282,258 - 46,282,391UniSTSGRCh37
Build 362045,715,665 - 45,715,798RGDNCBI36
Celera2042,995,911 - 42,996,044RGD
Cytogenetic Map20q12UniSTS
HuRef2043,023,586 - 43,023,719UniSTS
SHGC-58803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,283,345 - 46,283,494UniSTSGRCh37
Build 362045,716,752 - 45,716,901RGDNCBI36
Celera2042,996,998 - 42,997,147RGD
Cytogenetic Map20q12UniSTS
HuRef2043,024,673 - 43,024,822UniSTS
TNG Radiation Hybrid Map2021657.0UniSTS
RH48397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,283,093 - 46,283,277UniSTSGRCh37
Build 362045,716,500 - 45,716,684RGDNCBI36
Celera2042,996,746 - 42,996,930RGD
Cytogenetic Map20q12UniSTS
HuRef2043,024,421 - 43,024,605UniSTS
GeneMap99-GB4 RH Map20267.81UniSTS
RH18152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,282,161 - 46,282,348UniSTSGRCh37
Build 362045,715,568 - 45,715,755RGDNCBI36
Celera2042,995,814 - 42,996,001RGD
Cytogenetic Map20q12UniSTS
HuRef2043,023,489 - 43,023,676UniSTS
PMC113761P3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,281,164 - 46,281,797UniSTSGRCh37
Build 362045,714,571 - 45,715,204RGDNCBI36
Celera2042,994,817 - 42,995,450RGD
Cytogenetic Map20q12UniSTS
HuRef2043,022,492 - 43,023,125UniSTS
NCOA3_1532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,283,823 - 46,284,486UniSTSGRCh37
Build 362045,717,230 - 45,717,893RGDNCBI36
Celera2042,997,476 - 42,998,139RGD
HuRef2043,025,151 - 43,025,814UniSTS
G01531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,131,889 - 46,132,039UniSTSGRCh37
Build 362045,565,296 - 45,565,446RGDNCBI36
Celera2042,845,517 - 42,845,667RGD
Cytogenetic Map20q12UniSTS
HuRef2042,873,621 - 42,873,771UniSTS
Z94538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,251,925 - 46,252,114UniSTSGRCh37
Build 362045,685,332 - 45,685,521RGDNCBI36
Celera2042,965,581 - 42,965,770RGD
Cytogenetic Map20q12UniSTS
HuRef2042,993,163 - 42,993,352UniSTS
D20S542E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,285,193 - 46,285,302UniSTSGRCh37
Build 362045,718,600 - 45,718,709RGDNCBI36
Celera2042,998,846 - 42,998,955RGD
Cytogenetic Map20q12UniSTS
HuRef2043,026,521 - 43,026,630UniSTS
GeneMap99-GB4 RH Map20267.81UniSTS
STS-H52110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,284,262 - 46,284,410UniSTSGRCh37
Build 362045,717,669 - 45,717,817RGDNCBI36
Celera2042,997,915 - 42,998,063RGD
Cytogenetic Map20q12UniSTS
HuRef2043,025,590 - 43,025,738UniSTS
GeneMap99-GB4 RH Map20267.81UniSTS
NCBI RH Map20492.2UniSTS
D20S951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,279,733 - 46,279,882UniSTSGRCh37
Build 362045,713,140 - 45,713,289RGDNCBI36
Celera2042,993,386 - 42,993,535RGD
Cytogenetic Map20q12UniSTS
HuRef2043,021,064 - 43,021,210UniSTS
Whitehead-RH Map20305.7UniSTS
AL031468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372046,145,157 - 46,145,289UniSTSGRCh37
Build 362045,578,564 - 45,578,696RGDNCBI36
Celera2042,858,793 - 42,858,925RGD
Cytogenetic Map20q12UniSTS
HuRef2042,886,870 - 42,887,002UniSTS
G64267  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map20q12UniSTS
D20S197  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map20q12UniSTS
TNG Radiation Hybrid Map2021634.0UniSTS
Stanford-G3 RH Map202378.0UniSTS
NCBI RH Map20492.2UniSTS
GeneMap99-G3 RH Map202411.0UniSTS


Sequence

Nucleotide Sequences
RefSeq Transcripts NG_016810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001174087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001174088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_181659 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF010227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF012108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF016031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF036892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL021394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL034418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC092516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC119001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC122547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM692321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU588121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA450268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB091786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF488684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000371997   ⟹   ENSP00000361065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2047,501,941 - 47,655,742 (+)Ensembl
Ensembl Acc Id: ENST00000371998   ⟹   ENSP00000361066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2047,501,887 - 47,656,872 (+)Ensembl
Ensembl Acc Id: ENST00000372004   ⟹   ENSP00000361073
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2047,501,902 - 47,656,877 (+)Ensembl
Ensembl Acc Id: ENST00000490248
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2047,622,958 - 47,624,073 (+)Ensembl
Ensembl Acc Id: ENST00000497292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2047,627,002 - 47,628,790 (+)Ensembl
RefSeq Acc Id: NM_001174087   ⟹   NP_001167558
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382047,501,887 - 47,656,872 (+)NCBI
GRCh372046,130,601 - 46,285,621 (+)ENTREZGENE
HuRef2042,872,332 - 43,026,949 (+)ENTREZGENE
CHM1_12046,033,477 - 46,188,916 (+)NCBI
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001174088   ⟹   NP_001167559
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382047,501,887 - 47,656,872 (+)NCBI
GRCh372046,130,601 - 46,285,621 (+)ENTREZGENE
HuRef2042,872,332 - 43,026,949 (+)ENTREZGENE
CHM1_12046,033,477 - 46,188,916 (+)NCBI
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBI
Sequence:
RefSeq Acc Id: NM_006534   ⟹   NP_006525
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382047,501,887 - 47,656,872 (+)NCBI
GRCh372046,130,601 - 46,285,621 (+)ENTREZGENE
Build 362045,564,064 - 45,719,023 (+)NCBI Archive
HuRef2042,872,332 - 43,026,949 (+)ENTREZGENE
CHM1_12046,033,477 - 46,188,916 (+)NCBI
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBI
Sequence:
RefSeq Acc Id: NM_181659   ⟹   NP_858045
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382047,501,887 - 47,656,872 (+)NCBI
GRCh372046,130,601 - 46,285,621 (+)ENTREZGENE
Build 362045,564,064 - 45,719,023 (+)NCBI Archive
HuRef2042,872,332 - 43,026,949 (+)ENTREZGENE
CHM1_12046,033,477 - 46,188,916 (+)NCBI
T2T-CHM13v2.02049,240,095 - 49,395,274 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001167558 (Get FASTA)   NCBI Sequence Viewer  
  NP_001167559 (Get FASTA)   NCBI Sequence Viewer  
  NP_006525 (Get FASTA)   NCBI Sequence Viewer  
  NP_858045 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB92368 (Get FASTA)   NCBI Sequence Viewer  
  AAC51663 (Get FASTA)   NCBI Sequence Viewer  
  AAC51677 (Get FASTA)   NCBI Sequence Viewer  
  AAC51849 (Get FASTA)   NCBI Sequence Viewer  
  AAH92516 (Get FASTA)   NCBI Sequence Viewer  
  AAI19002 (Get FASTA)   NCBI Sequence Viewer  
  AAI22548 (Get FASTA)   NCBI Sequence Viewer  
  ABO43042 (Get FASTA)   NCBI Sequence Viewer  
  BAD93100 (Get FASTA)   NCBI Sequence Viewer  
  BAF82372 (Get FASTA)   NCBI Sequence Viewer  
  BAG59383 (Get FASTA)   NCBI Sequence Viewer  
  BAG63841 (Get FASTA)   NCBI Sequence Viewer  
  BAG63847 (Get FASTA)   NCBI Sequence Viewer  
  EAW75696 (Get FASTA)   NCBI Sequence Viewer  
  EAW75697 (Get FASTA)   NCBI Sequence Viewer  
  EAW75698 (Get FASTA)   NCBI Sequence Viewer  
  EAW75699 (Get FASTA)   NCBI Sequence Viewer  
  EAW75700 (Get FASTA)   NCBI Sequence Viewer  
  EAW75701 (Get FASTA)   NCBI Sequence Viewer  
  EAW75702 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000361065
  ENSP00000361065.3
  ENSP00000361066
  ENSP00000361066.3
  ENSP00000361073
  ENSP00000361073.1
GenBank Protein Q9Y6Q9 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001167559   ⟸   NM_001174088
- Peptide Label: isoform d
- UniProtKB: Q0IIN7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_858045   ⟸   NM_181659
- Peptide Label: isoform a
- UniProtKB: Q9UPG4 (UniProtKB/Swiss-Prot),   Q9UPC9 (UniProtKB/Swiss-Prot),   Q9BR49 (UniProtKB/Swiss-Prot),   Q5JYE0 (UniProtKB/Swiss-Prot),   Q5JYD9 (UniProtKB/Swiss-Prot),   Q0VF45 (UniProtKB/Swiss-Prot),   A4LAZ5 (UniProtKB/Swiss-Prot),   Q9UPG7 (UniProtKB/Swiss-Prot),   Q9Y6Q9 (UniProtKB/Swiss-Prot),   A8K0W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001167558   ⟸   NM_001174087
- Peptide Label: isoform c
- UniProtKB: Q569F6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_006525   ⟸   NM_006534
- Peptide Label: isoform b
- UniProtKB: Q0IIN7 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000361065   ⟸   ENST00000371997
Ensembl Acc Id: ENSP00000361066   ⟸   ENST00000371998
Ensembl Acc Id: ENSP00000361073   ⟸   ENST00000372004
Protein Domains
bHLH   PAS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y6Q9-F1-model_v2 AlphaFold Q9Y6Q9 1-1424 view protein structure

Promoters
RGD ID:6798873
Promoter ID:HG_KWN:39725
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000341724,   ENST00000372004,   NM_001174087,   NM_001174088,   NM_006534,   NM_181659,   UC002XTM.1,   UC010GHT.1,   UC010GHU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362045,563,806 - 45,566,017 (+)MPROMDB
RGD ID:6798859
Promoter ID:HG_KWN:39728
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000080407
Position:
Human AssemblyChrPosition (strand)Source
Build 362045,688,666 - 45,689,166 (+)MPROMDB
RGD ID:13207197
Promoter ID:EPDNEW_H27179
Type:initiation region
Name:NCOA3_1
Description:nuclear receptor coactivator 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382047,501,887 - 47,501,947EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7670 AgrOrtholog
COSMIC NCOA3 COSMIC
Ensembl Genes ENSG00000124151 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000371997 ENTREZGENE
  ENST00000371997.3 UniProtKB/Swiss-Prot
  ENST00000371998 ENTREZGENE
  ENST00000371998.8 UniProtKB/Swiss-Prot
  ENST00000372004 ENTREZGENE
  ENST00000372004.7 UniProtKB/Swiss-Prot
Gene3D-CATH 4.10.280.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  6.10.140.410 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000124151 GTEx
HGNC ID HGNC:7670 ENTREZGENE
Human Proteome Map NCOA3 Human Proteome Map
InterPro bHLH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DUF1518 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DUF4927 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HLH_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuc_rcpt_coact UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuc_rcpt_coact_Ncoa-typ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuc_rcpt_coact_Ncoa_int_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuclear_rcpt_coactivator UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SRC/p160_LXXLL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8202 UniProtKB/Swiss-Prot
NCBI Gene 8202 ENTREZGENE
OMIM 601937 OMIM
PANTHER PTHR10684 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10684:SF3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUF1518 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DUF4927 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NCOA_u2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nuc_rec_co-act UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS_11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SRC-1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB NCOA3 RGD, PharmGKB
PIRSF Nuclear_receptor_coactivator UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE BHLH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DUF1518 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HLH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47459 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF55785 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF69125 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A4LAZ5 ENTREZGENE
  A8K0W8 ENTREZGENE, UniProtKB/TrEMBL
  NCOA3_HUMAN UniProtKB/Swiss-Prot
  Q0IIN7 ENTREZGENE, UniProtKB/TrEMBL
  Q0VF45 ENTREZGENE
  Q569F6 ENTREZGENE, UniProtKB/TrEMBL
  Q59EE8_HUMAN UniProtKB/TrEMBL
  Q5JYD9 ENTREZGENE
  Q5JYE0 ENTREZGENE
  Q9BR49 ENTREZGENE
  Q9UPC9 ENTREZGENE
  Q9UPG4 ENTREZGENE
  Q9UPG7 ENTREZGENE
  Q9Y6Q9 ENTREZGENE
UniProt Secondary A4LAZ5 UniProtKB/Swiss-Prot
  Q0VF45 UniProtKB/Swiss-Prot
  Q5JYD9 UniProtKB/Swiss-Prot
  Q5JYE0 UniProtKB/Swiss-Prot
  Q9BR49 UniProtKB/Swiss-Prot
  Q9UPC9 UniProtKB/Swiss-Prot
  Q9UPG4 UniProtKB/Swiss-Prot
  Q9UPG7 UniProtKB/Swiss-Prot