SRA1 (steroid receptor RNA activator 1) - Rat Genome Database

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Gene: SRA1 (steroid receptor RNA activator 1) Homo sapiens
Analyze
Symbol: SRA1
Name: steroid receptor RNA activator 1
RGD ID: 1353576
HGNC Page HGNC:11281
Description: Enables steroid receptor RNA activator RNA binding activity and transcription coactivator activity. Involved in several processes, including cellular response to estrogen stimulus; negative regulation of myoblast differentiation; and regulation of mitotic cell cycle. Located in several cellular components, including intercellular bridge; microtubule cytoskeleton; and nucleoplasm. Part of SCAR complex and ribonucleoprotein complex. Biomarker of congestive heart failure.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MGC87674; pp7684; SRA; SRAP; steriod receptor RNA activator 1; steriod receptor RNA activator protein; steroid receptor coactivator; steroid receptor RNA activator 1 (complexes with NCOA1); steroid receptor RNA activator protein; STRAA1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,550,067 - 140,558,093 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,537,340 - 140,557,677 (-)EnsemblGRCh38hg38GRCh38
GRCh375139,929,652 - 139,937,678 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365139,909,837 - 139,917,862 (-)NCBINCBI36Build 36hg18NCBI36
Build 345139,910,273 - 139,917,220NCBI
Celera5136,006,404 - 136,014,428 (-)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,074,991 - 135,083,015 (-)NCBIHuRef
CHM1_15139,362,900 - 139,370,926 (-)NCBICHM1_1
T2T-CHM13v2.05141,075,497 - 141,083,524 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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. Long noncoding RNA dysregulation in ischemic heart failure. Greco S, etal., J Transl Med. 2016 Jun 18;14(1):183. doi: 10.1186/s12967-016-0926-5.
2. Coregulators in nuclear estrogen receptor action: from concept to therapeutic targeting. Hall JM and McDonnell DP, Mol Interv. 2005 Dec;5(6):343-57.
3. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10199399   PMID:10485452   PMID:11103781   PMID:11331609   PMID:11818499   PMID:12118039   PMID:12163482   PMID:12444263   PMID:12477932   PMID:12565891   PMID:12909012   PMID:12943696  
PMID:14517287   PMID:14702039   PMID:14715875   PMID:15147866   PMID:15180993   PMID:15327771   PMID:15351741   PMID:15489334   PMID:15498874   PMID:15607539   PMID:16152589   PMID:16169070  
PMID:16344560   PMID:16540468   PMID:16607388   PMID:16773180   PMID:16848684   PMID:17702747   PMID:18560548   PMID:18676680   PMID:18950845   PMID:19064572   PMID:19064678   PMID:19188450  
PMID:19483093   PMID:19625176   PMID:19692168   PMID:19740422   PMID:20079837   PMID:20153324   PMID:20219889   PMID:20301509   PMID:20398657   PMID:20677014   PMID:20855289   PMID:20966046  
PMID:21771633   PMID:21807064   PMID:21873635   PMID:22362738   PMID:22939629   PMID:22998747   PMID:23579816   PMID:23749764   PMID:23907597   PMID:24486609   PMID:24486611   PMID:25609053  
PMID:26344197   PMID:26496121   PMID:26496610   PMID:26581859   PMID:26638075   PMID:26967566   PMID:27086651   PMID:27282881   PMID:27406387   PMID:27694140   PMID:28085012   PMID:29039612  
PMID:30272285   PMID:31106680   PMID:31540324   PMID:31714481   PMID:32783135   PMID:33000206   PMID:33277362   PMID:33572095   PMID:33961781   PMID:34402503   PMID:34520769   PMID:34597346  
PMID:34685582   PMID:34967547   PMID:35119092   PMID:35695662   PMID:35831314   PMID:35944360   PMID:36552771   PMID:37143083  


Genomics

Comparative Map Data
SRA1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,550,067 - 140,558,093 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,537,340 - 140,557,677 (-)EnsemblGRCh38hg38GRCh38
GRCh375139,929,652 - 139,937,678 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365139,909,837 - 139,917,862 (-)NCBINCBI36Build 36hg18NCBI36
Build 345139,910,273 - 139,917,220NCBI
Celera5136,006,404 - 136,014,428 (-)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,074,991 - 135,083,015 (-)NCBIHuRef
CHM1_15139,362,900 - 139,370,926 (-)NCBICHM1_1
T2T-CHM13v2.05141,075,497 - 141,083,524 (-)NCBIT2T-CHM13v2.0
Sra1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391836,800,240 - 36,803,364 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1836,799,734 - 36,803,868 (-)EnsemblGRCm39 Ensembl
GRCm381836,667,187 - 36,670,311 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1836,666,681 - 36,670,815 (-)EnsemblGRCm38mm10GRCm38
MGSCv371836,826,841 - 36,829,965 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361836,793,221 - 36,796,269 (-)NCBIMGSCv36mm8
Celera1837,116,277 - 37,119,407 (-)NCBICelera
Cytogenetic Map18B2NCBI
cM Map1819.46NCBI
Sra1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81828,543,347 - 28,547,474 (-)NCBIGRCr8
mRatBN7.21828,269,192 - 28,273,023 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1828,269,311 - 28,272,538 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1828,396,455 - 28,399,683 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01829,158,546 - 29,161,774 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01828,493,784 - 28,497,012 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01829,494,004 - 29,497,232 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1829,494,014 - 29,497,410 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01829,199,078 - 29,202,306 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41829,306,555 - 29,309,783 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11829,333,370 - 29,336,429 (-)NCBI
Celera1827,996,484 - 27,999,712 (-)NCBICelera
Cytogenetic Map18p11NCBI
Sra1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955418126,726 - 133,316 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955418126,111 - 133,498 (+)NCBIChiLan1.0ChiLan1.0
SRA1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24135,808,039 - 135,815,645 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15133,947,590 - 133,955,302 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05135,914,506 - 135,922,704 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15142,032,113 - 142,040,137 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5142,032,119 - 142,039,188 (-)Ensemblpanpan1.1panPan2
SRA1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1235,745,518 - 35,752,497 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl235,745,877 - 35,752,502 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha232,783,751 - 32,790,730 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,200,151 - 36,207,129 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,200,510 - 36,207,134 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1233,253,022 - 33,260,000 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0234,120,557 - 34,127,539 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0234,873,253 - 34,880,232 (-)NCBIUU_Cfam_GSD_1.0
Sra1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213152,086,253 - 152,092,622 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365319,519,087 - 9,525,123 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365319,518,719 - 9,525,195 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SRA1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl2142,307,012 - 142,313,738 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.12142,307,009 - 142,314,613 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22148,250,853 - 148,257,575 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SRA1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12343,194,462 - 43,203,134 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2343,194,693 - 43,202,057 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603434,681,266 - 34,689,988 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sra1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474333,315,236 - 33,321,795 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474333,314,878 - 33,322,297 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SRA1
47 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
NM_006051.3(APBB3):c.828C>T (p.Ile276=) single nucleotide variant Malignant melanoma [RCV000066666] Chr5:140561390 [GRCh38]
Chr5:139940975 [GRCh37]
Chr5:139921159 [NCBI36]
Chr5:5q31.3
not provided
GRCh38/hg38 5q31.2-31.3(chr5:137836682-140696361)x3 copy number gain See cases [RCV000134725] Chr5:137836682..140696361 [GRCh38]
Chr5:137172371..140075946 [GRCh37]
Chr5:137200270..140056130 [NCBI36]
Chr5:5q31.2-31.3
pathogenic
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q31.3(chr5:139931607-139936835)x1 copy number loss not provided [RCV000745193] Chr5:139931607..139936835 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931607-139937146)x1 copy number loss not provided [RCV000745194] Chr5:139931607..139937146 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931607-139938303)x1 copy number loss not provided [RCV000745195] Chr5:139931607..139938303 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931607-139938337)x1 copy number loss not provided [RCV000745196] Chr5:139931607..139938337 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931613-139931661)x1 copy number loss not provided [RCV000745197] Chr5:139931613..139931661 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931613-139931739)x1 copy number loss not provided [RCV000745198] Chr5:139931613..139931739 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:139931623-139931740)x3 copy number gain not provided [RCV000745199] Chr5:139931623..139931740 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.653C>T (p.Pro218Leu) single nucleotide variant not provided [RCV000966966] Chr5:140550722 [GRCh38]
Chr5:139930307 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.48C>T (p.Asn16=) single nucleotide variant not provided [RCV000966967] Chr5:140557250 [GRCh38]
Chr5:139936835 [GRCh37]
Chr5:5q31.3
benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NM_001035235.4(SRA1):c.291_292insC (p.Val98fs) insertion not provided [RCV000946877] Chr5:140552044..140552045 [GRCh38]
Chr5:139931629..139931630 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.2-31.3(chr5:139447779-140047037)x3 copy number gain not provided [RCV000846756] Chr5:139447779..140047037 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
NC_000005.9:g.(?_139930285)_(140078137_?)del deletion not provided [RCV003107704] Chr5:139930285..140078137 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.123C>A (p.Val41=) single nucleotide variant not provided [RCV001617254] Chr5:140557175 [GRCh38]
Chr5:139936760 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.152-9_152-8del deletion not provided [RCV001688812] Chr5:140552192..140552193 [GRCh38]
Chr5:139931777..139931778 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.151+49_151+51del deletion not provided [RCV001608697] Chr5:140557096..140557098 [GRCh38]
Chr5:139936681..139936683 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.292_293insAC (p.Val98fs) insertion not provided [RCV001676283] Chr5:140552043..140552044 [GRCh38]
Chr5:139931628..139931629 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.341G>A (p.Arg114His) single nucleotide variant Hypogonadism with anosmia [RCV000859989] Chr5:140551995 [GRCh38]
Chr5:139931580 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.152-161G>A single nucleotide variant not provided [RCV001686649] Chr5:140552345 [GRCh38]
Chr5:139931930 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.151+50_151+51del deletion not provided [RCV001713809] Chr5:140557096..140557097 [GRCh38]
Chr5:139936681..139936682 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.25+33T>C single nucleotide variant not provided [RCV001713547] Chr5:140557395 [GRCh38]
Chr5:139936980 [GRCh37]
Chr5:5q31.3
benign
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q31.2-31.3(chr5:139493717-140517454)x1 copy number loss PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001801202] Chr5:139493717..140517454 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
NM_001035235.4(SRA1):c.500T>C (p.Ile167Thr) single nucleotide variant not provided [RCV002264384]|not specified [RCV001733553] Chr5:140550875 [GRCh38]
Chr5:139930460 [GRCh37]
Chr5:5q31.3
benign|likely benign
NM_001035235.4(SRA1):c.58C>G (p.Gln20Glu) single nucleotide variant not provided [RCV001815945] Chr5:140557240 [GRCh38]
Chr5:139936825 [GRCh37]
Chr5:5q31.3
benign|conflicting interpretations of pathogenicity|uncertain significance
NR_045586.1(SRA1):n.617_624del deletion not provided [RCV001988522] Chr5:140557470..140557477 [GRCh38]
Chr5:139937055..139937062 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_001035235.4(SRA1):c.293_294del (p.Val98fs) microsatellite Amenorrhea [RCV001849747] Chr5:140552042..140552043 [GRCh38]
Chr5:139931627..139931628 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.405G>T (p.Gln135His) single nucleotide variant not provided [RCV001983115] Chr5:140551119 [GRCh38]
Chr5:139930704 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.373A>G (p.Ile125Val) single nucleotide variant not provided [RCV002035541] Chr5:140551151 [GRCh38]
Chr5:139930736 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.404A>C (p.Gln135Pro) single nucleotide variant not provided [RCV001972969] Chr5:140551120 [GRCh38]
Chr5:139930705 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.126C>G (p.Ala42=) single nucleotide variant not provided [RCV002128193] Chr5:140557172 [GRCh38]
Chr5:139936757 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.292_293insGAC (p.Val98delinsGlyLeu) insertion not provided [RCV002105377] Chr5:140552043..140552044 [GRCh38]
Chr5:139931628..139931629 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.182C>T (p.Pro61Leu) single nucleotide variant not provided [RCV002145083] Chr5:140552154 [GRCh38]
Chr5:139931739 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.383G>A (p.Arg128His) single nucleotide variant not provided [RCV002075470] Chr5:140551141 [GRCh38]
Chr5:139930726 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.152-10A>T single nucleotide variant not provided [RCV002088667] Chr5:140552194 [GRCh38]
Chr5:139931779 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.580A>G (p.Arg194Gly) single nucleotide variant not provided [RCV002167179] Chr5:140550795 [GRCh38]
Chr5:139930380 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.292G>C (p.Val98Leu) single nucleotide variant not provided [RCV002193754] Chr5:140552044 [GRCh38]
Chr5:139931629 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.413G>A (p.Gly138Glu) single nucleotide variant not provided [RCV002096385] Chr5:140551111 [GRCh38]
Chr5:139930696 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.486C>T (p.Asp162=) single nucleotide variant not provided [RCV002122793] Chr5:140550889 [GRCh38]
Chr5:139930474 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.230C>T (p.Pro77Leu) single nucleotide variant not provided [RCV002182702] Chr5:140552106 [GRCh38]
Chr5:139931691 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.151+7G>A single nucleotide variant not provided [RCV002180699] Chr5:140557140 [GRCh38]
Chr5:139936725 [GRCh37]
Chr5:5q31.3
likely benign
NC_000005.9:g.(?_136957787)_(140078137_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV003116437] Chr5:136957787..140078137 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
NM_001035235.4(SRA1):c.25+3G>C single nucleotide variant not provided [RCV003112035] Chr5:140557425 [GRCh38]
Chr5:139937010 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.128C>T (p.Ala43Val) single nucleotide variant Inborn genetic diseases [RCV003300937] Chr5:140557170 [GRCh38]
Chr5:139936755 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.196C>A (p.Pro66Thr) single nucleotide variant Inborn genetic diseases [RCV002772032] Chr5:140552140 [GRCh38]
Chr5:139931725 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.646A>G (p.Thr216Ala) single nucleotide variant Inborn genetic diseases [RCV002727913] Chr5:140550729 [GRCh38]
Chr5:139930314 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.157G>A (p.Ala53Thr) single nucleotide variant Inborn genetic diseases [RCV002865853] Chr5:140552179 [GRCh38]
Chr5:139931764 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.3(SRA1):c.5C>G (p.Thr2Arg) single nucleotide variant Inborn genetic diseases [RCV002688145] Chr5:140557484 [GRCh38]
Chr5:139937069 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.135G>T (p.Gln45His) single nucleotide variant Inborn genetic diseases [RCV002733382] Chr5:140557163 [GRCh38]
Chr5:139936748 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.238A>C (p.Ser80Arg) single nucleotide variant not provided [RCV002797318] Chr5:140552098 [GRCh38]
Chr5:139931683 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.514A>G (p.Met172Val) single nucleotide variant Inborn genetic diseases [RCV002693515] Chr5:140550861 [GRCh38]
Chr5:139930446 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.183C>G (p.Pro61=) single nucleotide variant not provided [RCV003079899] Chr5:140552153 [GRCh38]
Chr5:139931738 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.572C>T (p.Ala191Val) single nucleotide variant Inborn genetic diseases [RCV002799200] Chr5:140550803 [GRCh38]
Chr5:139930388 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.350C>A (p.Thr117Lys) single nucleotide variant Inborn genetic diseases [RCV002742109] Chr5:140551986 [GRCh38]
Chr5:139931571 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.181C>T (p.Pro61Ser) single nucleotide variant Inborn genetic diseases [RCV002983744] Chr5:140552155 [GRCh38]
Chr5:139931740 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.123C>T (p.Val41=) single nucleotide variant not provided [RCV002928293] Chr5:140557175 [GRCh38]
Chr5:139936760 [GRCh37]
Chr5:5q31.3
benign
NM_001035235.4(SRA1):c.194C>G (p.Pro65Arg) single nucleotide variant Inborn genetic diseases [RCV002853795] Chr5:140552142 [GRCh38]
Chr5:139931727 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.383G>C (p.Arg128Pro) single nucleotide variant Inborn genetic diseases [RCV002803764] Chr5:140551141 [GRCh38]
Chr5:139930726 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.-18G>A single nucleotide variant Inborn genetic diseases [RCV002961058] Chr5:140557470 [GRCh38]
Chr5:139937055 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.23C>T (p.Pro8Leu) single nucleotide variant not provided [RCV003060015] Chr5:140557430 [GRCh38]
Chr5:139937015 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.279C>T (p.Val93=) single nucleotide variant not provided [RCV002582415] Chr5:140552057 [GRCh38]
Chr5:139931642 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.25+9A>G single nucleotide variant not provided [RCV002635436] Chr5:140557419 [GRCh38]
Chr5:139937004 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.564A>G (p.Arg188=) single nucleotide variant not provided [RCV002611938] Chr5:140550811 [GRCh38]
Chr5:139930396 [GRCh37]
Chr5:5q31.3
likely benign
NM_001035235.4(SRA1):c.134A>T (p.Gln45Leu) single nucleotide variant Inborn genetic diseases [RCV003202379] Chr5:140557164 [GRCh38]
Chr5:139936749 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.506G>A (p.Arg169His) single nucleotide variant Inborn genetic diseases [RCV003218612] Chr5:140550869 [GRCh38]
Chr5:139930454 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.269G>C (p.Ser90Thr) single nucleotide variant Inborn genetic diseases [RCV003264461] Chr5:140552067 [GRCh38]
Chr5:139931652 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_001035235.4(SRA1):c.28A>G (p.Asn10Asp) single nucleotide variant Inborn genetic diseases [RCV003356856] Chr5:140557270 [GRCh38]
Chr5:139936855 [GRCh37]
Chr5:5q31.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1393
Count of miRNA genes:623
Interacting mature miRNAs:733
Transcripts:ENST00000336283, ENST00000520427, ENST00000523259, ENST00000602657, ENST00000602775, ENST00000602875
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.

Markers in Region
RH122995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,930,624 - 139,930,956UniSTSGRCh37
Build 365139,910,808 - 139,911,140RGDNCBI36
Celera5136,007,375 - 136,007,707RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,963 - 135,076,295UniSTS
TNG Radiation Hybrid Map564170.0UniSTS
D5S2251E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,938,087 - 139,938,210UniSTSGRCh37
Build 365139,918,271 - 139,918,394RGDNCBI36
Celera5136,014,837 - 136,014,960RGD
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map5q31UniSTS
HuRef5135,083,424 - 135,083,547UniSTS
D5S2258E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,930,194 - 139,930,319UniSTSGRCh37
Build 365139,910,378 - 139,910,503RGDNCBI36
Celera5136,006,945 - 136,007,070RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,533 - 135,075,658UniSTS
SHGC-132909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,929,729 - 139,930,001UniSTSGRCh37
Build 365139,909,913 - 139,910,185RGDNCBI36
Celera5136,006,480 - 136,006,752RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,068 - 135,075,340UniSTS
TNG Radiation Hybrid Map564170.0UniSTS
SGC30750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,930,097 - 139,930,221UniSTSGRCh37
Build 365139,910,281 - 139,910,405RGDNCBI36
Celera5136,006,848 - 136,006,972RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,436 - 135,075,560UniSTS
GeneMap99-GB4 RH Map5531.42UniSTS
Whitehead-RH Map5441.7UniSTS
NCBI RH Map5889.1UniSTS
PMC170950P4  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,930,308 - 139,930,675UniSTSGRCh37
Build 365139,910,492 - 139,910,859RGDNCBI36
Celera5136,007,059 - 136,007,426RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,647 - 135,076,014UniSTS
APBB3_9088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,937,691 - 139,938,406UniSTSGRCh37
Build 365139,917,875 - 139,918,590RGDNCBI36
Celera5136,014,441 - 136,015,156RGD
HuRef5135,083,028 - 135,083,743UniSTS
SHGC-56860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,929,875 - 139,930,027UniSTSGRCh37
Build 365139,910,059 - 139,910,211RGDNCBI36
Celera5136,006,626 - 136,006,778RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,214 - 135,075,366UniSTS
A007D18  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,937,883 - 139,938,133UniSTSGRCh37
Build 365139,918,067 - 139,918,317RGDNCBI36
Celera5136,014,633 - 136,014,883RGD
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map5q31UniSTS
HuRef5135,083,220 - 135,083,470UniSTS
GeneMap99-GB4 RH Map5531.62UniSTS
NCBI RH Map5889.1UniSTS
RH16024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,937,995 - 139,938,155UniSTSGRCh37
Build 365139,918,179 - 139,918,339RGDNCBI36
Celera5136,014,745 - 136,014,905RGD
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map5q31UniSTS
HuRef5135,083,332 - 135,083,492UniSTS
GeneMap99-GB4 RH Map5531.62UniSTS
NCBI RH Map5889.1UniSTS
RH45891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375139,929,671 - 139,929,838UniSTSGRCh37
Build 365139,909,855 - 139,910,022RGDNCBI36
Celera5136,006,422 - 136,006,589RGD
Cytogenetic Map5q31.3UniSTS
HuRef5135,075,010 - 135,075,177UniSTS
GeneMap99-GB4 RH Map5531.22UniSTS
NCBI RH Map5889.1UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2423 2829 1713 613 1924 455 4353 2070 3442 410 1448 1607 171 1204 2786 4
Low 9 156 10 10 26 10 2 124 279 9 1 2 2 1
Below cutoff 1 3 3 1 11 6 3 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_031847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001035235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001253764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_045586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_045587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC011399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF092038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF293024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF293025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF293026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF318361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI140060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054960 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC040043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC067895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ052761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU553214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX165918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA311407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ286291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MT500689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MT500690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000336283   ⟹   ENSP00000337513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,550,068 - 140,557,473 (-)Ensembl
RefSeq Acc Id: ENST00000520427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,550,682 - 140,557,677 (-)Ensembl
RefSeq Acc Id: ENST00000523259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,550,534 - 140,557,446 (-)Ensembl
RefSeq Acc Id: ENST00000602657   ⟹   ENSP00000473378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,537,340 - 140,551,128 (-)Ensembl
RefSeq Acc Id: ENST00000602775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,550,068 - 140,557,456 (-)Ensembl
RefSeq Acc Id: ENST00000602875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,550,552 - 140,557,446 (-)Ensembl
RefSeq Acc Id: NM_001035235   ⟹   NP_001030312
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,550,068 - 140,557,473 (-)NCBI
GRCh375139,929,652 - 139,937,678 (-)NCBI
Build 365139,909,837 - 139,917,862 (-)NCBI Archive
HuRef5135,074,991 - 135,083,015 (-)NCBI
CHM1_15139,362,900 - 139,370,926 (-)NCBI
T2T-CHM13v2.05141,075,498 - 141,082,904 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001253764   ⟹   NP_001240693
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,550,068 - 140,557,473 (-)NCBI
GRCh375139,929,652 - 139,937,678 (-)NCBI
HuRef5135,074,991 - 135,083,015 (-)NCBI
CHM1_15139,362,900 - 139,370,289 (-)NCBI
T2T-CHM13v2.05141,075,498 - 141,082,904 (-)NCBI
Sequence:
RefSeq Acc Id: NR_045586
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,550,067 - 140,558,093 (-)NCBI
GRCh375139,929,652 - 139,937,678 (-)NCBI
HuRef5135,074,991 - 135,083,015 (-)NCBI
CHM1_15139,362,900 - 139,370,926 (-)NCBI
T2T-CHM13v2.05141,075,497 - 141,083,524 (-)NCBI
Sequence:
RefSeq Acc Id: NR_045587
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,550,068 - 140,557,473 (-)NCBI
GRCh375139,929,652 - 139,937,678 (-)NCBI
HuRef5135,074,991 - 135,083,015 (-)NCBI
CHM1_15139,362,900 - 139,370,289 (-)NCBI
T2T-CHM13v2.05141,075,498 - 141,082,904 (-)NCBI
Sequence:
RefSeq Acc Id: NP_001030312   ⟸   NM_001035235
- Peptide Label: isoform 1
- UniProtKB: Q9HD15 (UniProtKB/Swiss-Prot),   Q9HD13 (UniProtKB/Swiss-Prot),   Q8IXM1 (UniProtKB/Swiss-Prot),   Q6NVU9 (UniProtKB/Swiss-Prot),   Q9HD14 (UniProtKB/Swiss-Prot),   B3KNT3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001240693   ⟸   NM_001253764
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: ENSP00000337513   ⟸   ENST00000336283
RefSeq Acc Id: ENSP00000473378   ⟸   ENST00000602657
Protein Domains
SRA1/Sec31

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9HD15-F1-model_v2 AlphaFold Q9HD15 1-224 view protein structure

Promoters
RGD ID:6803582
Promoter ID:HG_KWN:51277
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:NM_001035235,   UC003LFZ.1,   UC010JFM.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365139,917,176 - 139,918,082 (-)MPROMDB
RGD ID:6870818
Promoter ID:EPDNEW_H8574
Type:initiation region
Name:SRA1_1
Description:steroid receptor RNA activator 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,557,456 - 140,557,516EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11281 AgrOrtholog
COSMIC SRA1 COSMIC
Ensembl Genes ENSG00000213523 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000336283 ENTREZGENE
  ENST00000336283.9 UniProtKB/Swiss-Prot
  ENST00000602657.1 UniProtKB/TrEMBL
  ENST00000602775 ENTREZGENE
Gene3D-CATH Functional domain of the splicing factor Prp18 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000213523 GTEx
HGNC ID HGNC:11281 ENTREZGENE
Human Proteome Map SRA1 Human Proteome Map
InterPro SRA1-protein/COPII_Sec31 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Steroid_recept_RNA_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10011 UniProtKB/Swiss-Prot
NCBI Gene 10011 ENTREZGENE
OMIM 603819 OMIM
PANTHER PTHR18834 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STEROID RECEPTOR RNA ACTIVATOR 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam SRA1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36110 PharmGKB
UniProt B3KNT3 ENTREZGENE, UniProtKB/TrEMBL
  Q6NVU9 ENTREZGENE
  Q8IXM1 ENTREZGENE
  Q9HD13 ENTREZGENE
  Q9HD14 ENTREZGENE
  Q9HD15 ENTREZGENE
  R4GMW4_HUMAN UniProtKB/TrEMBL
  SRA1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q6NVU9 UniProtKB/Swiss-Prot
  Q8IXM1 UniProtKB/Swiss-Prot
  Q9HD13 UniProtKB/Swiss-Prot
  Q9HD14 UniProtKB/Swiss-Prot