STARD3NL (STARD3 N-terminal like) - Rat Genome Database

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Gene: STARD3NL (STARD3 N-terminal like) Homo sapiens
Analyze
Symbol: STARD3NL
Name: STARD3 N-terminal like
RGD ID: 1318520
HGNC Page HGNC:19169
Description: Enables cholesterol binding activity and protein homodimerization activity. Involved in vesicle tethering to endoplasmic reticulum. Located in endoplasmic reticulum membrane; endoplasmic reticulum-endosome membrane contact site; and late endosome membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MENTHO; MGC3251; MLN64 N-terminal domain homolog; STARD3 N-terminal-like protein
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
GRCh38738,178,245 - 38,230,669 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl738,178,245 - 38,230,670 (+)EnsemblGRCh38hg38GRCh38
GRCh37738,217,847 - 38,270,270 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36738,184,458 - 38,236,795 (+)NCBINCBI36Build 36hg18NCBI36
Build 34737,991,172 - 38,043,509NCBI
Celera738,202,354 - 38,254,700 (+)NCBICelera
Cytogenetic Map7p14.1NCBI
HuRef738,098,656 - 38,151,174 (+)NCBIHuRef
CHM1_1738,217,726 - 38,270,163 (+)NCBICHM1_1
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2738,255,486 - 38,307,952 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

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. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9847074   PMID:12393907   PMID:12477932   PMID:12690205   PMID:12853948   PMID:12975309   PMID:14702039   PMID:15489334   PMID:15718238   PMID:16344560   PMID:16709157   PMID:17081983  
PMID:17213182   PMID:17897319   PMID:18187620   PMID:18636124   PMID:19322201   PMID:19801982   PMID:19913121   PMID:19946888   PMID:20628086   PMID:20881960   PMID:21873635   PMID:21988832  
PMID:22310353   PMID:22504420   PMID:24105263   PMID:25429064   PMID:27068960   PMID:27173435   PMID:28298427   PMID:29858488   PMID:31536960   PMID:32296183   PMID:33845483   PMID:33961781  
PMID:35098646   PMID:35271311   PMID:37314216  


Genomics

Comparative Map Data
STARD3NL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38738,178,245 - 38,230,669 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl738,178,245 - 38,230,670 (+)EnsemblGRCh38hg38GRCh38
GRCh37738,217,847 - 38,270,270 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36738,184,458 - 38,236,795 (+)NCBINCBI36Build 36hg18NCBI36
Build 34737,991,172 - 38,043,509NCBI
Celera738,202,354 - 38,254,700 (+)NCBICelera
Cytogenetic Map7p14.1NCBI
HuRef738,098,656 - 38,151,174 (+)NCBIHuRef
CHM1_1738,217,726 - 38,270,163 (+)NCBICHM1_1
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2738,255,486 - 38,307,952 (+)NCBI
Stard3nl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391319,541,846 - 19,579,983 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1319,541,846 - 19,579,965 (-)EnsemblGRCm39 Ensembl
GRCm381319,357,676 - 19,395,813 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1319,357,676 - 19,395,795 (-)EnsemblGRCm38mm10GRCm38
MGSCv371319,449,545 - 19,487,621 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361319,365,141 - 19,403,217 (-)NCBIMGSCv36mm8
Celera1319,660,880 - 19,698,789 (-)NCBICelera
Cytogenetic Map13A2NCBI
cM Map136.89NCBI
Stard3nl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81750,278,859 - 50,312,864 (+)NCBIGRCr8
mRatBN7.21745,583,278 - 45,617,226 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1745,583,266 - 45,617,226 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1747,655,768 - 47,689,740 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01752,414,916 - 52,448,894 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01746,905,109 - 46,939,250 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01747,662,553 - 47,696,453 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1747,662,532 - 47,696,444 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01755,791,548 - 55,825,467 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41753,402,078 - 53,436,085 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11753,404,918 - 53,438,922 (+)NCBI
Celera1750,916,749 - 50,950,697 (-)NCBICelera
Cytogenetic Map17q11NCBI
Stard3nl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554605,364,552 - 5,423,381 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554605,364,546 - 5,423,330 (-)NCBIChiLan1.0ChiLan1.0
STARD3NL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2643,006,418 - 43,058,868 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1791,331,146 - 91,383,603 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0738,811,588 - 38,864,042 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1739,032,317 - 39,084,789 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl739,032,337 - 39,084,789 (+)Ensemblpanpan1.1panPan2
STARD3NL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11811,732,949 - 11,784,241 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1811,733,368 - 11,784,248 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1811,374,886 - 11,426,155 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01812,001,590 - 12,052,988 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1812,001,856 - 12,052,993 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11811,812,882 - 11,870,386 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01811,735,126 - 11,790,958 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01811,966,769 - 12,018,062 (-)NCBIUU_Cfam_GSD_1.0
Stard3nl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511894,278,020 - 94,325,639 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647813,489,691 - 13,537,579 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647813,489,743 - 13,537,225 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
STARD3NL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9108,631,256 - 108,676,183 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19108,631,239 - 108,675,617 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29119,542,645 - 119,577,352 (+)NCBISscrofa10.2Sscrofa10.2susScr3
STARD3NL
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12120,276,861 - 20,329,340 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2120,278,679 - 20,329,295 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660622,014,032 - 2,066,530 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Stard3nl
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474023,063,504 - 23,099,087 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474023,063,906 - 23,098,411 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in STARD3NL
9 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 copy number gain See cases [RCV000051159] Chr7:54185..41875885 [GRCh38]
Chr7:54185..41915483 [GRCh37]
Chr7:149268..41882008 [NCBI36]
Chr7:7p22.3-14.1
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3 copy number gain See cases [RCV000053532] Chr7:33328312..62377476 [GRCh38]
Chr7:33367924..61831899 [GRCh37]
Chr7:33334449..61469334 [NCBI36]
Chr7:7p14.3-q11.21
pathogenic
NM_032016.3(STARD3NL):c.319C>T (p.Arg107Ter) single nucleotide variant Malignant melanoma [RCV000067870] Chr7:38215043 [GRCh38]
Chr7:38254644 [GRCh37]
Chr7:38221169 [NCBI36]
Chr7:7p14.1
not provided
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p14.1-12.3(chr7:37303478-48660738)x1 copy number loss See cases [RCV000137139] Chr7:37303478..48660738 [GRCh38]
Chr7:37343082..48700334 [GRCh37]
Chr7:37309607..48670880 [NCBI36]
Chr7:7p14.1-12.3
pathogenic
GRCh38/hg38 7p14.2-14.1(chr7:35460776-42013800)x1 copy number loss See cases [RCV000138190] Chr7:35460776..42013800 [GRCh38]
Chr7:35500386..42053399 [GRCh37]
Chr7:35466911..42019924 [NCBI36]
Chr7:7p14.2-14.1
pathogenic
GRCh38/hg38 7p14.3-14.1(chr7:32678391-41044983)x1 copy number loss See cases [RCV000140283] Chr7:32678391..41044983 [GRCh38]
Chr7:32718003..41084581 [GRCh37]
Chr7:32684528..41051106 [NCBI36]
Chr7:7p14.3-14.1
pathogenic
GRCh38/hg38 7p14.1(chr7:38208739-38687927)x3 copy number gain See cases [RCV000140885] Chr7:38208739..38687927 [GRCh38]
Chr7:38248340..38727527 [GRCh37]
Chr7:38214865..38694052 [NCBI36]
Chr7:7p14.1
likely benign|uncertain significance
GRCh38/hg38 7p14.1-13(chr7:38177999-45304100)x1 copy number loss See cases [RCV000142297] Chr7:38177999..45304100 [GRCh38]
Chr7:38217601..45343699 [GRCh37]
Chr7:38184126..45310224 [NCBI36]
Chr7:7p14.1-13
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p14.3-13(chr7:32911003-44576005)x1 copy number loss See cases [RCV000446955] Chr7:32911003..44576005 [GRCh37]
Chr7:7p14.3-13
pathogenic
GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3 copy number gain See cases [RCV000512091] Chr7:11048840..52863626 [GRCh37]
Chr7:7p21.3-12.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p14.1(chr7:38209836-38295997)x1 copy number loss not provided [RCV000682780] Chr7:38209836..38295997 [GRCh37]
Chr7:7p14.1
uncertain significance
GRCh37/hg19 7p14.3-13(chr7:30463886-43470805)x3 copy number gain not provided [RCV000682909] Chr7:30463886..43470805 [GRCh37]
Chr7:7p14.3-13
pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p14.1(chr7:37213108-40255122)x3 copy number gain not provided [RCV000746632] Chr7:37213108..40255122 [GRCh37]
Chr7:7p14.1
pathogenic
GRCh37/hg19 7p14.1(chr7:38043677-38501065)x1 copy number loss not provided [RCV000746635] Chr7:38043677..38501065 [GRCh37]
Chr7:7p14.1
benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p14.1(chr7:37202606-39500521)x3 copy number gain not provided [RCV001005935] Chr7:37202606..39500521 [GRCh37]
Chr7:7p14.1
uncertain significance
GRCh37/hg19 7p15.2-14.1(chr7:27507832-39072473) copy number gain not specified [RCV002053677] Chr7:27507832..39072473 [GRCh37]
Chr7:7p15.2-14.1
likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3
uncertain significance
NM_032016.4(STARD3NL):c.662C>A (p.Ala221Asp) single nucleotide variant not specified [RCV004159067] Chr7:38228811 [GRCh38]
Chr7:38268412 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_032016.4(STARD3NL):c.122A>T (p.Glu41Val) single nucleotide variant not specified [RCV004306716] Chr7:38207626 [GRCh38]
Chr7:38247227 [GRCh37]
Chr7:7p14.1
uncertain significance
GRCh37/hg19 7p14.3-14.1(chr7:33478398-39686397)x1 copy number loss not specified [RCV003986710] Chr7:33478398..39686397 [GRCh37]
Chr7:7p14.3-14.1
likely pathogenic
NM_032016.4(STARD3NL):c.241G>C (p.Glu81Gln) single nucleotide variant not specified [RCV004463377] Chr7:38214372 [GRCh38]
Chr7:38253973 [GRCh37]
Chr7:7p14.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1402
Count of miRNA genes:550
Interacting mature miRNAs:600
Transcripts:ENST00000009041, ENST00000396013, ENST00000429075, ENST00000434197, ENST00000440144, ENST00000453225, ENST00000471550, ENST00000544203
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1558711BP56_HBlood pressure QTL 56 (human)2.240.000002Blood pressuresystolic73634937162349371Human
597266585GWAS1362659_Hhigh density lipoprotein cholesterol measurement QTL GWAS1362659 (human)3e-22high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)73822557838225579Human
597123442GWAS1219516_Hblood protein measurement QTL GWAS1219516 (human)5e-12blood protein amount (VT:0005416)blood protein measurement (CMO:0000028)73820256538202566Human
597144497GWAS1240571_HCOVID-19 QTL GWAS1240571 (human)0.0000004COVID-1973820273038202731Human
406959046GWAS608022_Hresponse to xenobiotic stimulus QTL GWAS608022 (human)0.000006response to xenobiotic stimulus73820130738201308Human
1559132SAPOB3_HSerum apolipoprotein B level QTL 3 (human)20.4Apolipoprotein levelapolipoprotein B73289107458891074Human
597172883GWAS1268957_Hthrombopoietin measurement QTL GWAS1268957 (human)6e-14thrombopoietin measurement73819360138193602Human
2289453BW297_HBody weight QTL 297 (human)3.83Body weightbody mass index72334946449349464Human
597274349GWAS1370423_Hhigh density lipoprotein cholesterol measurement QTL GWAS1370423 (human)9e-12high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)73822557838225579Human
597279662GWAS1375736_Hhigh density lipoprotein cholesterol measurement QTL GWAS1375736 (human)9e-13high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)73822557838225579Human
597064267GWAS1160341_Hmosquito bite reaction size measurement QTL GWAS1160341 (human)0.000009mosquito bite reaction size measurement73818215238182153Human
597356647GWAS1452721_Hbody height QTL GWAS1452721 (human)1e-29body height (VT:0001253)body height (CMO:0000106)73822232038222321Human
2302781MAMTS16_HMammary tumor susceptibility QTL 16 (human)0.033Mammary tumor susceptibility73634937162349371Human

Markers in Region
D7S2497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37738,261,658 - 38,261,859UniSTSGRCh37
GRCh37738,261,504 - 38,261,698UniSTSGRCh37
Build 36738,228,183 - 38,228,384RGDNCBI36
Celera738,246,080 - 38,246,281RGD
Celera738,245,926 - 38,246,120UniSTS
Cytogenetic Map7p14-p13UniSTS
HuRef738,142,398 - 38,142,592UniSTS
HuRef738,142,552 - 38,142,753UniSTS
CRA_TCAGchr7v2738,299,176 - 38,299,370UniSTS
CRA_TCAGchr7v2738,299,330 - 38,299,531UniSTS
Marshfield Genetic Map758.86RGD
Genethon Genetic Map760.0UniSTS
TNG Radiation Hybrid Map718747.0UniSTS
deCODE Assembly Map759.59UniSTS
Whitehead-YAC Contig Map7 UniSTS
GeneMap99-G3 RH Map71642.0UniSTS
RH80173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37738,257,579 - 38,257,819UniSTSGRCh37
Build 36738,224,104 - 38,224,344RGDNCBI36
Celera738,242,003 - 38,242,243RGD
Cytogenetic Map7p14-p13UniSTS
HuRef738,138,473 - 38,138,713UniSTS
CRA_TCAGchr7v2738,295,261 - 38,295,501UniSTS
SHGC-172109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37738,219,366 - 38,219,650UniSTSGRCh37
Build 36738,185,891 - 38,186,175RGDNCBI36
Celera738,203,788 - 38,204,072RGD
Cytogenetic Map7p14-p13UniSTS
HuRef738,100,215 - 38,100,499UniSTS
CRA_TCAGchr7v2738,257,045 - 38,257,329UniSTS
TNG Radiation Hybrid Map718737.0UniSTS
HSC205_(7Gr378mb)  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37738,256,029 - 38,256,155UniSTSGRCh37
Build 36738,222,554 - 38,222,680RGDNCBI36
Celera738,240,453 - 38,240,579RGD
Cytogenetic Map7p14-p13UniSTS
HuRef738,136,923 - 38,137,049UniSTS
CRA_TCAGchr7v2738,293,711 - 38,293,837UniSTS
STS-F09950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37738,269,703 - 38,269,796UniSTSGRCh37
Build 36738,236,228 - 38,236,321RGDNCBI36
Celera738,254,133 - 38,254,226RGD
Cytogenetic Map7p14-p13UniSTS
HuRef738,150,605 - 38,150,698UniSTS
CRA_TCAGchr7v2738,307,383 - 38,307,476UniSTS
GeneMap99-GB4 RH Map7172.43UniSTS
NCBI RH Map7576.1UniSTS
D7S2497  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7p14-p13UniSTS
Marshfield Genetic Map758.86UniSTS
Genethon Genetic Map760.0UniSTS
TNG Radiation Hybrid Map718747.0UniSTS
deCODE Assembly Map759.59UniSTS
Whitehead-YAC Contig Map7 UniSTS
GeneMap99-G3 RH Map71642.0UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2437 2788 2253 4974 1726 2350 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1616 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_030015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363340 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011515572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC093460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC244625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI289220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ492267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ716734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS101346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA131127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA258701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DT218211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X85793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000009041   ⟹   ENSP00000009041
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,245 - 38,230,669 (+)Ensembl
Ensembl Acc Id: ENST00000396013   ⟹   ENSP00000379334
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,351 - 38,230,381 (+)Ensembl
Ensembl Acc Id: ENST00000429075   ⟹   ENSP00000402028
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,395 - 38,219,629 (+)Ensembl
Ensembl Acc Id: ENST00000434197   ⟹   ENSP00000394000
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,263 - 38,230,379 (+)Ensembl
Ensembl Acc Id: ENST00000440144   ⟹   ENSP00000411933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,376 - 38,217,305 (+)Ensembl
Ensembl Acc Id: ENST00000453225   ⟹   ENSP00000395455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,390 - 38,217,269 (+)Ensembl
Ensembl Acc Id: ENST00000471550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl738,178,324 - 38,230,670 (+)Ensembl
RefSeq Acc Id: NM_001363339   ⟹   NP_001350268
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363340   ⟹   NP_001350269
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363343   ⟹   NP_001350272
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363344   ⟹   NP_001350273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363345   ⟹   NP_001350274
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363346   ⟹   NP_001350275
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363347   ⟹   NP_001350276
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
Sequence:
RefSeq Acc Id: NM_032016   ⟹   NP_114405
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,230,669 (+)NCBI
GRCh37738,217,808 - 38,270,272 (+)NCBI
Build 36738,184,458 - 38,236,795 (+)NCBI Archive
Celera738,202,354 - 38,254,700 (+)RGD
HuRef738,098,656 - 38,151,174 (+)NCBI
CHM1_1738,217,726 - 38,270,163 (+)NCBI
T2T-CHM13v2.0738,319,177 - 38,371,581 (+)NCBI
CRA_TCAGchr7v2738,255,486 - 38,307,952 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011515572   ⟹   XP_011513874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,198,214 - 38,230,669 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012693   ⟹   XP_016868182
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,198,216 - 38,230,669 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024446955   ⟹   XP_024302723
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,201,714 - 38,230,669 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047420920   ⟹   XP_047276876
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,198,216 - 38,230,669 (+)NCBI
RefSeq Acc Id: XM_047420921   ⟹   XP_047276877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,198,214 - 38,230,669 (+)NCBI
RefSeq Acc Id: XM_054359170   ⟹   XP_054215145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,339,158 - 38,371,581 (+)NCBI
RefSeq Acc Id: XM_054359171   ⟹   XP_054215146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,339,158 - 38,371,581 (+)NCBI
RefSeq Acc Id: XM_054359172   ⟹   XP_054215147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,342,657 - 38,371,581 (+)NCBI
RefSeq Acc Id: XM_054359173   ⟹   XP_054215148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,342,662 - 38,371,581 (+)NCBI
RefSeq Acc Id: XM_054359174   ⟹   XP_054215149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,339,156 - 38,371,581 (+)NCBI
RefSeq Acc Id: XM_054359175   ⟹   XP_054215150
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0738,339,156 - 38,371,581 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001350268 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350269 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350272 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350273 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350274 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350275 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350276 (Get FASTA)   NCBI Sequence Viewer  
  NP_114405 (Get FASTA)   NCBI Sequence Viewer  
  XP_011513874 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868182 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302723 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276876 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276877 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215145 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215146 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215147 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215148 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215149 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215150 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH03074 (Get FASTA)   NCBI Sequence Viewer  
  AAH05959 (Get FASTA)   NCBI Sequence Viewer  
  AAQ89008 (Get FASTA)   NCBI Sequence Viewer  
  AAS07552 (Get FASTA)   NCBI Sequence Viewer  
  BAG37796 (Get FASTA)   NCBI Sequence Viewer  
  CAA59792 (Get FASTA)   NCBI Sequence Viewer  
  CAD37353 (Get FASTA)   NCBI Sequence Viewer  
  CAJ00716 (Get FASTA)   NCBI Sequence Viewer  
  EAL23983 (Get FASTA)   NCBI Sequence Viewer  
  EAW94088 (Get FASTA)   NCBI Sequence Viewer  
  EAW94089 (Get FASTA)   NCBI Sequence Viewer  
  EAW94090 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000009041
  ENSP00000009041.7
  ENSP00000379334
  ENSP00000379334.1
  ENSP00000394000
  ENSP00000394000.1
  ENSP00000395455.1
  ENSP00000402028
  ENSP00000402028.1
  ENSP00000411933.1
GenBank Protein O95772 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_114405   ⟸   NM_032016
- Peptide Label: isoform 1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011513874   ⟸   XM_011515572
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868182   ⟸   XM_017012693
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302723   ⟸   XM_024446955
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001350269   ⟸   NM_001363340
- Peptide Label: isoform 1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350273   ⟸   NM_001363344
- Peptide Label: isoform 2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350275   ⟸   NM_001363346
- Peptide Label: isoform 2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350268   ⟸   NM_001363339
- Peptide Label: isoform 1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350272   ⟸   NM_001363343
- Peptide Label: isoform 2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350276   ⟸   NM_001363347
- Peptide Label: isoform 2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350274   ⟸   NM_001363345
- Peptide Label: isoform 2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000395455   ⟸   ENST00000453225
Ensembl Acc Id: ENSP00000402028   ⟸   ENST00000429075
Ensembl Acc Id: ENSP00000411933   ⟸   ENST00000440144
Ensembl Acc Id: ENSP00000009041   ⟸   ENST00000009041
Ensembl Acc Id: ENSP00000394000   ⟸   ENST00000434197
Ensembl Acc Id: ENSP00000379334   ⟸   ENST00000396013
RefSeq Acc Id: XP_047276877   ⟸   XM_047420921
- Peptide Label: isoform X2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047276876   ⟸   XM_047420920
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215149   ⟸   XM_054359174
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215150   ⟸   XM_054359175
- Peptide Label: isoform X2
- UniProtKB: C9JKL2 (UniProtKB/TrEMBL),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215146   ⟸   XM_054359171
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215145   ⟸   XM_054359170
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215147   ⟸   XM_054359172
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054215148   ⟸   XM_054359173
- Peptide Label: isoform X1
- UniProtKB: O95772 (UniProtKB/Swiss-Prot),   A4D1X0 (UniProtKB/Swiss-Prot),   C9JPX5 (UniProtKB/TrEMBL)
Protein Domains
MENTAL

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O95772-F1-model_v2 AlphaFold O95772 1-234 view protein structure

Promoters
RGD ID:7210403
Promoter ID:EPDNEW_H10948
Type:initiation region
Name:STARD3NL_1
Description:STARD3 N-terminal like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10949  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,245 - 38,178,305EPDNEW
RGD ID:7210405
Promoter ID:EPDNEW_H10949
Type:initiation region
Name:STARD3NL_2
Description:STARD3 N-terminal like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10948  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38738,178,348 - 38,178,408EPDNEW
RGD ID:6806238
Promoter ID:HG_KWN:57050
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:OTTHUMT00000226929,   OTTHUMT00000338402,   OTTHUMT00000338403,   OTTHUMT00000338404,   OTTHUMT00000338405,   UC003TFS.1,   UC003TFT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36738,184,054 - 38,184,554 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19169 AgrOrtholog
COSMIC STARD3NL COSMIC
Ensembl Genes ENSG00000010270 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000009041 ENTREZGENE
  ENST00000009041.12 UniProtKB/Swiss-Prot
  ENST00000396013 ENTREZGENE
  ENST00000396013.5 UniProtKB/Swiss-Prot
  ENST00000429075 ENTREZGENE
  ENST00000429075.1 UniProtKB/TrEMBL
  ENST00000434197 ENTREZGENE
  ENST00000434197.5 UniProtKB/TrEMBL
  ENST00000440144.5 UniProtKB/TrEMBL
  ENST00000453225.5 UniProtKB/TrEMBL
GTEx ENSG00000010270 GTEx
HGNC ID HGNC:19169 ENTREZGENE
Human Proteome Map STARD3NL Human Proteome Map
InterPro MENTAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STARD3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:83930 UniProtKB/Swiss-Prot
NCBI Gene 83930 ENTREZGENE
OMIM 611759 OMIM
PANTHER STARD3 N-TERMINAL-LIKE PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STEROIDOGENIC ACUTE REGULATORY PROTEIN-LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MENTAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134990065 PharmGKB
PROSITE MENTAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A4D1X0 ENTREZGENE
  C9J3F5_HUMAN UniProtKB/TrEMBL
  C9JJ39_HUMAN UniProtKB/TrEMBL
  C9JKL2 ENTREZGENE, UniProtKB/TrEMBL
  C9JPX5 ENTREZGENE, UniProtKB/TrEMBL
  O95772 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A4D1X0 UniProtKB/Swiss-Prot