SLC37A3 (solute carrier family 37 member 3) - Rat Genome Database

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Gene: SLC37A3 (solute carrier family 37 member 3) Homo sapiens
Analyze
Symbol: SLC37A3
Name: solute carrier family 37 member 3
RGD ID: 1321198
HGNC Page HGNC:20651
Description: Enables xenobiotic transmembrane transporter activity. Involved in xenobiotic transmembrane transport. Located in endoplasmic reticulum membrane and lysosomal membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ16367; MGC32939; solute carrier family 37 (glycerol-3-phosphate transporter), member 3; solute carrier family 37, member 3; SPX3; sugar phosphate exchanger 3; sugar-phosphate exchange protein 3
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
GRCh387140,333,752 - 140,398,530 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7140,293,693 - 140,404,433 (-)EnsemblGRCh38hg38GRCh38
GRCh377140,033,552 - 140,098,330 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367139,680,021 - 139,744,780 (-)NCBINCBI36Build 36hg18NCBI36
Celera7134,755,301 - 134,820,377 (-)NCBICelera
Cytogenetic Map7q34NCBI
HuRef7134,326,585 - 134,391,017 (-)NCBIHuRef
CHM1_17139,968,423 - 140,033,217 (-)NCBICHM1_1
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27139,362,371 - 139,427,142 (-)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. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:9847074   PMID:11230166   PMID:12477932   PMID:12690205   PMID:12811562   PMID:15146197   PMID:16344560   PMID:21752829   PMID:21873635   PMID:21949678   PMID:21988832  
PMID:28514442   PMID:29745899   PMID:31343991   PMID:33961781   PMID:35748872  


Genomics

Comparative Map Data
SLC37A3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387140,333,752 - 140,398,530 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7140,293,693 - 140,404,433 (-)EnsemblGRCh38hg38GRCh38
GRCh377140,033,552 - 140,098,330 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367139,680,021 - 139,744,780 (-)NCBINCBI36Build 36hg18NCBI36
Celera7134,755,301 - 134,820,377 (-)NCBICelera
Cytogenetic Map7q34NCBI
HuRef7134,326,585 - 134,391,017 (-)NCBIHuRef
CHM1_17139,968,423 - 140,033,217 (-)NCBICHM1_1
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27139,362,371 - 139,427,142 (-)NCBI
Slc37a3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39639,311,704 - 39,354,659 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl639,311,707 - 39,354,609 (-)EnsemblGRCm39 Ensembl
GRCm38639,334,770 - 39,377,725 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl639,334,773 - 39,377,675 (-)EnsemblGRCm38mm10GRCm38
MGSCv37639,284,769 - 39,327,706 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36639,265,592 - 39,307,251 (-)NCBIMGSCv36mm8
Celera639,320,062 - 39,362,925 (-)NCBICelera
Cytogenetic Map6B1NCBI
cM Map618.11NCBI
Slc37a3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8469,076,124 - 69,120,392 (-)NCBIGRCr8
mRatBN7.2468,109,314 - 68,153,590 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl468,081,939 - 68,153,568 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx473,031,070 - 73,076,773 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0468,952,204 - 68,997,906 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0467,360,319 - 67,403,020 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0467,118,918 - 67,162,821 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl467,118,910 - 67,162,808 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0466,925,988 - 66,969,270 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4466,840,635 - 66,885,849 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1467,118,168 - 67,161,943 (-)NCBI
Celera463,115,904 - 63,159,080 (-)NCBICelera
Cytogenetic Map4q23NCBI
Slc37a3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554942,858,727 - 2,934,014 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554942,891,415 - 2,933,067 (+)NCBIChiLan1.0ChiLan1.0
SLC37A3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26177,088,724 - 177,193,930 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1729,102,005 - 29,204,198 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07132,236,350 - 132,338,150 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17144,717,312 - 144,815,870 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7144,755,561 - 144,815,491 (-)Ensemblpanpan1.1panPan2
SLC37A3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1168,574,973 - 8,615,961 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl168,575,001 - 8,615,971 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha169,410,259 - 9,461,381 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0168,487,307 - 8,538,224 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl168,487,345 - 8,538,222 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1168,438,243 - 8,489,129 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0168,282,606 - 8,333,507 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0168,351,023 - 8,402,007 (+)NCBIUU_Cfam_GSD_1.0
Slc37a3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511814,718,157 - 14,765,937 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049365924,453,811 - 4,489,343 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC37A3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl189,383,792 - 9,452,570 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1189,383,770 - 9,442,787 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21810,004,028 - 10,019,295 (-)NCBISscrofa10.2Sscrofa10.2susScr3
Sscrofa10.2189,890,416 - 9,892,652 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SLC37A3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.121109,101,841 - 109,179,864 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl21109,115,256 - 109,164,022 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660725,764,589 - 5,826,474 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Slc37a3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476520,534,721 - 20,588,599 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476520,537,294 - 20,588,609 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SLC37A3
35 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 copy number gain See cases [RCV000050876] Chr7:129310166..159282390 [GRCh38]
Chr7:128950007..159075079 [GRCh37]
Chr7:128737243..158767840 [NCBI36]
Chr7:7q32.1-36.3
pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 copy number gain See cases [RCV000051101] Chr7:132850196..159325876 [GRCh38]
Chr7:132534956..159118566 [GRCh37]
Chr7:132185496..158811327 [NCBI36]
Chr7:7q32.3-36.3
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 7q34(chr7:138795539-140364913)x3 copy number gain See cases [RCV000053550] Chr7:138795539..140364913 [GRCh38]
Chr7:138480284..140064713 [GRCh37]
Chr7:138130824..139711182 [NCBI36]
Chr7:7q34
uncertain significance
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 copy number gain See cases [RCV000053576] Chr7:136309982..159307523 [GRCh38]
Chr7:135994730..159100212 [GRCh37]
Chr7:135645270..158792973 [NCBI36]
Chr7:7q33-36.3
pathogenic
GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] Chr7:132023155..149309794 [GRCh38]
Chr7:131707914..149006885 [GRCh37]
Chr7:131358454..148637818 [NCBI36]
Chr7:7q32.3-36.1
pathogenic
GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1 copy number loss See cases [RCV000054173] Chr7:135414108..144140219 [GRCh38]
Chr7:135098857..143837312 [GRCh37]
Chr7:134749397..143468245 [NCBI36]
Chr7:7q33-35
pathogenic
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] Chr7:139365967..159282531 [GRCh38]
Chr7:139050713..159075220 [GRCh37]
Chr7:138701253..158767981 [NCBI36]
Chr7:7q34-36.3
pathogenic
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 7q33-36.2(chr7:137751200-154815582)x3 copy number gain See cases [RCV000136592] Chr7:137751200..154815582 [GRCh38]
Chr7:137435946..154607292 [GRCh37]
Chr7:137086486..154238225 [NCBI36]
Chr7:7q33-36.2
pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 copy number loss See cases [RCV000138120] Chr7:134666829..158591882 [GRCh38]
Chr7:134351581..158384574 [GRCh37]
Chr7:134002121..158077335 [NCBI36]
Chr7:7q33-36.3
pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3
pathogenic
GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1 copy number loss See cases [RCV000138903] Chr7:135017687..148807400 [GRCh38]
Chr7:134702438..148504492 [GRCh37]
Chr7:134352978..148135425 [NCBI36]
Chr7:7q33-36.1
pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 copy number gain See cases [RCV000139654] Chr7:132444095..159335866 [GRCh38]
Chr7:132128854..159128556 [GRCh37]
Chr7:131779394..158821317 [NCBI36]
Chr7:7q32.3-36.3
pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3
pathogenic
GRCh38/hg38 7q34(chr7:140337173-140406740)x3 copy number gain See cases [RCV000140935] Chr7:140337173..140406740 [GRCh38]
Chr7:140036973..140106540 [GRCh37]
Chr7:139683442..139753009 [NCBI36]
Chr7:7q34
likely benign
GRCh38/hg38 7q34(chr7:139476271-140449156)x1 copy number loss See cases [RCV000142350] Chr7:139476271..140449156 [GRCh38]
Chr7:139161017..140148956 [GRCh37]
Chr7:138811557..139795425 [NCBI36]
Chr7:7q34
uncertain significance
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 copy number gain See cases [RCV000142802] Chr7:131228764..159335866 [GRCh38]
Chr7:130913523..159128556 [GRCh37]
Chr7:130564063..158821317 [NCBI36]
Chr7:7q32.3-36.3
pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 copy number gain See cases [RCV000143754] Chr7:131171478..159327017 [GRCh38]
Chr7:130856237..159119707 [GRCh37]
Chr7:130506777..158812468 [NCBI36]
Chr7:7q32.3-36.3
pathogenic
GRCh38/hg38 7q34-35(chr7:140061285-144622893)x3 copy number gain See cases [RCV000143724] Chr7:140061285..144622893 [GRCh38]
Chr7:139761085..144319986 [GRCh37]
Chr7:139407554..143950919 [NCBI36]
Chr7:7q34-35
uncertain significance
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 copy number gain See cases [RCV000143707] Chr7:132438072..159327017 [GRCh38]
Chr7:132122831..159119707 [GRCh37]
Chr7:131773371..158812468 [NCBI36]
Chr7:7q32.3-36.3
pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) copy number gain not provided [RCV000767558] Chr7:128312450..159119220 [GRCh37]
Chr7:7q32.1-36.3
pathogenic
GRCh37/hg19 7q34(chr7:140070378-140129626)x3 copy number gain Premature ovarian failure [RCV000225296] Chr7:140070378..140129626 [GRCh37]
Chr7:7q34
uncertain significance
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 copy number gain See cases [RCV000449264] Chr7:137589621..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
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
GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 copy number loss See cases [RCV000448836] Chr7:133799185..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 copy number gain See cases [RCV000447956] Chr7:128276078..159119707 [GRCh37]
Chr7:7q32.1-36.3
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 7q33-36.3(chr7:136758593-159119707)x3 copy number gain See cases [RCV000510490] Chr7:136758593..159119707 [GRCh37]
Chr7:7q33-36.3
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 7q33-36.3(chr7:137917376-159119707)x1 copy number loss See cases [RCV000511889] Chr7:137917376..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
NM_207113.3(SLC37A3):c.215A>G (p.His72Arg) single nucleotide variant not specified [RCV004294638] Chr7:140369666 [GRCh38]
Chr7:140069466 [GRCh37]
Chr7:7q34
uncertain significance
GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3 copy number gain Neurodevelopmental disorder [RCV003327610] Chr7:138620939..159233475 [GRCh38]
Chr7:7q34-36.3
likely pathogenic
NM_207113.3(SLC37A3):c.1406T>C (p.Ile469Thr) single nucleotide variant not specified [RCV004301016] Chr7:140335491 [GRCh38]
Chr7:140035291 [GRCh37]
Chr7:7q34
uncertain significance
GRCh37/hg19 7q33-34(chr7:137434852-140349546)x3 copy number gain See cases [RCV000512176] Chr7:137434852..140349546 [GRCh37]
Chr7:7q33-34
uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
Single allele complex Renal transitional cell carcinoma [RCV000754611] Chr7:129367205..140482957 [GRCh37]
Chr7:7q32.2-34
likely 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 7q34-35(chr7:139623170-143710268)x3 copy number gain not provided [RCV000747069] Chr7:139623170..143710268 [GRCh37]
Chr7:7q34-35
benign
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 copy number gain not provided [RCV000747070] Chr7:139623170..158329903 [GRCh37]
Chr7:7q34-36.3
pathogenic
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
NM_207113.3(SLC37A3):c.1005C>T (p.Tyr335=) single nucleotide variant not provided [RCV000958997] Chr7:140348645 [GRCh38]
Chr7:140048445 [GRCh37]
Chr7:7q34
benign
NM_207113.3(SLC37A3):c.255C>A (p.Gly85=) single nucleotide variant not provided [RCV000960899] Chr7:140369626 [GRCh38]
Chr7:140069426 [GRCh37]
Chr7:7q34
benign
GRCh37/hg19 7q32.3-36.3(chr7:131414604-159126310)x1 copy number loss See cases [RCV001007432] Chr7:131414604..159126310 [GRCh37]
Chr7:7q32.3-36.3
pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3
pathogenic
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 copy number gain not provided [RCV000849569] Chr7:130592554..159119707 [GRCh37]
Chr7:7q32.3-36.3
pathogenic
NM_207113.3(SLC37A3):c.377T>C (p.Val126Ala) single nucleotide variant not specified [RCV004281590] Chr7:140358784 [GRCh38]
Chr7:140058584 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.882+9C>T single nucleotide variant not provided [RCV000960898] Chr7:140351264 [GRCh38]
Chr7:140051064 [GRCh37]
Chr7:7q34
benign
NM_207113.3(SLC37A3):c.839C>T (p.Ala280Val) single nucleotide variant not provided [RCV000956535] Chr7:140351316 [GRCh38]
Chr7:140051116 [GRCh37]
Chr7:7q34
benign
GRCh37/hg19 7q34(chr7:140055557-140128758)x1 copy number loss not provided [RCV001006021] Chr7:140055557..140128758 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.896A>T (p.Tyr299Phe) single nucleotide variant not specified [RCV004683719] Chr7:140348754 [GRCh38]
Chr7:140048554 [GRCh37]
Chr7:7q34
uncertain significance
GRCh37/hg19 7q33-35(chr7:133848099-145814115)x1 copy number loss Hypertelorism [RCV001801200] Chr7:133848099..145814115 [GRCh37]
Chr7:7q33-35
pathogenic
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q33-36.3(chr7:133851002-159119707)x3 copy number gain not provided [RCV001834520] Chr7:133851002..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
NC_000007.13:g.(?_137761265)_(141759786_?)dup duplication not provided [RCV002014827] Chr7:137761265..141759786 [GRCh37]
Chr7:7q33-34
uncertain significance
NC_000007.13:g.(?_138391369)_(141759786_?)del deletion RASopathy [RCV003113440]|not provided [RCV003109447] Chr7:138391369..141759786 [GRCh37]
Chr7:7q34
pathogenic|uncertain significance|no classifications from unflagged records
NC_000007.13:g.(?_130781014)_(150301047_?)del deletion not provided [RCV003116360] Chr7:130781014..150301047 [GRCh37]
Chr7:7q32.3-36.1
pathogenic
NM_207113.3(SLC37A3):c.329A>T (p.Asn110Ile) single nucleotide variant not specified [RCV004683718] Chr7:140364454 [GRCh38]
Chr7:140064254 [GRCh37]
Chr7:7q34
uncertain significance
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
GRCh37/hg19 7q32.3-36.1(chr7:131779213-149042734)x1 copy number loss not provided [RCV002472560] Chr7:131779213..149042734 [GRCh37]
Chr7:7q32.3-36.1
pathogenic
NM_207113.3(SLC37A3):c.403T>C (p.Trp135Arg) single nucleotide variant not specified [RCV004139971] Chr7:140358758 [GRCh38]
Chr7:140058558 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.94T>G (p.Ser32Ala) single nucleotide variant not specified [RCV004090169] Chr7:140380386 [GRCh38]
Chr7:140080186 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.940C>G (p.Pro314Ala) single nucleotide variant not specified [RCV004095832] Chr7:140348710 [GRCh38]
Chr7:140048510 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.232G>A (p.Glu78Lys) single nucleotide variant not specified [RCV004097554] Chr7:140369649 [GRCh38]
Chr7:140069449 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.164G>A (p.Ser55Asn) single nucleotide variant not specified [RCV004197034] Chr7:140380316 [GRCh38]
Chr7:140080116 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.601C>T (p.Leu201Phe) single nucleotide variant not specified [RCV004205797] Chr7:140355685 [GRCh38]
Chr7:140055485 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.1439T>C (p.Ile480Thr) single nucleotide variant not specified [RCV004089692] Chr7:140335458 [GRCh38]
Chr7:140035258 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.244C>G (p.Leu82Val) single nucleotide variant not specified [RCV004072651] Chr7:140369637 [GRCh38]
Chr7:140069437 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.152A>G (p.Gln51Arg) single nucleotide variant not specified [RCV004174839] Chr7:140380328 [GRCh38]
Chr7:140080128 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.1117G>C (p.Gly373Arg) single nucleotide variant not specified [RCV004142329] Chr7:140345878 [GRCh38]
Chr7:140045678 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.859T>C (p.Cys287Arg) single nucleotide variant not specified [RCV004221971] Chr7:140351296 [GRCh38]
Chr7:140051096 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.664G>A (p.Val222Ile) single nucleotide variant not specified [RCV004221071] Chr7:140352101 [GRCh38]
Chr7:140051901 [GRCh37]
Chr7:7q34
likely benign
NM_207113.3(SLC37A3):c.242C>T (p.Thr81Ile) single nucleotide variant not specified [RCV004306538] Chr7:140369639 [GRCh38]
Chr7:140069439 [GRCh37]
Chr7:7q34
uncertain significance
GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3 copy number gain Neurodevelopmental disorder [RCV003327609] Chr7:137463392..159345973 [GRCh38]
Chr7:7q33-36.3
pathogenic
NM_207113.3(SLC37A3):c.1450G>T (p.Val484Leu) single nucleotide variant not specified [RCV004350205] Chr7:140335447 [GRCh38]
Chr7:140035247 [GRCh37]
Chr7:7q34
uncertain significance
GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1 copy number loss not provided [RCV003482988] Chr7:135639005..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3 copy number gain not specified [RCV003986713] Chr7:137456457..159119707 [GRCh37]
Chr7:7q33-36.3
pathogenic
NM_207113.3(SLC37A3):c.253G>A (p.Gly85Ser) single nucleotide variant not specified [RCV004459416] Chr7:140369628 [GRCh38]
Chr7:140069428 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.392C>T (p.Ala131Val) single nucleotide variant not specified [RCV004459420] Chr7:140358769 [GRCh38]
Chr7:140058569 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.608A>G (p.Tyr203Cys) single nucleotide variant not specified [RCV004459421] Chr7:140355678 [GRCh38]
Chr7:140055478 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.1009G>A (p.Val337Ile) single nucleotide variant not specified [RCV004459415] Chr7:140348641 [GRCh38]
Chr7:140048441 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.376G>T (p.Val126Leu) single nucleotide variant not specified [RCV004459419] Chr7:140358785 [GRCh38]
Chr7:140058585 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.971A>G (p.Lys324Arg) single nucleotide variant not specified [RCV004459422] Chr7:140348679 [GRCh38]
Chr7:140048479 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.298T>G (p.Phe100Val) single nucleotide variant not specified [RCV004459417] Chr7:140364485 [GRCh38]
Chr7:140064285 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.320A>T (p.Asp107Val) single nucleotide variant not specified [RCV004459418] Chr7:140364463 [GRCh38]
Chr7:140064263 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.1419G>A (p.Ser473=) single nucleotide variant not specified [RCV004674647] Chr7:140335478 [GRCh38]
Chr7:140035278 [GRCh37]
Chr7:7q34
likely benign
NM_207113.3(SLC37A3):c.1235G>A (p.Arg412His) single nucleotide variant not specified [RCV004674648] Chr7:140343503 [GRCh38]
Chr7:140043303 [GRCh37]
Chr7:7q34
uncertain significance
NM_207113.3(SLC37A3):c.1307T>C (p.Ile436Thr) single nucleotide variant not specified [RCV004674646] Chr7:140343431 [GRCh38]
Chr7:140043231 [GRCh37]
Chr7:7q34
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:7285
Count of miRNA genes:1388
Interacting mature miRNAs:1832
Transcripts:ENST00000326232, ENST00000340308, ENST00000429996, ENST00000447932, ENST00000460560, ENST00000461089, ENST00000462881, ENST00000464834, ENST00000464865, ENST00000467233, ENST00000469193, ENST00000469636, ENST00000473060, ENST00000473707, ENST00000477006, ENST00000477571, ENST00000484416, ENST00000485139, ENST00000485538, ENST00000485734, ENST00000485861, ENST00000487319, ENST00000490760, ENST00000491357, ENST00000491505, ENST00000492027, ENST00000493423, ENST00000495257, ENST00000498469
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
597140114GWAS1236188_Heducational attainment QTL GWAS1236188 (human)4e-08educational attainment7140346237140346238Human
597077225GWAS1173299_Hnecrotizing enterocolitis QTL GWAS1173299 (human)0.000006necrotizing enterocolitis7140387149140387150Human

Markers in Region
SHGC-32230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377140,033,570 - 140,033,701UniSTSGRCh37
Build 367139,680,039 - 139,680,170RGDNCBI36
Celera7134,755,319 - 134,755,450RGD
Cytogenetic Map7q34UniSTS
HuRef7134,326,603 - 134,326,734UniSTS
CRA_TCAGchr7v27139,362,389 - 139,362,520UniSTS
TNG Radiation Hybrid Map762755.0UniSTS
GeneMap99-G3 RH Map76048.0UniSTS
SHGC-24030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377140,033,695 - 140,033,784UniSTSGRCh37
Build 367139,680,164 - 139,680,253RGDNCBI36
Celera7134,755,444 - 134,755,533RGD
Cytogenetic Map7q34UniSTS
HuRef7134,326,728 - 134,326,817UniSTS
CRA_TCAGchr7v27139,362,514 - 139,362,603UniSTS
RH80207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377140,033,568 - 140,033,773UniSTSGRCh37
Build 367139,680,037 - 139,680,242RGDNCBI36
Celera7134,755,317 - 134,755,522RGD
Cytogenetic Map7q34UniSTS
HuRef7134,326,601 - 134,326,806UniSTS
CRA_TCAGchr7v27139,362,387 - 139,362,592UniSTS
RH104127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377140,054,408 - 140,054,536UniSTSGRCh37
Build 367139,700,877 - 139,701,005RGDNCBI36
Celera7134,776,156 - 134,776,284RGD
Cytogenetic Map7q34UniSTS
HuRef7134,347,441 - 134,347,569UniSTS
CRA_TCAGchr7v27139,383,226 - 139,383,354UniSTS
GeneMap99-GB4 RH Map7641.27UniSTS
D1S3695  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p34-p12UniSTS
Cytogenetic Map6q27UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
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Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001287498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_207113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_156489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_156490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_156491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_156492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC093087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK131347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL691676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC046567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM669953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD101739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN261821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ834428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ834542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX752660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA064851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA582415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA750092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB481623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC376346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000326232   ⟹   ENSP00000321498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,333,752 - 140,398,530 (-)Ensembl
Ensembl Acc Id: ENST00000340308   ⟹   ENSP00000343358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,333,752 - 140,398,457 (-)Ensembl
Ensembl Acc Id: ENST00000447932   ⟹   ENSP00000397481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,333,752 - 140,398,502 (-)Ensembl
Ensembl Acc Id: ENST00000460560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,335,321 - 140,398,508 (-)Ensembl
Ensembl Acc Id: ENST00000461089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,358,640 - 140,398,550 (-)Ensembl
Ensembl Acc Id: ENST00000462881   ⟹   ENSP00000419410
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,364,459 - 140,398,478 (-)Ensembl
Ensembl Acc Id: ENST00000464834   ⟹   ENSP00000417449
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,351,889 - 140,369,662 (-)Ensembl
Ensembl Acc Id: ENST00000464865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,351,520 - 140,398,504 (-)Ensembl
Ensembl Acc Id: ENST00000467233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,379,878 - 140,382,474 (-)Ensembl
Ensembl Acc Id: ENST00000469193   ⟹   ENSP00000419024
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,352,062 - 140,398,532 (-)Ensembl
Ensembl Acc Id: ENST00000469636   ⟹   ENSP00000418610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,333,791 - 140,343,489 (-)Ensembl
Ensembl Acc Id: ENST00000473060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,333,754 - 140,344,086 (-)Ensembl
Ensembl Acc Id: ENST00000473707
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,351,876 - 140,369,682 (-)Ensembl
Ensembl Acc Id: ENST00000477006   ⟹   ENSP00000417461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,335,290 - 140,345,907 (-)Ensembl
Ensembl Acc Id: ENST00000477571   ⟹   ENSP00000417365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,293,693 - 140,398,489 (-)Ensembl
Ensembl Acc Id: ENST00000484416   ⟹   ENSP00000419701
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,351,361 - 140,364,491 (-)Ensembl
Ensembl Acc Id: ENST00000485139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,335,472 - 140,337,825 (-)Ensembl
Ensembl Acc Id: ENST00000485538   ⟹   ENSP00000417380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,334,989 - 140,343,530 (-)Ensembl
Ensembl Acc Id: ENST00000485734   ⟹   ENSP00000419285
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,335,455 - 140,352,100 (-)Ensembl
Ensembl Acc Id: ENST00000485861   ⟹   ENSP00000420771
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,348,626 - 140,369,654 (-)Ensembl
Ensembl Acc Id: ENST00000487319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,348,458 - 140,351,405 (-)Ensembl
Ensembl Acc Id: ENST00000490760   ⟹   ENSP00000418585
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,351,431 - 140,398,481 (-)Ensembl
Ensembl Acc Id: ENST00000491357   ⟹   ENSP00000418136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,334,891 - 140,348,686 (-)Ensembl
Ensembl Acc Id: ENST00000491505   ⟹   ENSP00000417181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,382,483 - 140,404,310 (-)Ensembl
Ensembl Acc Id: ENST00000492027   ⟹   ENSP00000417447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,335,105 - 140,351,357 (-)Ensembl
Ensembl Acc Id: ENST00000493423
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,400,336 - 140,404,433 (-)Ensembl
Ensembl Acc Id: ENST00000495257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,379,259 - 140,398,507 (-)Ensembl
Ensembl Acc Id: ENST00000498469   ⟹   ENSP00000418158
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7140,334,870 - 140,345,911 (-)Ensembl
RefSeq Acc Id: NM_001287498   ⟹   NP_001274427
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
HuRef7134,326,585 - 134,391,056 (-)NCBI
CHM1_17139,968,423 - 140,033,256 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363373   ⟹   NP_001350302
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363374   ⟹   NP_001350303
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363375   ⟹   NP_001350304
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363376   ⟹   NP_001350305
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363377   ⟹   NP_001350306
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363378   ⟹   NP_001350307
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NM_032295   ⟹   NP_115671
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
GRCh377140,033,552 - 140,104,024 (-)NCBI
Build 367139,680,021 - 139,744,780 (-)NCBI Archive
Celera7134,755,301 - 134,820,377 (-)RGD
HuRef7134,326,585 - 134,391,056 (-)NCBI
CHM1_17139,968,423 - 140,033,256 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
CRA_TCAGchr7v27139,362,371 - 139,427,142 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_207113   ⟹   NP_996996
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
GRCh377140,033,552 - 140,104,024 (-)NCBI
Build 367139,680,021 - 139,744,780 (-)NCBI Archive
Celera7134,755,301 - 134,820,377 (-)RGD
HuRef7134,326,585 - 134,391,056 (-)NCBI
CHM1_17139,968,423 - 140,033,256 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
CRA_TCAGchr7v27139,362,371 - 139,427,142 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NR_156489
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NR_156490
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NR_156491
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: NR_156492
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047420947   ⟹   XP_047276903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
RefSeq Acc Id: XM_047420948   ⟹   XP_047276904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
RefSeq Acc Id: XM_047420949   ⟹   XP_047276905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
RefSeq Acc Id: XM_047420950   ⟹   XP_047276906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387140,333,752 - 140,398,530 (-)NCBI
RefSeq Acc Id: XM_054359213   ⟹   XP_054215188
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
RefSeq Acc Id: XM_054359214   ⟹   XP_054215189
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
RefSeq Acc Id: XM_054359215   ⟹   XP_054215190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
RefSeq Acc Id: XM_054359216   ⟹   XP_054215191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07141,647,320 - 141,712,712 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001274427 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350302 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350303 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350304 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350305 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350306 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350307 (Get FASTA)   NCBI Sequence Viewer  
  NP_115671 (Get FASTA)   NCBI Sequence Viewer  
  NP_996996 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276903 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276904 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276905 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276906 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215188 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215189 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215190 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215191 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH28380 (Get FASTA)   NCBI Sequence Viewer  
  AAH46567 (Get FASTA)   NCBI Sequence Viewer  
  AAQ93361 (Get FASTA)   NCBI Sequence Viewer  
  BAC11231 (Get FASTA)   NCBI Sequence Viewer  
  BAG54349 (Get FASTA)   NCBI Sequence Viewer  
  BAG59167 (Get FASTA)   NCBI Sequence Viewer  
  BAG61295 (Get FASTA)   NCBI Sequence Viewer  
  BAG62026 (Get FASTA)   NCBI Sequence Viewer  
  CAB66518 (Get FASTA)   NCBI Sequence Viewer  
  CAH05429 (Get FASTA)   NCBI Sequence Viewer  
  CAH05486 (Get FASTA)   NCBI Sequence Viewer  
  EAL24030 (Get FASTA)   NCBI Sequence Viewer  
  EAL24031 (Get FASTA)   NCBI Sequence Viewer  
  EAW83943 (Get FASTA)   NCBI Sequence Viewer  
  EAW83944 (Get FASTA)   NCBI Sequence Viewer  
  EAW83945 (Get FASTA)   NCBI Sequence Viewer  
  EAW83946 (Get FASTA)   NCBI Sequence Viewer  
  EAW83947 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000321498
  ENSP00000321498.9
  ENSP00000343358
  ENSP00000343358.3
  ENSP00000397481
  ENSP00000397481.2
  ENSP00000417181.1
  ENSP00000417365.1
  ENSP00000417380.1
  ENSP00000417447.1
  ENSP00000417449.1
  ENSP00000417461.1
  ENSP00000418136.1
  ENSP00000418158.1
  ENSP00000418585.1
  ENSP00000418610.1
  ENSP00000419024.1
  ENSP00000419285.1
  ENSP00000419410.1
  ENSP00000419701.1
  ENSP00000420771.1
GenBank Protein Q8NCC5 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_115671   ⟸   NM_032295
- Peptide Label: isoform 2
- UniProtKB: Q8NCC5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_996996   ⟸   NM_207113
- Peptide Label: isoform 1
- UniProtKB: Q8NCC5 (UniProtKB/Swiss-Prot),   Q86SS4 (UniProtKB/Swiss-Prot),   Q6PIU7 (UniProtKB/Swiss-Prot),   Q9BQG7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001274427   ⟸   NM_001287498
- Peptide Label: isoform 3
- UniProtKB: Q8NCC5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001350304   ⟸   NM_001363375
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001350306   ⟸   NM_001363377
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001350305   ⟸   NM_001363376
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001350307   ⟸   NM_001363378
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001350303   ⟸   NM_001363374
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001350302   ⟸   NM_001363373
- Peptide Label: isoform 4
Ensembl Acc Id: ENSP00000419410   ⟸   ENST00000462881
Ensembl Acc Id: ENSP00000417461   ⟸   ENST00000477006
Ensembl Acc Id: ENSP00000417365   ⟸   ENST00000477571
Ensembl Acc Id: ENSP00000417449   ⟸   ENST00000464834
Ensembl Acc Id: ENSP00000418585   ⟸   ENST00000490760
Ensembl Acc Id: ENSP00000418136   ⟸   ENST00000491357
Ensembl Acc Id: ENSP00000417181   ⟸   ENST00000491505
Ensembl Acc Id: ENSP00000417447   ⟸   ENST00000492027
Ensembl Acc Id: ENSP00000418610   ⟸   ENST00000469636
Ensembl Acc Id: ENSP00000419024   ⟸   ENST00000469193
Ensembl Acc Id: ENSP00000321498   ⟸   ENST00000326232
Ensembl Acc Id: ENSP00000418158   ⟸   ENST00000498469
Ensembl Acc Id: ENSP00000419701   ⟸   ENST00000484416
Ensembl Acc Id: ENSP00000417380   ⟸   ENST00000485538
Ensembl Acc Id: ENSP00000419285   ⟸   ENST00000485734
Ensembl Acc Id: ENSP00000420771   ⟸   ENST00000485861
Ensembl Acc Id: ENSP00000397481   ⟸   ENST00000447932
Ensembl Acc Id: ENSP00000343358   ⟸   ENST00000340308
RefSeq Acc Id: XP_047276906   ⟸   XM_047420950
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047276905   ⟸   XM_047420949
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047276903   ⟸   XM_047420947
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276904   ⟸   XM_047420948
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054215191   ⟸   XM_054359216
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054215190   ⟸   XM_054359215
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054215188   ⟸   XM_054359213
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054215189   ⟸   XM_054359214
- Peptide Label: isoform X2
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NCC5-F1-model_v2 AlphaFold Q8NCC5 1-494 view protein structure

Promoters
RGD ID:6806193
Promoter ID:HG_KWN:59953
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_032295,   NM_207113,   UC010LNH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367139,744,464 - 139,744,964 (-)MPROMDB
RGD ID:7212097
Promoter ID:EPDNEW_H11795
Type:initiation region
Name:SLC37A3_1
Description:solute carrier family 37 member 3
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
GRCh387140,398,514 - 140,398,574EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20651 AgrOrtholog
COSMIC SLC37A3 COSMIC
Ensembl Genes ENSG00000157800 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000326232 ENTREZGENE
  ENST00000326232.14 UniProtKB/Swiss-Prot
  ENST00000340308 ENTREZGENE
  ENST00000340308.7 UniProtKB/Swiss-Prot
  ENST00000447932 ENTREZGENE
  ENST00000447932.6 UniProtKB/Swiss-Prot
  ENST00000462881.1 UniProtKB/TrEMBL
  ENST00000464834.5 UniProtKB/TrEMBL
  ENST00000469193.5 UniProtKB/TrEMBL
  ENST00000469636.1 UniProtKB/TrEMBL
  ENST00000477006.1 UniProtKB/TrEMBL
  ENST00000477571.5 UniProtKB/TrEMBL
  ENST00000484416.5 UniProtKB/TrEMBL
  ENST00000485538.1 UniProtKB/TrEMBL
  ENST00000485734.1 UniProtKB/TrEMBL
  ENST00000485861.5 UniProtKB/TrEMBL
  ENST00000490760.5 UniProtKB/TrEMBL
  ENST00000491357.5 UniProtKB/TrEMBL
  ENST00000491505.1 UniProtKB/TrEMBL
  ENST00000492027.5 UniProtKB/TrEMBL
  ENST00000498469.5 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1250.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000157800 GTEx
HGNC ID HGNC:20651 ENTREZGENE
Human Proteome Map SLC37A3 Human Proteome Map
InterPro MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sugar_P_transporter UniProtKB/Swiss-Prot
KEGG Report hsa:84255 UniProtKB/Swiss-Prot
NCBI Gene 84255 ENTREZGENE
OMIM 619137 OMIM
PANTHER MAJOR FACILITATOR SUPERFAMILY TRANSPORTER 16, ISOFORM B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUGAR PHOSPHATE EXCHANGER 3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MFS_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134895240 PharmGKB
PIRSF Hexose_phosphate_transp UniProtKB/Swiss-Prot
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt C9J4S7_HUMAN UniProtKB/TrEMBL
  C9JZ37_HUMAN UniProtKB/TrEMBL
  F8WAR9_HUMAN UniProtKB/TrEMBL
  F8WC97_HUMAN UniProtKB/TrEMBL
  F8WF28_HUMAN UniProtKB/TrEMBL
  H7C4I4_HUMAN UniProtKB/TrEMBL
  H7C4J2_HUMAN UniProtKB/TrEMBL
  H7C4J3_HUMAN UniProtKB/TrEMBL
  H7C4J5_HUMAN UniProtKB/TrEMBL
  H7C4U0_HUMAN UniProtKB/TrEMBL
  H7C4U5_HUMAN UniProtKB/TrEMBL
  H7C4Z5_HUMAN UniProtKB/TrEMBL
  H7C594_HUMAN UniProtKB/TrEMBL
  H7C5E7_HUMAN UniProtKB/TrEMBL
  H7C5T4_HUMAN UniProtKB/TrEMBL
  Q6PIU7 ENTREZGENE
  Q86SS4 ENTREZGENE
  Q8NCC5 ENTREZGENE
  Q9BQG7 ENTREZGENE
  SPX3_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q6PIU7 UniProtKB/Swiss-Prot
  Q86SS4 UniProtKB/Swiss-Prot
  Q9BQG7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-05 SLC37A3  solute carrier family 37 member 3    solute carrier family 37, member 3  Symbol and/or name change 5135510 APPROVED
2013-07-23 SLC37A3  solute carrier family 37, member 3    solute carrier family 37 (glycerol-3-phosphate transporter), member 3  Symbol and/or name change 5135510 APPROVED