SLC38A3 (solute carrier family 38 member 3) - Rat Genome Database

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Gene: SLC38A3 (solute carrier family 38 member 3) Homo sapiens
Analyze
Symbol: SLC38A3
Name: solute carrier family 38 member 3
RGD ID: 730997
HGNC Page HGNC
Description: Enables L-amino acid transmembrane transporter activity. Involved in amino acid transport. Located in plasma membrane; PARTICIPATES IN glutamate signaling pathway; INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; 2-hydroxypropanoic acid.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: G17; N-system amino acid transporter 1; Na(+)-coupled neutral amino acid transporter 3; NAT1; SN1; SNAT3; sodium-coupled neutral amino acid transporter 3; solute carrier family 38, member 3; system N amino acid transporter 1; system N1 Na+ and H+-coupled glutamine transporter
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl350,205,246 - 50,221,486 (+)EnsemblGRCh38hg38GRCh38
GRCh38350,205,268 - 50,221,486 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37350,242,704 - 50,258,918 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36350,217,696 - 50,233,410 (+)NCBINCBI36hg18NCBI36
Build 34350,217,708 - 50,233,406NCBI
Celera350,215,521 - 50,231,235 (+)NCBI
Cytogenetic Map3p21.31NCBI
HuRef350,298,378 - 50,314,094 (+)NCBIHuRef
CHM1_1350,194,967 - 50,210,681 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,1-dichloroethene  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-hydroxypropanoic acid  (EXP)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-chloropropane-1,2-diol  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acetylleucyl-leucyl-norleucinal  (ISO)
acrylamide  (EXP,ISO)
aflatoxin B1  (EXP,ISO)
aflatoxin B2  (EXP)
ammonium chloride  (ISO)
benzo[a]pyrene  (EXP)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
Brodifacoum  (ISO)
cadmium dichloride  (EXP)
carbamazepine  (EXP)
clofibric acid  (ISO)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
doxorubicin  (EXP)
endosulfan  (EXP)
ethanol  (ISO)
furan  (ISO)
glafenine  (ISO)
hydrogen chloride  (ISO)
ketamine  (ISO)
lactacystin  (ISO)
manganese atom  (ISO)
manganese(0)  (ISO)
manganese(II) chloride  (ISO)
N-nitrosodiethylamine  (ISO)
nickel sulfate  (EXP)
nitrofen  (ISO)
O-methyleugenol  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
phorbol 13-acetate 12-myristate  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
propiconazole  (ISO)
quercetin  (EXP)
rac-lactic acid  (EXP)
sodium arsenite  (EXP)
sulforaphane  (EXP)
sunitinib  (EXP)
tauroursodeoxycholic acid  (ISO)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
triptonide  (ISO)
troglitazone  (EXP)
valproic acid  (EXP)
vancomycin  (ISO)
vinclozolin  (ISO)
zidovudine  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Short stature  (IAGP)
References

Additional References at PubMed
PMID:8889548   PMID:10823827   PMID:11076863   PMID:11085536   PMID:11230166   PMID:11256614   PMID:12477932   PMID:12788082   PMID:15094455   PMID:15342556   PMID:15489334   PMID:15489336  
PMID:16169070   PMID:16381901   PMID:16432833   PMID:16641997   PMID:18195088   PMID:19892400   PMID:20737472   PMID:21873635   PMID:21988832   PMID:23506890   PMID:24854847   PMID:26590417  
PMID:28202352   PMID:28514442   PMID:30280653  


Genomics

Comparative Map Data
SLC38A3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl350,205,246 - 50,221,486 (+)EnsemblGRCh38hg38GRCh38
GRCh38350,205,268 - 50,221,486 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37350,242,704 - 50,258,918 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36350,217,696 - 50,233,410 (+)NCBINCBI36hg18NCBI36
Build 34350,217,708 - 50,233,406NCBI
Celera350,215,521 - 50,231,235 (+)NCBI
Cytogenetic Map3p21.31NCBI
HuRef350,298,378 - 50,314,094 (+)NCBIHuRef
CHM1_1350,194,967 - 50,210,681 (+)NCBICHM1_1
Slc38a3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm399107,528,353 - 107,546,167 (-)NCBIGRCm39mm39
GRCm39 Ensembl9107,527,833 - 107,546,729 (-)Ensembl
GRCm389107,651,154 - 107,668,968 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl9107,650,634 - 107,669,530 (-)EnsemblGRCm38mm10GRCm38
MGSCv379107,553,486 - 107,569,705 (-)NCBIGRCm37mm9NCBIm37
MGSCv369107,509,256 - 107,525,475 (-)NCBImm8
Celera9107,256,617 - 107,273,287 (-)NCBICelera
Cytogenetic Map9F1NCBI
cM Map958.69NCBI
Slc38a3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.28108,323,889 - 108,339,959 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl8108,323,894 - 108,339,988 (-)Ensembl
Rnor_6.08116,406,258 - 116,423,752 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl8116,406,241 - 116,422,366 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.08115,761,368 - 115,779,081 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.48112,898,405 - 112,914,444 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.18112,917,859 - 112,933,899 (-)NCBI
Celera8107,630,163 - 107,646,202 (-)NCBICelera
Cytogenetic Map8q32NCBI
Slc38a3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555322,023,694 - 2,050,708 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555322,023,694 - 2,046,556 (+)NCBIChiLan1.0ChiLan1.0
SLC38A3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1351,367,939 - 51,383,657 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl351,367,939 - 51,383,657 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0350,133,631 - 50,149,394 (+)NCBIMhudiblu_PPA_v0panPan3
SLC38A3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12039,108,387 - 39,122,526 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2039,109,211 - 39,114,849 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2039,029,425 - 39,043,601 (-)NCBI
ROS_Cfam_1.02039,464,652 - 39,478,831 (-)NCBI
UMICH_Zoey_3.12038,832,227 - 38,846,403 (-)NCBI
UNSW_CanFamBas_1.02039,236,334 - 39,250,516 (-)NCBI
UU_Cfam_GSD_1.02039,515,831 - 39,530,233 (-)NCBI
Slc38a3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560264,989,382 - 65,005,427 (+)NCBI
SpeTri2.0NW_0049365291,749,919 - 1,765,885 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC38A3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1332,683,191 - 32,704,535 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11332,683,131 - 32,699,803 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21335,861,884 - 35,878,403 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SLC38A3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12211,591,680 - 11,606,291 (+)NCBI
ChlSab1.1 Ensembl2211,591,717 - 11,606,355 (+)Ensembl
Vero_WHO_p1.0NW_023666041155,378,802 - 155,395,004 (-)NCBI
Slc38a3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247304,078,084 - 4,092,330 (+)NCBI

Position Markers
RH75882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,257,630 - 50,257,865UniSTSGRCh37
Build 36350,232,634 - 50,232,869RGDNCBI36
Celera350,230,459 - 50,230,694RGD
Cytogenetic Map3p21.3UniSTS
HuRef350,313,317 - 50,313,552UniSTS
D3S3181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,244,124 - 50,244,283UniSTSGRCh37
Build 36350,219,128 - 50,219,287RGDNCBI36
Celera350,216,952 - 50,217,111RGD
Cytogenetic Map3p21.3UniSTS
HuRef350,299,809 - 50,299,968UniSTS
RH65839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,258,037 - 50,258,199UniSTSGRCh37
Build 36350,233,041 - 50,233,203RGDNCBI36
Celera350,230,866 - 50,231,028RGD
Cytogenetic Map3p21.3UniSTS
HuRef350,313,724 - 50,313,886UniSTS
GeneMap99-GB4 RH Map3162.74UniSTS
PMC22669P16  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,254,093 - 50,254,453UniSTSGRCh37
Build 36350,229,097 - 50,229,457RGDNCBI36
Celera350,226,922 - 50,227,282RGD
Cytogenetic Map3p21.3UniSTS
HuRef350,309,780 - 50,310,140UniSTS
SLC38A3_7985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,257,755 - 50,258,584UniSTSGRCh37
Build 36350,232,759 - 50,233,588RGDNCBI36
Celera350,230,584 - 50,231,413RGD
HuRef350,313,442 - 50,314,272UniSTS
STS-T62038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37350,258,117 - 50,258,365UniSTSGRCh37
Build 36350,233,121 - 50,233,369RGDNCBI36
Celera350,230,946 - 50,231,194RGD
Cytogenetic Map3p21.3UniSTS
HuRef350,313,804 - 50,314,052UniSTS
GeneMap99-GB4 RH Map3159.8UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3188
Count of miRNA genes:819
Interacting mature miRNAs:993
Transcripts:ENST00000414604, ENST00000417121, ENST00000417851, ENST00000420502, ENST00000427428, ENST00000439524, ENST00000445096, ENST00000445325, ENST00000456338, ENST00000541861
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High 1 1 1
Medium 9 4 511 427 3 425 360 335 1962 21 108 31 4 2 341
Low 761 1546 922 181 147 24 2080 1053 1731 199 1028 855 160 1 294 1631 3
Below cutoff 1589 1273 263 12 1003 12 1871 792 32 115 291 643 7 896 815 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000417121
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,217,917 - 50,218,680 (+)Ensembl
RefSeq Acc Id: ENST00000417851
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,217,736 - 50,218,668 (+)Ensembl
RefSeq Acc Id: ENST00000439524
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,215,267 - 50,217,293 (+)Ensembl
RefSeq Acc Id: ENST00000445096   ⟹   ENSP00000480466
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,205,286 - 50,218,672 (+)Ensembl
RefSeq Acc Id: ENST00000610458   ⟹   ENSP00000479737
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,205,246 - 50,214,757 (+)Ensembl
RefSeq Acc Id: ENST00000614032   ⟹   ENSP00000481301
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,205,271 - 50,221,486 (+)Ensembl
RefSeq Acc Id: ENST00000620404
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,205,279 - 50,214,914 (+)Ensembl
RefSeq Acc Id: ENST00000621456   ⟹   ENSP00000484379
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,207,683 - 50,214,768 (+)Ensembl
RefSeq Acc Id: ENST00000621714   ⟹   ENSP00000483959
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl350,205,268 - 50,217,995 (+)Ensembl
RefSeq Acc Id: NM_006841   ⟹   NP_006832
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38350,205,271 - 50,221,486 (+)NCBI
GRCh37350,242,692 - 50,258,406 (+)RGD
Build 36350,217,696 - 50,233,410 (+)NCBI Archive
Celera350,215,521 - 50,231,235 (+)RGD
HuRef350,298,378 - 50,314,094 (+)ENTREZGENE
CHM1_1350,194,954 - 50,210,686 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006712954   ⟹   XP_006713017
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38350,207,341 - 50,221,486 (+)NCBI
Sequence:
RefSeq Acc Id: XR_001739987
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38350,205,268 - 50,220,977 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_006832   ⟸   NM_006841
- UniProtKB: Q99624 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006713017   ⟸   XM_006712954
- Peptide Label: isoform X1
- UniProtKB: Q99624 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000483959   ⟸   ENST00000621714
RefSeq Acc Id: ENSP00000484379   ⟸   ENST00000621456
RefSeq Acc Id: ENSP00000479737   ⟸   ENST00000610458
RefSeq Acc Id: ENSP00000481301   ⟸   ENST00000614032
RefSeq Acc Id: ENSP00000480466   ⟸   ENST00000445096
Protein Domains
Aa_trans

Promoters
RGD ID:6864478
Promoter ID:EPDNEW_H5403
Type:multiple initiation site
Name:SLC38A3_1
Description:solute carrier family 38 member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38350,205,273 - 50,205,333EPDNEW
RGD ID:6801696
Promoter ID:HG_KWN:45105
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour
Transcripts:ENST00000341160,   NM_006841,   OTTHUMT00000345635,   OTTHUMT00000346672,   OTTHUMT00000346676,   OTTHUMT00000346677,   OTTHUMT00000346678,   UC003CYN.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36350,217,441 - 50,217,941 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p21.31-14.3(chr3:49461000-55314500)x1 copy number loss See cases [RCV000051511] Chr3:49461000..55314500 [GRCh38]
Chr3:49498433..55348528 [GRCh37]
Chr3:49473437..55323568 [NCBI36]
Chr3:3p21.31-14.3
pathogenic
GRCh38/hg38 3p21.31-21.2(chr3:45879883-50749922)x4 copy number gain See cases [RCV000133650] Chr3:45879883..50749922 [GRCh38]
Chr3:45921375..50787353 [GRCh37]
Chr3:45896379..50762357 [NCBI36]
Chr3:3p21.31-21.2
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
NM_006841.6(SLC38A3):c.1108C>A (p.Arg370Ser) single nucleotide variant Short stature [RCV000736229] Chr3:50218664 [GRCh38]
Chr3:50256096 [GRCh37]
Chr3:3p21.31
uncertain significance
NM_006841.6(SLC38A3):c.686T>C (p.Ile229Thr) single nucleotide variant Short stature [RCV000736230] Chr3:50217469 [GRCh38]
Chr3:50254901 [GRCh37]
Chr3:3p21.31
uncertain significance
NM_006841.6(SLC38A3):c.1441C>A (p.Leu481Met) single nucleotide variant Short stature [RCV000736231] Chr3:50220103 [GRCh38]
Chr3:50257535 [GRCh37]
Chr3:3p21.31
uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p21.31-21.1(chr3:45153770-53878616) copy number gain not provided [RCV000767704] Chr3:45153770..53878616 [GRCh37]
Chr3:3p21.31-21.1
pathogenic
GRCh37/hg19 3p21.31-21.2(chr3:48807193-51363558)x1 copy number loss not provided [RCV001259686] Chr3:48807193..51363558 [GRCh37]
Chr3:3p21.31-21.2
pathogenic
NC_000003.11:g.(?_50154507)_(50295122_?)dup duplication not provided [RCV001365176] Chr3:50154507..50295122 [GRCh37]
Chr3:3p21.31
uncertain significance
NC_000003.11:g.(?_48507870)_(50340407_?)del deletion Aicardi Goutieres syndrome 1 [RCV001380369] Chr3:48507870..50340407 [GRCh37]
Chr3:3p21.31
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18044 AgrOrtholog
COSMIC SLC38A3 COSMIC
Ensembl Genes ENSG00000188338 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000479737 UniProtKB/TrEMBL
  ENSP00000480466 UniProtKB/TrEMBL
  ENSP00000481301 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000483959 UniProtKB/TrEMBL
  ENSP00000484379 UniProtKB/TrEMBL
Ensembl Transcript ENST00000445096 UniProtKB/TrEMBL
  ENST00000610458 UniProtKB/TrEMBL
  ENST00000614032 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000621456 UniProtKB/TrEMBL
  ENST00000621714 UniProtKB/TrEMBL
GTEx ENSG00000188338 GTEx
HGNC ID HGNC:18044 ENTREZGENE
Human Proteome Map SLC38A3 Human Proteome Map
InterPro AA_transpt_TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10991 UniProtKB/Swiss-Prot
NCBI Gene 10991 ENTREZGENE
OMIM 604437 OMIM
Pfam Aa_trans UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38281 PharmGKB
UniProt A0A087WVW8_HUMAN UniProtKB/TrEMBL
  A0A087WWS5_HUMAN UniProtKB/TrEMBL
  A0A087X175_HUMAN UniProtKB/TrEMBL
  A0A087X1Q4_HUMAN UniProtKB/TrEMBL
  Q99624 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B2R8Q0 UniProtKB/Swiss-Prot
  Q6IB34 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 SLC38A3  solute carrier family 38 member 3    solute carrier family 38, member 3  Symbol and/or name change 5135510 APPROVED