Solute carrier family 38 (amino acid transporter), member 3

Preferred Label : Solute carrier family 38 (amino acid transporter), member 3;

Symbol : SLC38A3;

CISMeF acronym : SLC38A3;

Type : Gene;

Alternative titles and symbols : Transport system n, protein 1; N-system amino acid transporter 1; SN1; G17; NAT1; SNAT3;

Ensembl ID : ENSG00000188338;

Prefixed ID : *604437;

Details

Origin ID

604437;

UMLS CUI

C1442750;

Automatic exact mappings (from CISMeF team)
- Arylamine N-Acetyltransferase 1 [NCIt concept]
- NAT1 Gene [NCIt concept]
- NAT1 wt Allele [NCIt concept]
- SLC38A3 Gene [NCIt concept]
- SLC38A3 wt Allele [NCIt concept]
- SLC6A2 wt Allele [NCIt concept]
- Sodium-Coupled Neutral Amino Acid Transporter 3 [NCIt concept]
- solute carrier family 38 member 3 [HGNC gene]
HGNC gene
- solute carrier family 38 member 3 [HGNC gene]
NCIt concept(s)
- SLC38A3 Gene [NCIt concept]
- SLC38A3 wt Allele [NCIt concept]
- Sodium-Coupled Neutral Amino Acid Transporter 3 [NCIt concept]
ORDO concept(s)
- solute carrier family 38 member 3 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 102 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC38A3 Gene [NCIt concept]
- solute carrier family 38 member 3 [HGNC gene]

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