solute carrier family 6 member 19

Preferred Label : solute carrier family 6 member 19;

Approved symbol HGNC : SLC6A19;

Name synonyms HGNC : broad neutral amino acid transporter 1; Hartnup disease; Sodium-dependent neutral amino acid transporter B(0)AT1;

Alias symbols HGNC : B0AT1;

Chromosome HGNC : 5p15.33;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000174358;

Details

Origin ID

HGNC:27960;

UMLS CUI

C1428660;

Automatic exact mappings (from CISMeF team)
- Hartnup Disease [NCIt concept]
- Hartnup disease [DO Concept]
- Hartnup disease [PASCAL descriptor]
- Hartnup disease [MedDRA Preferred Term]
- Hartnup disease [ORDO Disease]
- Hartnup disorder [OMIM Phenotype]
- Hartnup syndrome [ICD-11 More detail]
- Neutral 1 amino acid transport defect (disorder) [SNOMED CT concept]
- Sodium-Dependent Neutral Amino Acid Transporter B(0)AT1 [NCIt concept]
- Solute carrier family 6 (neurotransmitter transporter), member 19 [OMIM gene]
- hartnup disease [MeSH concept]
- hartnup disease [MeSH Descriptor]
- solute carrier family 6 member 19 [ORDO Gene]
NCIt concept
- SLC6A19 Gene [NCIt concept]
OMIM gene
- Solute carrier family 6 (neurotransmitter transporter), member 19 [OMIM gene]
Orphanet gene
- solute carrier family 6 member 19 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC6A19 Gene [NCIt concept]
- Solute carrier family 6 (neurotransmitter transporter), member 19 [OMIM gene]

Keyword's position in hierarchy(ies) :

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