solute carrier family 17 member 5

Preferred Label : solute carrier family 17 member 5;

Approved symbol HGNC : SLC17A5;

Name synonyms HGNC : acidic sugar transporter; Salla disease; infantile sialic acid storage disorder;

Alias symbols HGNC : SD; AST; SIALIN; ISSD; SLD; NSD;

Chromosome HGNC : 6q13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000119899;

Details

Origin ID

HGNC:10933;

UMLS CUI

C1420113;

Automatic exact mappings (from CISMeF team)
- Infantile sialic acid storage disease [OMIM Phenotype]
- Salla disease [OMIM Phenotype]
- Salla disease [ORDO Disease]
- Sialic Acid Storage Disease [NCIt concept]
- Solute carrier family 17 (acidic sugar transporter), member 5 [OMIM gene]
NCIt concept
- SLC17A5 Gene [NCIt concept]
OMIM gene
- Solute carrier family 17 (acidic sugar transporter), member 5 [OMIM gene]
Orphanet gene
- solute carrier family 17 member 5 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC17A5 gene [LOINC component]
- Solute carrier family 17 (acidic sugar transporter), member 5 [OMIM gene]

Keyword's position in hierarchy(ies) :

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