Solute carrier family 26, member 5

Preferred Label : Solute carrier family 26, member 5;

Symbol : SLC26A5;

CISMeF acronym : SLC26A5;

Type : Gene;

Alternative titles and symbols : Prestin; PRES;

Included titles and symbols : Slc26a5a; Slc26a5b; Slc26a5c; Slc26a5d;

Ensembl ID : ENSG00000170615;

Prefixed ID : *604943;

Details

Origin ID

604943;

UMLS CUI

C1822756;

Automatic exact mappings (from CISMeF team)
- Pressure [LOINC component]
- Reversible Posterior Leukoencephalopathy Syndrome [NCIt concept]
- SLC26A5 gene [LOINC component]
- solute carrier family 26 member 5 [HGNC gene]
- solute carrier family 26 member 5 [ORDO Gene]
HGNC gene
- solute carrier family 26 member 5 [HGNC gene]
ORDO concept(s)
- solute carrier family 26 member 5 [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 61 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC26A5 gene [LOINC component]
- solute carrier family 26 member 5 [HGNC gene]

Keyword's position in hierarchy(ies) :

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