Wolframin er transmembrane glycoprotein

Preferred Label : Wolframin er transmembrane glycoprotein;

Symbol : WFS1;

CISMeF acronym : WFS1;

Type : Gene;

Alternative titles and symbols : WOLFRAMIN;

Ensembl ID : ENSG00000109501;

Prefixed ID : *606201;

Details

Origin ID

606201;

UMLS CUI

C1421501;

Automatic exact mappings (from CISMeF team)
- WFS1 gene [LOINC component]
- Wolfram syndrome 1 [DO Concept]
- wolframin ER transmembrane glycoprotein [ORDO Gene]
- wolframin ER transmembrane glycoprotein [HGNC gene]
HGNC gene
- wolframin ER transmembrane glycoprotein [HGNC gene]
ORDO concept(s)
- wolframin ER transmembrane glycoprotein [ORDO Gene]
Phenotypes related
- Cataract 41 [OMIM Phenotype]
- Deafness, autosomal dominant 6 [OMIM Phenotype]
- Type 2 diabetes mellitus [OMIM Phenotype]
- Wolfram syndrome 1 [OMIM Phenotype]
- Wolfram-like syndrome, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WFS1 gene [LOINC component]
- wolframin ER transmembrane glycoprotein [HGNC gene]

Keyword's position in hierarchy(ies) :

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