CISD2 wt Allele

Preferred Label : CISD2 wt Allele;

NCIt synonyms : WFS2; Miner1; NAF-1; ZCD2; ERIS; MitoNEET Related 1 Gene; Wolfram Syndrome 2 Gene; Zinc Finger, CDGSH-Type Domain 2 Gene; CDGSH Iron Sulfur Domain 2 wt Allele;

NCIt definition : Human CISD2 wild-type allele is located in the vicinity of 4q24 and is approximately 24 kb in length. This allele, which encodes CDGSH iron-sulfur domain-containing protein 2, is involved in both iron-sulfur binding and autophagy. Mutation of the gene is associated with Wolfram syndrome 2.;

GenBank Accession Number : BX537971;

Details

Origin ID

C116300;

UMLS CUI

C3889433;

Automatic exact mappings (from CISMeF team)
- CDGSH iron sulfur domain 2 [ORDO Gene]
- Cdgsh iron sulfur domain protein 2 [OMIM gene]
- Nuclear assembly factor 1 ribonucleoprotein [OMIM gene]
- Stimulator of interferon response cgamp interactor 1 [OMIM gene]
- TNFAIP3 interacting protein 1 [ORDO Gene]
- Tnfaip3-interacting protein 1 [OMIM gene]
- Wolfram syndrome 2 [OMIM Phenotype]
- Wolfram syndrome 2 [DO Concept]
- stimulator of interferon response cGAMP interactor 1 [ORDO Gene]
OMIM relation
- Cdgsh iron sulfur domain protein 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Autophagy [NCIt concept]
- Ligand Binding [NCIt concept]
- Metal Ion Binding [NCIt concept]

Keyword's position in hierarchy(ies) :

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