WDR26 wt Allele

Preferred Label : WDR26 wt Allele;

NCIt synonyms : WD Repeat Domain 26 wt Allele; FLJ21016; PRO0852; Glucose-Induced Degradation-Deficient Protein 7, S. cerevisiae, Homolog of Gene; GID7; CDW2; MIP2; GID Complex, Subunit 7 Gene; GID Complex Subunit 7 Homolog (S. cerevisiae) Gene; SKDEAS;

NCIt definition : Human WDR26 wild-type allele is located within 1q42.11-q42.12 and is approximately 52 kb in length. This allele, which encodes WD repeat-containing protein 26, plays a role in the regulation of G protein activity. Mutation of the gene is associated with Skraban-Deardorff syndrome.;

NCI Metathesaurus CUI : CL541506;

GenBank Accession Number : AK024669;

Details

Origin ID

C143017;

UMLS CUI

C4552609;

Automatic exact mappings (from CISMeF team)
- Chemokine, cxc motif, ligand 2 [OMIM gene]
- WD repeat domain 26 [ORDO Gene]
- Wd repeat-containing protein 26 [OMIM gene]
OMIM relation
- Wd repeat-containing protein 26 [OMIM gene]
See also inter- (CISMeF)
- Skraban-deardorff syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- G Protein-Coupled Receptor Signaling [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Receptor Signaling [NCIt concept]
- Signal Transduction [NCIt concept]
- Subcellular Protein Targeting [NCIt concept]

Keyword's position in hierarchy(ies) :

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