ARHGAP31 wt Allele

Preferred Label : ARHGAP31 wt Allele;

NCIt synonyms : AOS1; CDGAP; Rho GTPase Activating Protein 31 wt Allele; KIAA1204;

NCIt definition : Human ARHGAP31 wild-type allele is located within 3q13.32-q13.33 and is approximately 126 kb in length. This allele, which encodes Rho GTPase-activating protein 31, is involved in the regulation of GTPase activities of RAC1 and CDC42. Mutation of the gene is associated with Adams-Oliver syndrome 1.;

NCI Metathesaurus CUI : CL1778346;

GenBank Accession Number : NM_020754;

Details

Origin ID

C185732;

UMLS CUI

C5575275;

Automatic exact mappings (from CISMeF team)
- Adams-oliver syndrome 1 [OMIM Phenotype]
- Rho GTPase activating protein 31 [ORDO Gene]
- Rho gtpase-activating protein 31 [OMIM gene]
- Sumo1-activating enzyme, subunit 1 [OMIM gene]
OMIM relation
- Rho gtpase-activating protein 31 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

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