WIPF1 wt Allele

Preferred Label : WIPF1 wt Allele;

NCIt synonyms : WASPIP; WAS/WASL-Interacting Protein Family, Member 1 Gene; WIP; WAS/WASL Interacting Protein Family Member 1 wt Allele; PRPL-2; WAS2; WAS/WASL Interacting Protein Family, Member 1 Gene;

NCIt definition : Human WIPF1 wild-type allele is located in the vicinity of 2q31.1 and is approximately 123 kb in length. This allele, which encodes WAS/WASL-interacting protein family member 1 protein, plays a role in both cytoskeletal remodeling and stabilization of Wiskott-Aldrich syndrome protein. Mutation of the gene is associated with Wiskott-Aldrich syndrome 2.;

NCI Metathesaurus CUI : CL1642667;

GenBank Accession Number : AF031588;

Details

Origin ID

C176615;

UMLS CUI

C5444608;

Automatic exact mappings (from CISMeF team)
- WAS/WASL interacting protein family member 1 [ORDO Gene]
- Was/wasl-interacting protein family, member 1 [OMIM gene]
- Wiskott-aldrich syndrome 2 [OMIM Phenotype]
OMIM relation
- Was/wasl-interacting protein family, member 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2q31.1 [NCIt concept]
gene_is_element_in_pathway
- Endocytosis Pathway [NCIt concept]
- Pathogenic Escherichia coli Infection Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Modeling [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

Keyword's position in hierarchy(ies) :

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