PLXNC1 wt Allele

Preferred Label : PLXNC1 wt Allele;

NCIt synonyms : CD232; Plexin C1 wt Allele; VESPR; PLXN-C1;

NCIt definition : Human PLXNC1 wild-type allele is located in the vicinity of 12q23.3 and is approximately 159 kb in length. This allele, which encodes plexin-C1 protein, plays a role in semaphorin-dependent signaling leading to cytoskeletal remodeling.;

GenBank Accession Number : AF030339;

Details

Origin ID

C113626;

UMLS CUI

C3812284;

Automatic exact mappings (from CISMeF team)
- Plexin c1 [OMIM gene]
OMIM relation
- Plexin c1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_is_element_in_pathway
- Axon Guidance Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Keyword's position in hierarchy(ies) :

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