PLXND1 wt Allele

Preferred Label : PLXND1 wt Allele;

NCIt synonyms : Plexin D1 wt Allele; PLEXD1; KIAA0620;

NCIt definition : Human PLXND1 wild-type allele is located in the vicinity of 3q22.1 and is approximately 52 kb in length. This allele, which encodes plexin-D1 protein, plays a role in semaphorin-mediated signaling.;

NCIt note : There is a report of a chromosomal aberration involving the PLXND1 gene and the TMCC1 gene, which is associated with breast cancer. (COSMIC);

GenBank Accession Number : AY116661;

Details

Origin ID

C114411;

UMLS CUI

C3815264;

Automatic exact mappings (from CISMeF team)
- plexin D1 [ORDO Gene]
OMIM relation
- Plexin d1 [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_in_chromosomal_location
- 3q22.1 [NCIt concept]
gene_plays_role_in_process
- Angiogenic Process [NCIt concept]
- Cellular Migration Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Keyword's position in hierarchy(ies) :

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