GP9 wt Allele - CISMeF

Preferred Label : GP9 wt Allele;

NCIt synonyms : Glycoprotein IX, Platelet Gene; GPIX; Glycoprotein IX Platelet wt Allele; CD42a; Glycoprotein IX (Platelet) Gene;

NCIt definition : Human GP9 wild-type allele is located in the vicinity of 3q21.3 and is approximately 7 kb in length. This allele, which encodes platelet glycoprotein IX protein, is involved in the regulation of platelet aggregation. Mutation of the gene is associated with Bernard-Soulier syndrome type C.;

NCI Metathesaurus CUI : CL505032;

GenBank Accession Number : NM_000174;

Details

Origin ID

C126553;

UMLS CUI

C4284289;

Automatic exact mappings (from CISMeF team)
- glycoprotein IX platelet [ORDO Gene]
- platelet glycoprotein GPIb-IX complex [MeSH Descriptor]
OMIM relation
- Glycoprotein ix, platelet [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_is_element_in_pathway
- ECM-Receptor Interaction Signaling Pathway [NCIt concept]
- Hematopoietic Cell Lineage Pathway [NCIt concept]
gene_plays_role_in_process
- Ligand Binding [NCIt concept]
- Platelet Activation [NCIt concept]
- Positive Regulation of Platelet Aggregation Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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