FGA wt Allele - CISMeF

Preferred Label : FGA wt Allele;

NCIt synonyms : Fib2; Fibrinogen Alpha Chain wt Allele; Fibrinogen, A Alpha Polypeptide Gene; Fibrinogen--Alpha Polypeptide Chain Gene;

NCIt definition : Human FGA wild-type allele is located in the vicinity of 4q31.3 and is approximately 8 kb in length. This allele, which encodes fibrinogen alpha chain protein, plays a role in blood clotting. Mutation of the gene is associated with congenital afibrinogenemia, familial visceral amyloidosis, congenital dysfibrinogenemia and congenital hypodysfibrinogenemia.;

NCI Metathesaurus CUI : CL551944;

GenBank Accession Number : NM_000508;

Détails

Origin ID

C150228;

UMLS CUI

C4723684;

Automatic exact mappings (from CISMeF team)
- Protocadherin-gamma, subfamily b, member 4 [OMIM gene]
OMIM relation
- Fibrinogen, a alpha polypeptide [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_is_element_in_pathway
- Acute Myocardial Infarction Pathway [NCIt concept]
- Complement and Coagulation Cascade [NCIt concept]
- Extrinsic Prothrombin Activation Pathway [NCIt concept]
- Intrinsic Prothrombin Activation Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Cell Growth [NCIt concept]
- Cell Movement [NCIt concept]
- Cell-Matrix Adhesion Process [NCIt concept]
- Coagulation Process [NCIt concept]
- Morphogenesis [NCIt concept]
- Organogenesis [NCIt concept]
- Platelet Activation [NCIt concept]
- Platelet Aggregation Process [NCIt concept]
- Wound Repair [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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