PRKCG wt Allele

Preferred Label : PRKCG wt Allele;

NCIt synonyms : Protein Kinase C, Gamma wt Allele; SCA14; PKCC; PKCG; MGC57564;

NCIt definition : Human PRKCG wild-type allele is located in the vicinity of 19q13.4 and is approximately 28 kb in length. This allele, which encodes Protein kinase C gamma type protein, plays a role in the regulation of cellular signaling pathways. Mutations in this gene are associated with spinocerebellar ataxia 14.;

GenBank Accession Number : NM_002739;

Details

Origin ID

C111836;

UMLS CUI

C3811241;

Automatic exact mappings (from CISMeF team)
- Protein kinase C, gamma [OMIM gene]
- Spinocerebellar ataxia type 14 [ORDO Disease]
- Spinocerebellar ataxia type 14 (disorder) [SNOMED CT concept]
- protein kinase C gamma [ORDO Gene]
OMIM relation
- Protein kinase C, gamma [OMIM gene]
See also inter- (CISMeF)
- Spinocerebellar ataxia 14 [OMIM Phenotype]
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_plays_role_in_process
- Phosphorylation Process [NCIt concept]
- Serine/Threonine Phosphorylation [NCIt concept]
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients