C3 wt Allele - CISMeF

Preferred Label : C3 wt Allele;

NCIt synonyms : Complement Component 3 wt Allele; CPAMD1;

NCIt definition : Human C3 wild-type allele is located within 19p13.3-p13.2 and is approximately 43 kb in length. This allele, which encodes complement C3 protein, plays a critical role in the activation of complement system.;

GenBank Accession Number : NM_000064;

Details

Origin ID

C49550;

UMLS CUI

C1707067;

Automatic exact mappings (from CISMeF team)
- complement C3 [ORDO Gene]
OMIM relation
- Complement component 3 [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_associated_with_disease
- C3 Deficiency [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 19: 6671660-6628878 [NCIt concept]
gene_in_chromosomal_location
- 19p13.3-p13.2 [NCIt concept]
gene_is_element_in_pathway
- Alternative Complement Pathway [NCIt concept]
- Classical Complement Pathway [NCIt concept]
- Complement Pathway [NCIt concept]
- Lectin Induced Complement Pathway [NCIt concept]
- Local Acute Inflammatory Response Pathway [NCIt concept]
gene_plays_role_in_process
- Complement Activation [NCIt concept]
- Host Defense Mechanism [NCIt concept]

Keyword's position in hierarchy(ies) :

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