C5 wt Allele - CISMeF

Preferred Label : C5 wt Allele;

NCIt synonyms : C5b Gene; C5D; ECLZB; CPAMD4; Component 5 wt Allele; Complement Component 5 Gene; C5a Gene;

NCIt definition : Human C5 wild-type allele is located within 9q33-q34 and is approximately 98 kb in length. This allele, which encodes complement C5 protein, is involved in the complement system, inflammatory responses, and histamine release.;

GenBank Accession Number : NM_001735;

Details

Origin ID

C49551;

UMLS CUI

C1707068;

Automatic exact mappings (from CISMeF team)
- Complement component 5 deficiency [OMIM Phenotype]
- complement C5 [ORDO Gene]
OMIM relation
- Complement component 5 [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
- C5 Deficiency [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 9: 120892108-120794170 [NCIt concept]
gene_in_chromosomal_location
- 9q32-q34 [NCIt concept]
gene_is_element_in_pathway
- Alternative Complement Pathway [NCIt concept]
- Classical Complement Pathway [NCIt concept]
- Complement Pathway [NCIt concept]
- Granulocyte Adhesion Pathway [NCIt concept]
- Lectin Induced Complement Pathway [NCIt concept]
- Local Acute Inflammatory Response Pathway [NCIt concept]
gene_plays_role_in_process
- Chemotactic Process [NCIt concept]
- Complement Activation [NCIt concept]
- Inflammatory Response [NCIt concept]
- Stress Response Signaling [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients