GC wt Allele - CISMeF

Preferred Label : GC wt Allele;

NCIt synonyms : VDBG; DBP; Group-Specific Component (Vitamin D Binding Protein) wt Allele; GC; VDBP; Gc-MAF; GRD3; HEL-S-51; DBP/GC; GcMAF;

NCIt definition : Human GC wild-type allele is located within 4q12-q13 and is approximately 42 kb in length. This allele, which encodes vitamin D-binding protein, is involved in the transport of vitamin D and its metabolites to targeted tissues.;

NCIt note : Over 80 variants of the human GC gene have been identified. The three most common alleles are called GC*1F, GC*1S, and GC*2. (SwissProt);

GenBank Accession Number : NM_000583;

Details

Origin ID

C52279;

UMLS CUI

C1704663;

False automatic mappings
- Group-specific component [OMIM Phenotype]
OMIM relation
- Group-specific component [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 4: 73014923-72972448 [NCIt concept]
gene_in_chromosomal_location
- 4q12-q13 [NCIt concept]
gene_plays_role_in_process
- Ligand Binding [NCIt concept]
- Lipid Metabolic Process [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients