CHGB wt Allele

Preferred Label : CHGB wt Allele;

NCIt synonyms : CGB Gene; CHGB; Chromogranin B (Secretogranin 1) wt Allele; SCG1 Gene;

NCIt definition : Human CHGB wild-type allele is located within 20pter-p12 and is approximately 14 kb in length. This allele, which encodes secretogranin-1 protein, is involved in the regulation of interactions between the nervous and endocrine systems.;

GenBank Accession Number : NM_001819;

Details

Origin ID

C52405;

UMLS CUI

C1706045;

Automatic exact mappings (from CISMeF team)
- Chromogranin b [OMIM gene]
OMIM relation
- Chromogranin b [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_associated_with_disease
- Adrenal Gland Pheochromocytoma [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 20: 5840168-5854003 [NCIt concept]
gene_in_chromosomal_location
- 20pter-p12 [NCIt concept]
gene_plays_role_in_process
- Intercellular Communication Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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