AHSG wt Allele

Preferred Label : AHSG wt Allele;

NCIt synonyms : AHS; PRO2743; Feutin, Mouse, Homolog of Gene; Alpha-2-HS-Glycoprotein wt Allele; A2HS; FETUA; HSGA;

NCIt definition : Human AHSG wild-type allele is located in the vicinity of 3q27 and is approximately 8 kb in length. This allele, which encodes alpha-2-HS-glycoprotein, plays a role in the modulation of bone formation.;

GenBank Accession Number : NM_001622;

Details

Origin ID

C113822;

UMLS CUI

C3812154;

Automatic exact mappings (from CISMeF team)
- Alien Limb Phenomenon [MeSH Descriptor]
- Alpha-2-hs-glycoprotein [OMIM gene]
- alpha 2-HS glycoprotein [ORDO Gene]
OMIM relation
- Alpha-2-hs-glycoprotein [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_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 3q27 [NCIt concept]
gene_is_element_in_pathway
- BMP Receptor Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Phagocytosis Induction [NCIt concept]
- Skeletal Development [NCIt concept]

Keyword's position in hierarchy(ies) :

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