HPR wt Allele - CISMeF

Preferred Label : HPR wt Allele;

NCIt synonyms : HP; Haptoglobin-Related Protein wt Allele; A-259H10.2;

NCIt definition : Human HPR wild-type allele is located in the vicinity of 16q22.1 and is approximately 3 kb in length. This allele, which encodes haptoglobin-related protein, plays a role in the binding of antibodies produced in response to Trypanosome brucei.;

GenBank Accession Number : NM_020995;

Details

Origin ID

C54286;

UMLS CUI

C1705568;

Automatic exact mappings (from CISMeF team)
- Haptoglobin [OMIM gene]
- Hypersensitivity pneumonitis [ORDO Disease]
- Pancreatitis, hereditary [OMIM Phenotype]
- helicobacter pylori [MeSH Descriptor]
- hermanski-pudlak syndrome [MeSH Descriptor]
- hospitals, psychiatric [MeSH Descriptor]
- pituitary gland [UBERON concept]
OMIM relation
- Haptoglobin-related protein [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 16: 70665292-70668646 [NCIt concept]
gene_in_chromosomal_location
- 16q22.1 [NCIt concept]
gene_is_biomarker_type
- Prognostic Marker [NCIt concept]
gene_plays_role_in_process
- Hydrolysis [NCIt concept]
- Immune Response Process [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Proteolysis [NCIt concept]

Keyword's position in hierarchy(ies) :

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