HP wt Allele - CISMeF

Preferred Label : HP wt Allele;

NCIt synonyms : Haptoglobin wt Allele; BP; HPA1S; HP2ALPHA2;

NCIt definition : Human HP wild-type allele is located in the vicinity of 16q22.1 and is approximately 6 kb in length. This allele, which encodes haptoglobin protein, is involved in both the prevention of iron loss in the kidney and in the protection of damage in the kidney.;

GenBank Accession Number : NM_005143;

Details

Origin ID

C51250;

UMLS CUI

C1708288;

Automatic exact mappings (from CISMeF team)
- 4-(benzyloxy)-2,6-diamino-5-nitropyrimidine [MeSH Supplementary Concept]
- Arterial pressure monitoring, non-invasive method (regime/therapy) [SNOMED CT concept]
- Haptoglobin [OMIM gene]
- Heparanase [OMIM gene]
- NO-BP [MeSH concept]
- bicycle-pedal (BP) mechanism [IUPAC Term]
- diphosphonates [MeSH Descriptor]
- pemphigoid, bullous [MeSH Descriptor]
OMIM relation
- Haptoglobin [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 16: 70646027-70652455 [NCIt concept]
gene_in_chromosomal_location
- 16q22.1 [NCIt concept]
gene_plays_role_in_process
- Ligand Binding [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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