HSP90B2P wt Allele

Preferred Label : HSP90B2P wt Allele;

NCIt synonyms : Tumor Rejection Antigen (Gp96) Pseudogene 1; TRA1P1; Tumor Rejection Antigen (Gp96) 1 Pseudogene 1; HSPCP2; GRP94P1; GRP94B; Heat Shock Protein 90kDa Beta (Grp94), Member 2, Pseudogene wt Allele; TRAP1; HSP;

NCIt definition : Human HSP90B2P wild-type allele is located in the vicinity of 15q26.3 and is approximately 3 kb in length. This allele, which may encode putative endoplasmin-like protein, may be involved in protein folding.;

NCIt note : Both HGNC and EntrezGene categorize the HSP90B2P gene as a pseudogene, which implies that no protein product is produced. However, there is a UniProt entry for a potential protein product, putative endoplasmin-like protein.;

GenBank Accession Number : AY956768;

Details

Origin ID

C116983;

UMLS CUI

C3890018;

Automatic exact mappings (from CISMeF team)
- Hereditary spastic paraplegia [ORDO Disease]
- Transforming growth factor-beta receptor-associated protein 1 [OMIM gene]
- Tumor necrosis factor receptor-associated protein 1 [OMIM gene]
- spastic paraplegia, hereditary [MeSH Descriptor]
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
- 15q26.3 [NCIt concept]
gene_plays_role_in_process
- Protein Folding [NCIt concept]
- Subcellular Protein Targeting [NCIt concept]
- Unfolded Protein Response [NCIt concept]

Keyword's position in hierarchy(ies) :

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