PPIF wt Allele

Preferred Label : PPIF wt Allele;

NCIt synonyms : Cyp-D; CYP3; CyP-M; Peptidylprolyl Isomerase F wt Allele; Peptidylprolyl Isomerase F (Cyclophilin F) Gene; CypD;

NCIt definition : Human PPIF wild-type allele is located within 10q22-q23 and is approximately 8 kb in length. This allele, which encodes peptidyl-prolyl cis-trans isomerase F, mitochondrial protein, plays a role in the modulation of both protein folding and mitochondrial permeability transition pore-induced cell death.;

GenBank Accession Number : M80254;

Details

Origin ID

C118235;

UMLS CUI

C3890897;

Automatic exact mappings (from CISMeF team)
- Cytochrome p450, subfamily iiia, polypeptide 4 [OMIM gene]
- Peptidyl-prolyl cis/trans isomerase, mitochondrial [OMIM gene]
- Peptidyl-prolyl isomerase D [OMIM gene]
OMIM relation
- Peptidyl-prolyl cis/trans isomerase, mitochondrial [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 10q22-q23 [NCIt concept]
gene_is_element_in_pathway
- Calcium-Mediated Signaling Pathway [NCIt concept]
- Huntington's Disease Pathway [NCIt concept]
- Parkinson's Disease Pathway KEGG [NCIt concept]
gene_plays_role_in_process
- Negative Regulation of Apoptosis [NCIt concept]
- Positive Regulation of Necrotic Process [NCIt concept]
- Protein Folding [NCIt concept]

Keyword's position in hierarchy(ies) :

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