Gene: PPIF (peptidylprolyl isomerase F)  Homo sapiens

Symbol: PPIF
Name: peptidylprolyl isomerase F
Description: The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein is part of the mitochondrial permeability transition pore in the inner mitochondrial membrane. Activation of this pore is thought to be involved in the induction of apoptotic and necrotic cell death. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: cyclophilin 3; cyclophilin D; cyclophilin F; Cyp-D; CyP-M; CYP3; CypD; FLJ90798; MGC117207; mitochondrial cyclophilin; OTTHUMP00000019925; OTTHUMP00000019926; peptidyl-prolyl cis-trans isomerase F, mitochondrial; peptidyl-prolyl cis-trans isomerase, mitochondral; peptidyl-prolyl cis-trans isomerase, mitochondrial; PPIase F; rotamase F
Orthologs: Mus musculus : Ppif (peptidylprolyl isomerase F (cyclophilin F))  MGI
Rattus norvegicus : Ppif (peptidylprolyl isomerase F)
Latest Assembly: Human Genome Assembly GRCh37
NCBI Annotation Information: Note: This gene encodes a 178 aa mature peptide that is found in the mitochondrion. It has been labeled 'cyclophilin D'. This same name has also been applied to a different cytoplasmic protein of 370 aa, which is represented by Entrez GeneID 5481, PPID. [10 Oct 2008]
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11081,480,435 - 81,488,305+NCBI
Human Genome Assembly HuRef1075,101,849 - 75,109,719+NCBI
Human Genome Assembly GRCh371081,107,220 - 81,115,090+NCBI
Human Genome Assembly Build 361080,777,226 - 80,785,096+NCBI
Human Cytogenetic Map10q22-q23 NCBI
Human Genome Assembly1080,777,225 - 80,785,093 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on PPIF
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1354243
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-03-19
Status: ACTIVE