Cell Senescence Entries for PRODH

Cell Types
Foreskin fibroblast, Osteosarcoma
Cell Lines
HS68, U2OS
Cancer Cell?
Yes
Method
Overexpression
Type of senescence
Unclear
Senescence Effect
Induces
Primary Reference
Nagano et al. (2018) Identification of cellular senescence-specific genes by comparative transcriptomics. Sci Rep 6(2)31758 (PubMed)

PRODH Gene Information

HGNC symbol
PRODH 
Aliases
HSPOX2; PIG6; PRODH1; PRODH2; TP53I6 
Common name
proline dehydrogenase 1 
Entrez Id
5625
Description
This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010].

PRODH Ontologies

Gene Ontology
Process: GO:6560; proline metabolic process
GO:6562; proline catabolic process
GO:10133; proline catabolic process to glutamate
GO:8631; intrinsic apoptotic signaling pathway in response to oxidative stress
GO:10942; positive regulation of cell death
GO:19470; 4-hydroxyproline catabolic process
Cellular component: GO:43231; intracellular membrane-bounded organelle
GO:5654; nucleoplasm
GO:5739; mitochondrion
GO:5759; mitochondrial matrix
GO:5743; mitochondrial inner membrane
Function: GO:16491; oxidoreductase activity
GO:4657; proline dehydrogenase activity
GO:71949; FAD binding
Hide GO terms

Homologs of PRODH in Model Organisms

Caenorhabditis elegans
B0513.5
Danio rerio
LOC100537991
Drosophila melanogaster
slgA
Mus musculus
Prodh
Rattus norvegicus
Prodh

External links

OMIM
606810
Ensembl
ENSG00000100033
Entrez Gene
5625
UniGene
517352
1000 Genomes
1000 Genomes
HPRD
GenAtlas
PRODH
GeneCards
PRODH