ENSG00000100033


Homo sapiens

Features
Gene ID: ENSG00000100033
  
Biological name :PRODH
  
Synonyms : O43272 / PRODH / proline dehydrogenase 1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: -1
Band: q11.21
Gene start: 18912777
Gene end: 18936553
  
Corresponding Affymetrix probe sets: 214203_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000396806
Ensembl peptide - ENSP00000480347
Ensembl peptide - ENSP00000413941
Ensembl peptide - ENSP00000410805
Ensembl peptide - ENSP00000409742
Ensembl peptide - ENSP00000334726
Ensembl peptide - ENSP00000349577
NCBI entrez gene - 5625     See in Manteia.
OMIM - 606810
RefSeq - NM_001195226
RefSeq - NM_016335
RefSeq Peptide - NP_001182155
RefSeq Peptide - NP_057419
swissprot - E7EQL6
swissprot - O43272
swissprot - C9JIW4
swissprot - A0A087WWM6
swissprot - H7C363
swissprot - H7C3U9
Ensembl - ENSG00000100033
  
Related genetic diseases (OMIM): 239500 - Hyperprolinemia, type I, 239500
  600850 - {Schizophrenia, susceptibility to, 4}, 600850
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 prodhaENSDARG00000086746Danio rerio
 prodhbENSDARG00000086512Danio rerio
 ENSGALG00000007728Gallus gallus
 ProdhENSMUSG00000003526Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PRODH2 / Q9UF12 / proline dehydrogenase 2ENSG0000025079931


Protein motifs (from Interpro)
Interpro ID Name
 IPR002872  Proline dehydrogenase domain
 IPR015659  Proline oxidase family
 IPR029041  FAD-linked oxidoreductase-like


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006560 proline metabolic process IEA
 biological_processGO:0006562 proline catabolic process IEA
 biological_processGO:0008631 intrinsic apoptotic signaling pathway in response to oxidative stress NAS
 biological_processGO:0010133 proline catabolic process to glutamate IEA
 biological_processGO:0010942 positive regulation of cell death IDA
 biological_processGO:0019470 4-hydroxyproline catabolic process TAS
 biological_processGO:0055114 oxidation-reduction process IEA
 cellular_componentGO:0005739 mitochondrion IBA
 cellular_componentGO:0005743 mitochondrial inner membrane TAS
 cellular_componentGO:0005759 mitochondrial matrix IEA
 molecular_functionGO:0004657 proline dehydrogenase activity IEA
 molecular_functionGO:0016491 oxidoreductase activity IEA
 molecular_functionGO:0071949 FAD binding IDA


Pathways (from Reactome)
Pathway description
Proline catabolism


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000093 Proteinuria 
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 HP:0000112 Nephropathy "A nonspecific term referring to disease or damage of the kidneys." [HPO:curators]
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 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0000733 Stereotyped, repetitive behaviour 
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 HP:0000752 Hyperactivity 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0002133 Status epilepticus 
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 HP:0002353 EEG abnormalities "Abnormality observed by electroencephalogram (EEG), which is used to record of the brain s spontaneous electrical activity from multiple electrodes placed on the scalp." [HPO:curators]
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 HP:0003080 Hydroxyprolinuria 
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 HP:0003108 Hyperglycinuria 
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 HP:0003137 Prolinuria 
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 HP:0003812 Phenotypic variability 
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 HP:0008358 Hyperprolinemia 
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 HP:0100753 Schizophrenia "A mental disorder characterized by a disintegration of thought processes and of emotional responsiveness. It most commonly manifests as auditory hallucinations, paranoid or bizarre delusions, or disorganized speech and thinking, and it is accompanied by significant social or occupational dysfunction. The onset of symptoms typically occurs in young adulthood, with a global lifetime prevalence of about 0.3-0.7%." [HPO:sdoelken]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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