ENSG00000164405


Homo sapiens

Features
Gene ID: ENSG00000164405
  
Biological name :UQCRQ
  
Synonyms : O14949 / ubiquinol-cytochrome c reductase complex III subunit VII / UQCRQ
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 5
Strand: 1
Band: q31.1
Gene start: 132866560
Gene end: 132868031
  
Corresponding Affymetrix probe sets: 201568_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000367936
Ensembl peptide - ENSP00000367939
Ensembl peptide - ENSP00000367934
NCBI entrez gene - 27089     See in Manteia.
OMIM - 612080
RefSeq - NM_014402
RefSeq Peptide - NP_055217
swissprot - O14949
Ensembl - ENSG00000164405
  
Related genetic diseases (OMIM): 615159 - Mitochondrial complex III deficiency, nuclear type 4, 615159
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
 uqcrqENSDARG00000029064Danio rerio
 UQCRQENSGALG00000028302Gallus gallus
 UqcrqENSMUSG00000044894Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR004205  Cytochrome b-c1 complex subunit 8
 IPR036642  Cytochrome b-c1 complex subunit 8 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006122 mitochondrial electron transport, ubiquinol to cytochrome c TAS
 biological_processGO:0021539 subthalamus development IEA
 biological_processGO:0021548 pons development IEA
 biological_processGO:0021680 cerebellar Purkinje cell layer development IEA
 biological_processGO:0021766 hippocampus development IEA
 biological_processGO:0021794 thalamus development IEA
 biological_processGO:0021854 hypothalamus development IEA
 biological_processGO:0021860 pyramidal neuron development IEA
 biological_processGO:0030901 midbrain development IEA
 biological_processGO:0055114 oxidation-reduction process IEA
 cellular_componentGO:0005739 mitochondrion IEA
 cellular_componentGO:0005743 mitochondrial inner membrane TAS
 cellular_componentGO:0005750 mitochondrial respiratory chain complex III IBA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0070469 respiratory chain IEA
 molecular_functionGO:0008121 ubiquinol-cytochrome-c reductase activity IBA


Pathways (from Reactome)
Pathway description
Respiratory electron transport


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:0001251 Ataxia "Ataxia is a nonspecific neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is caused by dysfunction of one or more parts of the nervous system including the cerebellum, the sensory nervous system, the vestibular system, or the cerebral cortex." [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:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0001344 Absent speech development 
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0002071 Extrapyramidal signs 
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 HP:0002151 Increased serum lactate "Abnormally increased level of blood lactate (2-hydroxypropanoic acid). Lactate is produced from pyruvate by lactate dehydrogenase during normal metabolism." [HPO:curators]
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 HP:0002305 Athetosis "Athetosis (from the Greek word for changeable or unfixed ) refers to an inability to sustain the muscles of the fingers, toes, tongue, or any other group of muscles in a fixed position. Instead, posture is interrupted by slow, purposeless involuntary movements." [HPO:curators]
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 HP:0010864 Mental retardation, severe "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 20-34." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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