ENSMUSG00000031231


Mus musculus

Features
Gene ID: ENSMUSG00000031231
  
Biological name :Cox7b
  
Synonyms : Cox7b / Cytochrome c oxidase subunit 7B, mitochondrial / P56393
  
Possible biological names infered from orthology : cytochrome c oxidase subunit 7B / P24311
  
Species: Mus musculus
  
Chr. number: X
Strand: 1
Band: D
Gene start: 106015700
Gene end: 106022450
  
Corresponding Affymetrix probe sets: 10358709 (MoGene1.0st)   10601356 (MoGene1.0st)   
  
Cross references: Ensembl peptide - ENSMUSP00000033582
NCBI entrez gene - 66142     See in Manteia.
MGI - MGI:1913392
RefSeq - NM_025379
RefSeq Peptide - NP_079655
swissprot - P56393
swissprot - Q5FW98
Ensembl - ENSMUSG00000031231
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 cox7bENSDARG00000115557Danio rerio
 COX7BENSGALG00000007863Gallus gallus
 COX7BENSG00000131174Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Cox7b2 / cytochrome c oxidase subunit VIIb2 / Q8TF08* / cytochrome c oxidase subunit 7B2*ENSMUSG0000004938748


Protein motifs (from Interpro)
Interpro ID Name
 IPR008433  Cytochrome C oxidase, subunit VIIB
 IPR023272  Cytochrome C oxidase, subunit VIIB domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007417 central nervous system development IEA
 biological_processGO:0022900 electron transport chain IEA
 biological_processGO:1902600 proton transmembrane transport IEA
 cellular_componentGO:0005739 mitochondrion IDA
 cellular_componentGO:0005743 mitochondrial inner membrane IEA
 cellular_componentGO:0005746 mitochondrial respiratory chain IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0045277 respiratory chain complex IV IBA
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0004129 cytochrome-c oxidase activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0009781 abnormal preimplantation embryo development "an anomaly in the developmental progress of an embryo from 2 cell to blastocyst affecting the viability or number of embryos" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: BcorGt(W096D07)Wrst/Y
Genetic Background: chimera involves: 129S2/SvPas

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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