ENSMUSG00000022307


Mus musculus

Features
Gene ID: ENSMUSG00000022307
  
Biological name :Oxr1
  
Synonyms : Mus musculus oxidation resistance 1 (Oxr1), transcript variant 8, mRNA. / Oxr1 / Q4KMM3
  
Possible biological names infered from orthology : oxidation resistance 1 / Q8N573
  
Species: Mus musculus
  
Chr. number: 15
Strand: 1
Band: B3.1
Gene start: 41447482
Gene end: 41861048
  
Corresponding Affymetrix probe sets: 10423921 (MoGene1.0st)   1418501_a_at (Mouse Genome 430 2.0 Array)   1418502_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000155473
Ensembl peptide - ENSMUSP00000155424
Ensembl peptide - ENSMUSP00000155630
Ensembl peptide - ENSMUSP00000022918
Ensembl peptide - ENSMUSP00000087553
Ensembl peptide - ENSMUSP00000087554
Ensembl peptide - ENSMUSP00000105926
Ensembl peptide - ENSMUSP00000126266
Ensembl peptide - ENSMUSP00000130456
Ensembl peptide - ENSMUSP00000136923
Ensembl peptide - ENSMUSP00000155004
Ensembl peptide - ENSMUSP00000155043
Ensembl peptide - ENSMUSP00000155161
Ensembl peptide - ENSMUSP00000155237
Ensembl peptide - ENSMUSP00000155381
NCBI entrez gene - 170719     See in Manteia.
MGI - MGI:2179326
RefSeq - XM_017316491
RefSeq - NM_001130165
RefSeq - NM_001130166
RefSeq - NM_001358977
RefSeq - NM_001358978
RefSeq - NM_130885
RefSeq - XM_006520524
RefSeq - XM_006520526
RefSeq - XM_006520527
RefSeq - XM_006520531
RefSeq - XM_017316490
RefSeq - NM_001130163
RefSeq - NM_001130164
RefSeq Peptide - NP_001123636
RefSeq Peptide - NP_001123637
RefSeq Peptide - NP_001123638
RefSeq Peptide - NP_001345906
RefSeq Peptide - NP_001345907
RefSeq Peptide - NP_570955
RefSeq Peptide - NP_001123635
swissprot - B1H3M0
swissprot - E9Q0A7
swissprot - Q4KMM3
Ensembl - ENSMUSG00000022307
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 oxr1bENSDARG00000063310Danio rerio
 OXR1ENSGALG00000042182Gallus gallus
 OXR1ENSG00000164830Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Ncoa7 / Q6DFV7 / nuclear receptor coactivator 7 / Q8NI08*ENSMUSG0000003969738
Tldc2 / A2ACG1 / TLD domain-containing protein 2 / A0PJX2* / TBC/LysM-associated domain containing 2*ENSMUSG0000007462812
Tldc1 / Q8K0P3 / TLD domain-containing protein 1 / Q6P9B6* / TBC/LysM-associated domain containing 1*ENSMUSG000000341059


Protein motifs (from Interpro)
Interpro ID Name
 IPR006571  TLDc domain
 IPR018392  LysM domain
 IPR036779  LysM domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007628 adult walking behavior IMP
 biological_processGO:0043524 negative regulation of neuron apoptotic process IMP
 biological_processGO:0051402 neuron apoptotic process IMP
 biological_processGO:0055114 oxidation-reduction process IEA
 biological_processGO:0071447 cellular response to hydroperoxide IMP
 biological_processGO:1900408 negative regulation of cellular response to oxidative stress IDA
 biological_processGO:1902083 negative regulation of peptidyl-cysteine S-nitrosylation IDA
 biological_processGO:1903204 negative regulation of oxidative stress-induced neuron death IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm ISO
 cellular_componentGO:0005730 nucleolus IEA
 cellular_componentGO:0005739 mitochondrion IDA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle ISO
 molecular_functionGO:0016491 oxidoreductase activity IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
Show

Allelic Composition: Whrntm1b(EUCOMM)Wtsi/Whrntm1b(EUCOMM)Wtsi
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6N

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Whrntm1b(EUCOMM)Wtsi/Whrntm1b(EUCOMM)Wtsi
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6N

 MP:0002229 CNS neurodegeneration "a retrogressive impairment of function or destruction of neural tissue" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Whrntm1b(EUCOMM)Wtsi/Whrntm1b(EUCOMM)Wtsi
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6N

 MP:0003203 increased neuron apoptosis "increase in the number of neurons undergoing programmed cell death" [RGD:Rat Genome Database submission]
Show

Allelic Composition: Whrntm1b(EUCOMM)Wtsi/Whrntm1b(EUCOMM)Wtsi
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6N

  


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






 

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