ENSMUSG00000040112


Mus musculus

Features
Gene ID: ENSMUSG00000040112
  
Biological name :Mrps35
  
Synonyms : mitochondrial ribosomal protein S35 / Mrps35
  
Possible biological names infered from orthology : P82673
  
Species: Mus musculus
  
Chr. number: 6
Strand: 1
Band: G3
Gene start: 147042764
Gene end: 147073991
  
Corresponding Affymetrix probe sets: 10542824 (MoGene1.0st)   1452111_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000048348
Ensembl peptide - ENSMUSP00000144920
NCBI entrez gene - 232536     See in Manteia.
MGI - MGI:2385255
RefSeq - XM_006507035
RefSeq - XM_017321561
RefSeq - NM_145573
RefSeq - XM_006507037
RefSeq Peptide - NP_663548
swissprot - A0A0R4J0L6
swissprot - A0A0N4SV23
Ensembl - ENSMUSG00000040112
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mrps35ENSDARG00000038456Danio rerio
 MRPS35ENSGALG00000036730Gallus gallus
 MRPS35ENSG00000061794Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR019349  Ribosomal protein S24/S35, mitochondrial, conserved domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
No match


Pathways (from Reactome)
Pathway description
Mitochondrial translation elongation
Mitochondrial translation termination


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0002896 abnormal bone mineralization "defect in the process by which minerals are deposited into bone" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hprttm1a(EUCOMM)Hmgu/Hprttm1a(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Hprttm1a(EUCOMM)Hmgu/Ieg

 MP:0003795 abnormal bone structure 
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Allelic Composition: Hprttm1a(EUCOMM)Hmgu/Hprttm1a(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Hprttm1a(EUCOMM)Hmgu/Ieg

 MP:0005553 increased circulating creatinine level "greater than the normal blood concentration of this product of creatine catabolism; abnormal levels indicative of renal dysfunction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]
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Allelic Composition: Hprttm1a(EUCOMM)Hmgu/Hprttm1a(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Hprttm1a(EUCOMM)Hmgu/Ieg

  


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






 

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