ENSMUSG00000034875


Mus musculus

Features
Gene ID: ENSMUSG00000034875
  
Biological name :Nudt19
  
Synonyms : Nucleoside diphosphate-linked moiety X motif 19 / Nudt19 / P11930
  
Possible biological names infered from orthology : A8MXV4 / nudix hydrolase 19
  
Species: Mus musculus
  
Chr. number: 7
Strand: -1
Band: B2
Gene start: 35547185
Gene end: 35556304
  
Corresponding Affymetrix probe sets: 10562480 (MoGene1.0st)   1432332_a_at (Mouse Genome 430 2.0 Array)   1434216_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000047778
NCBI entrez gene - 110959     See in Manteia.
MGI - MGI:94203
RefSeq - NM_033080
RefSeq Peptide - NP_149071
swissprot - P11930
Ensembl - ENSMUSG00000034875
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 nudt19ENSDARG00000077537Danio rerio
 NUDT19ENSGALG00000029498Gallus gallus
 A8MXV4ENSG00000213965Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR000086  NUDIX hydrolase domain
 IPR015797  NUDIX hydrolase-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0005739 mitochondrion IDA
 cellular_componentGO:0005777 peroxisome IEA
 molecular_functionGO:0005102 signaling receptor binding IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Peroxisomal lipid metabolism
Peroxisomal protein import


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000266 abnormal cardiac morphology "anomalies in the hollow, muscular organ that maintains the circulation of the blood" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Ncoa3tm1b(EUCOMM)Wtsi/Ncoa3+
Genetic Background: C57BL/6N-Ncoa3tm1b(EUCOMM)Wtsi/H

 MP:0000274 enlarged heart "increase over normal size of the heart" [J:29971]
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Allelic Composition: Ncoa3tm1b(EUCOMM)Wtsi/Ncoa3+
Genetic Background: C57BL/6N-Ncoa3tm1b(EUCOMM)Wtsi/H

 MP:0002060 abnormal skin morphology "malformation or atypical structure of the membranous protective covering of the body" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:56777]
Show

Allelic Composition: Ncoa3tm1b(EUCOMM)Wtsi/Ncoa3+
Genetic Background: C57BL/6N-Ncoa3tm1b(EUCOMM)Wtsi/H

  


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






 

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