ENSMUSG00000046719


Mus musculus

Features
Gene ID: ENSMUSG00000046719
  
Biological name :Nxph3
  
Synonyms : Neurexophilin-3 / Nxph3 / Q91VX5
  
Possible biological names infered from orthology : O95157
  
Species: Mus musculus
  
Chr. number: 11
Strand: -1
Band: D
Gene start: 95509845
Gene end: 95514570
  
Corresponding Affymetrix probe sets: 10390170 (MoGene1.0st)   1419710_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000058254
NCBI entrez gene - 104079     See in Manteia.
MGI - MGI:1336188
RefSeq - NM_130858
RefSeq Peptide - NP_570928
swissprot - Q544G3
swissprot - Q91VX5
Ensembl - ENSMUSG00000046719
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 nxph3ENSDARG00000070694Danio rerio
 NXPH3ENSGALG00000038645Gallus gallus
 NXPH3ENSG00000182575Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Nxph2 / Q61199 / Neurexophilin-2 / O95156*ENSMUSG0000006913242
Nxph1 / Q61200 / Neurexophilin-1 / P58417*ENSMUSG0000004617842
Nxph4 / neurexophilin 4 / O95158*ENSMUSG0000004025835


Protein motifs (from Interpro)
Interpro ID Name
 IPR010450  Neurexophilin
 IPR026845  Neurexophilin/NXPE


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0005576 extracellular region IEA
 molecular_functionGO:0005102 signaling receptor binding IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001392 abnormal locomotor activity "altered ability or inability to move from place to place" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cdkn1atm1Tyj/Cdkn1atm1Tyj,Tg(MMTV-vHaras)SH1Led/0
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N

 MP:0001405 impaired coordination "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Cdkn1atm1Tyj/Cdkn1atm1Tyj,Tg(MMTV-vHaras)SH1Led/0
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N

 MP:0001463 abnormal spatial learning "defects in the abilibity to navigate using behavioraly meaningful locations" [CFG:Center for Functional Genomics , Northwestern University]
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Allelic Composition: Cdkn1atm1Tyj/Cdkn1atm1Tyj,Tg(MMTV-vHaras)SH1Led/0
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N

 MP:0001488 increased startle reflex "reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn1atm1Tyj/Cdkn1atm1Tyj,Tg(MMTV-vHaras)SH1Led/0
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn1atm1Tyj/Cdkn1atm1Tyj,Tg(MMTV-vHaras)SH1Led/0
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N

  


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






 

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