ENSMUSG00000045349


Mus musculus

Features
Gene ID: ENSMUSG00000045349
  
Biological name :Sh2d5
  
Synonyms : Q8JZW5 / Sh2d5 / SH2 domain-containing protein 5
  
Possible biological names infered from orthology : Q6ZV89 / SH2 domain containing 5
  
Species: Mus musculus
  
Chr. number: 4
Strand: 1
Band: D3
Gene start: 138250403
Gene end: 138261332
  
Corresponding Affymetrix probe sets: 10509514 (MoGene1.0st)   1436100_at (Mouse Genome 430 2.0 Array)   1439434_x_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000101449
Ensembl peptide - ENSMUSP00000119052
Ensembl peptide - ENSMUSP00000101450
NCBI entrez gene - 230863     See in Manteia.
MGI - MGI:2446215
RefSeq - NM_001099631
RefSeq Peptide - NP_001093101
swissprot - A2AM67
swissprot - A2AM66
swissprot - Q8JZW5
Ensembl - ENSMUSG00000045349
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 sh2d5ENSDARG00000014324Danio rerio
 SH2D5ENSGALG00000044997Gallus gallus
 SH2D5ENSG00000189410Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR000980  SH2 domain
 IPR006020  PTB/PI domain
 IPR011993  PH-like domain superfamily
 IPR036860  SH2 domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0008150 biological_process ND
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0014069 postsynaptic density IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030054 cell junction IEA
 cellular_componentGO:0045202 synapse IEA
 cellular_componentGO:0045211 postsynaptic membrane IEA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0005554 decreased circulating creatinine level "less 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: Rpgrip1ltm1a(EUCOMM)Wtsi/Rpgrip1ltm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Rpgrip1ltm1a(EUCOMM)Wtsi/Wtsi

  


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






 

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