ENSMUSG00000032381


Mus musculus

Features
Gene ID: ENSMUSG00000032381
  
Biological name :Fam96a
  
Synonyms : Fam96a / MIP18 family protein FAM96A / Q9DCL2
  
Possible biological names infered from orthology : family with sequence similarity 96 member A / Q9H5X1
  
Species: Mus musculus
  
Chr. number: 9
Strand: 1
Band: C
Gene start: 66126611
Gene end: 66138955
  
Corresponding Affymetrix probe sets: 10586484 (MoGene1.0st)   1416633_a_at (Mouse Genome 430 2.0 Array)   1416634_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000034945
NCBI entrez gene - 68250     See in Manteia.
MGI - MGI:1915500
RefSeq - XM_011242805
RefSeq - NM_026635
RefSeq - XM_006511397
RefSeq Peptide - NP_080911
swissprot - Q9DCL2
Ensembl - ENSMUSG00000032381
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 fam96aENSDARG00000104940Danio rerio
 FAM96AENSGALG00000026448Gallus gallus
 FAM96AENSG00000166797Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Fam96b / Q9D187 / Mitotic spindle-associated MMXD complex subunit MIP18 / Q9Y3D0* / family with sequence similarity 96 member B*ENSMUSG0000003187943


Protein motifs (from Interpro)
Interpro ID Name
 IPR002744  MIP18 family-like
 IPR034904  Fe-S cluster assembly domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007059 chromosome segregation IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IEA
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0002966 decreased circulating alkaline phosphatase level "reduced activity of this enzyme, which hydrolyzes orthophosphoric monoesters, found in the blood" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Cbx5tm1a(EUCOMM)Wtsi/Cbx5tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Cbx5tm1a(EUCOMM)Wtsi/Wtsi

 MP:0003047 abnormal thoracic vertebrae morphology "malformation of any or all of the thirteen bony segments of the spine located anterior to the lumbar vertebrae and posterior to the cervical vertebrae" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Cbx5tm1a(EUCOMM)Wtsi/Cbx5tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Cbx5tm1a(EUCOMM)Wtsi/Wtsi

 MP:0003345 decreased number of ribs "fewer than normal numbers of the pairs of bony structures that make up the body wall" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Cbx5tm1a(EUCOMM)Wtsi/Cbx5tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Cbx5tm1a(EUCOMM)Wtsi/Wtsi

 MP:0005478 decreased circulating thyroxine level "less than the normal blood concentration of the major hormone dervied from the thryoid gland; it normally affects cellular metabolism" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cbx5tm1a(EUCOMM)Wtsi/Cbx5tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Cbx5tm1a(EUCOMM)Wtsi/Wtsi

 MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number "reduced number of CD8-positive, alpha beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000913, GO_REF:0000031, GOC:add, GOC:pam, PMID:20146720]
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Allelic Composition: Cbx5tm1a(EUCOMM)Wtsi/Cbx5tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Cbx5tm1a(EUCOMM)Wtsi/Wtsi

  


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






 

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