ENSMUSG00000039128


Mus musculus

Features
Gene ID: ENSMUSG00000039128
  
Biological name :Cdc123
  
Synonyms : Cdc123 / Cell division cycle / Q8CII2
  
Possible biological names infered from orthology : cell division cycle 123 / O75794
  
Species: Mus musculus
  
Chr. number: 2
Strand: -1
Band: A1
Gene start: 5794294
Gene end: 5845164
  
Corresponding Affymetrix probe sets: 10479869 (MoGene1.0st)   1416763_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000043033
Ensembl peptide - ENSMUSP00000141306
NCBI entrez gene - 98828     See in Manteia.
MGI - MGI:2138811
RefSeq - XM_006497566
RefSeq - NM_133837
RefSeq - XM_006497564
RefSeq - XM_006497565
RefSeq Peptide - NP_598598
swissprot - A0A0A6YVX4
swissprot - Q8CII2
Ensembl - ENSMUSG00000039128
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 cdc123ENSDARG00000075025Danio rerio
 CDC123ENSGALG00000014038Gallus gallus
 CDC123ENSG00000151465Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR009772  Cell division cycle protein 123


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006417 regulation of translation IBA
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0007050 cell cycle arrest IBA
 biological_processGO:0051301 cell division IEA
 cellular_componentGO:0005737 cytoplasm IBA
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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]
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Allelic Composition: Cbx2tm1b(KOMP)Wtsi/Cbx2+
Genetic Background: C57BL/6N-Cbx2tm1b(KOMP)Wtsi/H

 MP:0002075 abnormal coat color "irregular or unusual pigmentation pattern of the hair in relation to control animals" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cbx2tm1b(KOMP)Wtsi/Cbx2+
Genetic Background: C57BL/6N-Cbx2tm1b(KOMP)Wtsi/H

 MP:0002792 abnormal retinal vascularization "malformation or disorganization of the blood vessels supplying the retina" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Cbx2tm1b(KOMP)Wtsi/Cbx2+
Genetic Background: C57BL/6N-Cbx2tm1b(KOMP)Wtsi/H

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
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Allelic Composition: Cbx2tm1b(KOMP)Wtsi/Cbx2+
Genetic Background: C57BL/6N-Cbx2tm1b(KOMP)Wtsi/H

  


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






 

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