Mine Disruption Phenotype

Gene Info

  • Species:Mouse (Mus musculus)
  • GeneID:244059
  • Symbol:Chd2
  • Description:chromodomain helicase DNA binding protein 2
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Gene ID Entry Entry Name Protein Name Type Information
244059 E9PZM4 CHD2_MOUSE Chromodomain-helicase-DNA-binding protein 2 (CHD-2) (EC 3.6.4.12) (ATP-dependent helicase CHD2) DISRUPTION PHENOTYPE Growth delay late in embryogenesis and perinatal lethality (PubMed:16810678). Heterozygous mice show decreased neonatal viability. Heterozygous mice display glomerulopathy, proteinuria and impaired kidney function. Glomerulopathy may be associated with anemia (PubMed:19142019). Heterozygous mutant also show increased extramedullary hematopoiesis and susceptibility to lymphomas, with defects in hematopoietic stem cell differentiation (PubMed:19137022). {ECO:0000269|PubMed:16810678, ECO:0000269|PubMed:19137022, ECO:0000269|PubMed:19142019}.