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Protein Coding Gene : Kdm2a lysine (K)-specific demethylase 2A

Primary Identifier  MGI:1354736 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  225876
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables unmethylated CpG binding activity. Involved in transcription initiation-coupled chromatin remodeling. Acts upstream of or within several processes, including epithelial tube morphogenesis; neuroepithelial cell differentiation; and regulation of gene expression. Part of chromatin. Is expressed in embryo; forebrain; and limb. Human ortholog(s) of this gene implicated in lung non-small cell carcinoma. Orthologous to human KDM2A (lysine demethylase 2A).
PHENOTYPE: Mice homozygous for a null allele show embryonic lethality, severe growth retardation, reduced neuron proliferation, increased neuron apoptosis, impaired neuron differentiation, small hearts, abnormal cardiac looping and, in some cases, incomplete embryonic turning and neural tube closure defects. [provided by MGI curators]
  • synonyms:
  • Cxxc8,
  • Gm4560,
  • AW536790,
  • lysine (K)-specific demethylase 2A,
  • expressed sequence AW536790,
  • F-box and leucine-rich repeat protein 11,
  • AA589516,
  • Kdm2a,
  • RIKEN cDNA 5530401A10 gene,
  • 100043628,
  • Fbxl11,
  • lalina,
  • Fbl7,
  • predicted gene 4560,
  • Jhdm1a,
  • MGI:2147454,
  • expressed sequence AA589516,
  • MGI:2147738,
  • MGI:3782744,
  • predicted gene, 100043628,
  • 5530401A10Rik,
  • MGI:1918681

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