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Protein Coding Gene : Cecr2 CECR2, histone acetyl-lysine reader
Primary Identifier  MGI:1923799 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  330409
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable ATP-dependent chromatin remodeler activity. Acts upstream of or within inner ear development; primary neural tube formation; and single fertilization. Part of ISWI-type complex and euchromatin. Is expressed in several structures, including extraembryonic component; genitourinary system; and olfactory epithelium. Used to study anencephaly. Orthologous to human CECR2 (CECR2 histone acetyl-lysine reader).
PHENOTYPE: Homozygous mutant mice display varied penetrance of exencephaly depending on genetic background. [provided by MGI curators]
  • synonyms:
  • gene trap locus 4,
  • MGI:1913831,
  • Gtl4,
  • 2810409N01Rik,
  • RIKEN cDNA 2610101O16 gene,
  • mKIAA1740,
  • MGI:1309479,
  • cat eye syndrome chromosome region, candidate 2,
  • RIKEN cDNA 2810409N01 gene,
  • Cecr2,
  • 2610101O16Rik,
  • CECR2, histone acetyl-lysine reader
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