Full name: chromodomain helicase DNA binding protein 7

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: A730019I05Rik; Cycn; Cyn; Dz; Edy; Flo; GENA 47; GENA 60; Gena 52; Lda; Mt; Obt; Todo; WBE1; Whi; metis

Summary: This gene encodes a protein containing two chromodomains and an ATP-binding helicase domain that functions as a regulator of transcription. Mutations in this gene result in an array of development defects, including inner ear problems. Mice defective for this gene exhibit many of the clinical features of the CHARGE syndrome caused by mutations in the homologous gene in human. [provided by RefSeq, Sep 2015]

Expression: Broad expression in CNS E11.5 (RPKM 14.2), cerebellum adult (RPKM 11.8) and 28 other tissues

Gene size: 178105bp

Exon count: 39