Synonyms:CHD7, CRG, ENTREZ:55636, HGNC:20626, HH5, IS3, KAL5, MIM:608892, NM_001316690, NM_017780, NP_001303619, NP_060250, XM_011517553, XM_011517554, XM_011517555, XM_011517560, XM_017013612, XM_017013613, XP_011515855, XP_011515856, XP_011515857, XP_011515862, XP_016869101, XP_016869102, chromodomain helicase DNA binding protein 7
Omim:OMIM:608892
Id:ENSG00000171316
Hgnc:HGNC:20626
Description:chromodomain helicase DNA binding protein 7
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]