Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol CHD7 contributors: mct - updated : 21-09-2015
HGNC name chromodomain helicase DNA binding protein 7
HGNC id 20626
ASSOCIATED DISORDERS
corresponding disease(s) CHARGE , DUP8Q12 , HHI5
Susceptibility to idiopathic scoliosis
Variant & Polymorphism SNP increasing the risk of idiopathic scoliosis
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • loss of Chd7 results in cell-autonomous proliferative, neurogenic and self-renewal defects in the perinatal and mature mouse subventricular zone (SVZ) stem cell niche