Gene: CHD7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome. 26670829 2015
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD "CHD7 deficiency in ""Looper"", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment." 24840056 2014
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene. 22539951 2012
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease CTD_human Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes. 21532573 2011
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 GeneticVariation disease BEFREE We observed somatic and germline mosaicism as well as parent-to-child transmission of non-mosaic CHD7 mutations as causes of familial CHARGE syndrome. 18074359 2008
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues. 17334657 2007
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome. 17701983 2007
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease CTD_human Phenotypic spectrum of CHARGE syndrome with CHD7 mutations. 16615981 2006
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.510 Biomarker disease MGD Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. 16207732 2005