Gene: MYO7A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China. 21150918 2011
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China. 21150918 2011
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Phenotypes in defined genotypes including siblings with Usher syndrome. 21174530 2011
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Phenotypes in defined genotypes including siblings with Usher syndrome. 21174530 2011
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. 20132242 2010
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. 20132242 2010
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. 18181211 2008
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. 18181211 2008
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR MYO7A mutation screening in Usher syndrome type I patients from diverse origins. 17361009 2007
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR MYO7A mutation screening in Usher syndrome type I patients from diverse origins. 17361009 2007
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). 15221449 2004
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). 15221449 2004
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity. 10094549 1999
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity. 10094549 1999
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. 9171833 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins. 9382091 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. 9354784 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. 9171833 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. 9354784 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins. 9382091 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene. 8776602 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. 8900236 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. 8900236 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 GeneticVariation group CLINVAR A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene. 8776602 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.100 CausalMutation group CLINVAR Defective myosin VIIA gene responsible for Usher syndrome type 1B. 7870171 1995