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 		1.000 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease MGD The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations. 6627025 1983
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease BEFREE Of three different genes responsible for USH1.USH1B maps to 11q13.5 (ref. 7870171 1995
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease UNIPROT Of three different genes responsible for USH1.USH1B maps to 11q13.5 (ref. 7870171 1995
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease GENOMICS_ENGLAND Of three different genes responsible for USH1.USH1B maps to 11q13.5 (ref. 7870171 1995
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease CLINGEN A type VII myosin encoded by the mouse deafness gene shaker-1. 7870172 1995
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease CLINGEN Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia. 8622919 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease BEFREE Usher syndrome type I (US1) is an autosomal recessive condition in which three different genes have been already localised (USH1A, USH1B, and USH1C on chromosomes 14q32, 11q13, and 11p15 respectively). 8825055 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease UNIPROT Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. 8900236 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease BEFREE Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. 8900236 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease CLINVAR Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. 8900236 1996
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease BEFREE Four loci responsible for USH1 (USH1A, 1B, 1C and 1D) have previously been mapped, among which only the USH1B gene has been cloned. 9002666 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease CLINVAR Primers covering the complete myosin VIIA coding sequence as well as the 3' non coding sequence were designed, allowing direct sequence analysis of each of the 48 coding exons and flanking splice sites in seven patients affected by USH1. 9002678 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease BEFREE Primers covering the complete myosin VIIA coding sequence as well as the 3' non coding sequence were designed, allowing direct sequence analysis of each of the 48 coding exons and flanking splice sites in seven patients affected by USH1. 9002678 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease UNIPROT Primers covering the complete myosin VIIA coding sequence as well as the 3' non coding sequence were designed, allowing direct sequence analysis of each of the 48 coding exons and flanking splice sites in seven patients affected by USH1. 9002678 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 CausalMutation disease CLINVAR Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. 9171832 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 CausalMutation disease 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 		1.000 GeneticVariation disease 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 		1.000 GeneticVariation disease UNIPROT 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 		1.000 Biomarker disease MGD Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. 9435277 1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease BEFREE With regard to Usher type I (USH1), several subtypes have been described, the most frequent being USH1B located on chromosome 11q13.5. 9610802 1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294 1997
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 CausalMutation disease CLINVAR Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome. 9718356 1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 GeneticVariation disease UNIPROT Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome. 9718356 1998
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		1.000 Biomarker disease GENOMICS_ENGLAND Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib. 9843659 1998