Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Myosin 7 and its adaptors link cadherins to actin. 28660889

2017

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Over-expression of myosin7A in cochlear hair cells of circling mice. 28400833

2017

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells. 27013738

2016

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing. 25211151

2014

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1. 23559863

2013

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN 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
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. 10958658

2000

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN In situ hybridization analysis in human embryos demonstrates that the myosin VIIA gene is expressed in the pigment epithelium and the photoreceptor cells of the retina, thus indicating that both cell types may be involved in the USH1B retinal degenerative process. 8622919

1996

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
0.700 Biomarker CLINGEN A type VII myosin encoded by the mouse deafness gene shaker-1. 7870172

1995