Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD Moderate light-induced degeneration of rod photoreceptors with delayed transducin translocation in shaker1 mice. 21447681

2011

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells. 20016096

2009

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. 17329413

2007

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. 15389316

2004

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker 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
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD Mutation analysis of the mouse myosin VIIA deafness gene. 9680294

1997

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker 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
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. 14198707

1964

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
1.000 Biomarker MGD The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. 13336002

1956