Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
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
|
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
|
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
|
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
|
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
|
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 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
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
|
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
|
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
|
DEAFNESS, AUTOSOMAL RECESSIVE 2
|
0.930 |
Biomarker |
MGD |
Inner ear morphology is perturbed in two novel mouse models of recessive deafness.
|
23251483 |
2012 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
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
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
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
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
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
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
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
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
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
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker |
MGD |
Mutations in the myosin VIIa gene (MYO7A) cause a common and severe subtype of Usher syndrome (USH1B).Shaker1 mice have mutant MYO7A.
|
21447681 |
2011 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
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
|
Hereditary retinal dystrophy
|
0.500 |
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
|
Hereditary retinal dystrophy
|
0.500 |
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
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
|
14198707 |
1964 |