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
|
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
|
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
|
USHER SYNDROME, TYPE IA, FORMERLY
|
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
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
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
|
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 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
|
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
|
USHER SYNDROME, TYPE IA, FORMERLY
|
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
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
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
|
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 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
|
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
|
USHER SYNDROME, TYPE IA, FORMERLY
|
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
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
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
|
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 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
|
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 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
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, FRENCH VARIETY, FORMERLY
|
0.500 |
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
|
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
|
Sensorineural hearing loss, bilateral
|
0.300 |
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 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
|
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
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
Moderate light-induced degeneration of rod photoreceptors with delayed transducin translocation in shaker1 mice.
|
21447681 |
2011 |