|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A quantitative survey of gravity receptor function in mutant mouse strains.
|
16235133 |
2005 |
|
| Entrez Id: |
124590 |
| Gene Symbol: |
USH1G |
USH1G
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A quantitative survey of gravity receptor function in mutant mouse strains.
|
16235133 |
2005 |
|
| Entrez Id: |
65217 |
| Gene Symbol: |
PCDH15 |
PCDH15
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A quantitative survey of gravity receptor function in mutant mouse strains.
|
16235133 |
2005 |
|
| Entrez Id: |
124590 |
| Gene Symbol: |
USH1G |
USH1G
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
|
18339676 |
2008 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.
|
14609561 |
2003 |
|
| Entrez Id: |
25861 |
| Gene Symbol: |
WHRN |
WHRN
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss.
|
20502675 |
2010 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer.
|
9021139 |
1997 |
|
| 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: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
|
18339676 |
2008 |
|
| 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: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
|
11138008 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
CD1d1 mutant mice are deficient in natural T cells that promptly produce IL-4.
|
9133426 |
1997 |
|
| Entrez Id: |
10083 |
| Gene Symbol: |
USH1C |
USH1C
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
|
14519688 |
2003 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Cochlear histopathology of the mutant bustling mouse, BUS/Idr.
|
8790740 |
1996 |
|
| Entrez Id: |
10083 |
| Gene Symbol: |
USH1C |
USH1C
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Intestinal brush border assembly driven by protocadherin-based intermicrovillar adhesion.
|
24725409 |
2014 |
|
| Entrez Id: |
10083 |
| Gene Symbol: |
USH1C |
USH1C
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Ush1c216A knock-in mouse survives Katrina.
|
17174357 |
2007 |
|
| 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: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
|
11750125 |
2001 |
|
| Entrez Id: |
23568 |
| Gene Symbol: |
ARL2BP |
ARL2BP
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
ARL2BP, a protein linked to retinitis pigmentosa, is needed for normal photoreceptor cilia doublets and outer segment structure.
|
29718757 |
2018 |
|
| Entrez Id: |
65217 |
| Gene Symbol: |
PCDH15 |
PCDH15
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
|
18339676 |
2008 |
|
| Entrez Id: |
124590 |
| Gene Symbol: |
USH1G |
USH1G
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Ultrastructural findings in the inner ear of Jackson shaker mice.
|
1442008 |
1992 |
|
| 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 |
|
| Entrez Id: |
4647 |
| Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |