×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
USHER SYNDROME, TYPE IA, FORMERLY
0.500
Biomarker
CLINGEN
Myosin 7 and its adaptors link cadherins to actin.
28660889
2017
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
USHER SYNDROME, TYPE IA, FORMERLY
0.500
Biomarker
CLINGEN
Over-expression of myosin7A in cochlear hair cells of circling mice.
28400833
2017
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
USHER SYNDROME, TYPE IA, FORMERLY
0.500
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
USHER SYNDROME, TYPE IA, FORMERLY
0.500
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
USHER SYNDROME, TYPE IA, FORMERLY
0.500
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
USHER SYNDROME, TYPE IA, FORMERLY
0.500
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
USHER SYNDROME, TYPE IA, FORMERLY
0.500
Biomarker
CLINGEN
Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.
10958658
2000
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
USHER SYNDROME, TYPE IA, FORMERLY
0.500
Biomarker
CLINGEN
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.
8622919
1996
×
Entrez Id:
4647
Gene Symbol:
MYO7A
MYO7A
USHER SYNDROME, TYPE IA, FORMERLY
0.500
Biomarker
CLINGEN
A type VII myosin encoded by the mouse deafness gene shaker-1.
7870172
1995
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.
27583663
2016
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
26936824
2016
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
25798947
2015
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.
24608321
2014
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
22381527
2012
×
Entrez Id:
64072
Gene Symbol:
CDH23
CDH23
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
21689626
2011
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.
21436032
2011
×
Entrez Id:
64072
Gene Symbol:
CDH23
CDH23
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Nasal epithelial cells are a reliable source to study splicing variants in Usher syndrome.
20513143
2010
×
Entrez Id:
10083
Gene Symbol:
USH1C
USH1C
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Novel mutations in the USH1C gene in Usher syndrome patients.
21203349
2010
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
SANS (USH1G) expression in developing and mature mammalian retina.
17923142
2008
×
Entrez Id:
65217
Gene Symbol:
PCDH15
PCDH15
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli.
16260500
2005
×
Entrez Id:
65217
Gene Symbol:
PCDH15
PCDH15
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Duplicated genes with split functions: independent roles of protocadherin15 orthologues in zebrafish hearing and vision.
15634702
2005
×
Entrez Id:
65217
Gene Symbol:
PCDH15
PCDH15
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).
15928608
2005
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
12588794
2003
×
Entrez Id:
65217
Gene Symbol:
PCDH15
PCDH15
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.
12782354
2003
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
USHER SYNDROME, TYPE IA, FORMERLY
0.300
Biomarker
CLINGEN
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
11941484
2002