×
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