×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
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
0.500
Biomarker
group
CLINGEN
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.
27583663
2016
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
CLINGEN
Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
25798947
2015
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
CLINGEN
Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.
24608321
2014
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
CLINGEN
Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
22381527
2012
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
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:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
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
0.500
Biomarker
group
CLINGEN
SANS (USH1G) expression in developing and mature mammalian retina.
17923142
2008
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
MGD
A quantitative survey of gravity receptor function in mutant mouse strains.
16235133
2005
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
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:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
CLINGEN
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
11941484
2002
×
Entrez Id:
124590
Gene Symbol:
USH1G
USH1G
0.500
Biomarker
group
MGD
Ultrastructural findings in the inner ear of Jackson shaker mice.
1442008
1992