Usher Syndromes Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

14 genes associated with the Usher Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
ADGRV1 adhesion G protein-coupled receptor V1
CDH23 cadherin-related 23
CDHR1 cadherin-related family member 1
CLRN1 clarin 1
DFNB31 deafness, autosomal recessive 31
EYS eyes shut homolog (Drosophila)
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
MYO7A myosin VIIA
RHO rhodopsin
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH1G Usher syndrome 1G (autosomal recessive)
USH2A Usher syndrome 2A (autosomal recessive, mild)