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Summary Expression Phenotypes Gene Literature (8) GO Terms (3) Nucleotides (67) Proteins (40) Interactants (130) Wiki
XB-GENEPAGE-1013606

ush1g     Usher syndrome 1G (autosomal recessive)

Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal cochlea morphology, Abnormal dental enamel morphology, Abnormal electroretinogram, Absent vestibular function, Anxiety, Aplasia/Hypoplasia of the cerebellum, Ataxia, Cataract, Cerebral cortical atrophy, Depression, [+]
Mouse (34 sources): abnormal cochlear hair bundle tip links morphology, abnormal cochlear hair cell inter-stereocilial links morphology, abnormal hair cell mechanoelectric transduction, abnormal hair cell physiology, abnormal hearing electrophysiology, abnormal inner hair cell stereociliary bundle morphology, abnormal orientation of cochlear hair cell stereociliary bundles, abnormal outer hair cell kinocilium location or orientation, abnormal outer hair cell stereociliary bundle morphology, abnormal pinna reflex, [+]

View all ortholog results at Monarch