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XB-GENEPAGE-990891
rdx radixin
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (1 source): Profound sensorineural hearing impairment |
Mouse (16 sources): abnormal blood homeostasis, abnormal cochlear hair cell stereociliary bundle morphology, abnormal inner hair cell stereociliary bundle morphology, abnormal outer hair cell stereociliary bundle morphology, absent pinna reflex, cochlear hair cell degeneration, deafness, fused inner hair cell stereocilia, fused outer hair cell stereocilia, increased circulating alkaline phosphatase level, [+] |
View all ortholog results at Monarch |