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XB-GENEPAGE-954770
rnf13 ring finger protein 13
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (20 sources): Cataract, Cerebral visual impairment, Delayed myelination, Delayed skeletal maturation, Epileptic encephalopathy, Failure to thrive, Flexion contracture, Generalized hypotonia, Hip dysplasia, Hypoplasia of the corpus callosum, [+] |
Mouse (5 sources): abnormal heart rate, abnormal hindlimb morphology, abnormal limb position, abnormal sleep behavior, abnormal urine creatinine level |
View all ortholog results at Monarch |