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XB-GENEPAGE-990004
rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (16 sources): Ataxia, Cerebellar atrophy, Delayed gross motor development, Delayed speech and language development, Dysarthria, Gait ataxia, Hyperreflexia, Hyporeflexia, Intellectual disability, Limb ataxia, [+] |
View all ortholog results at Monarch |