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XB-GENEPAGE-946115
coq8a coenzyme Q8A
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (31 sources): Abnormal pyramidal sign, Ataxia, Brisk reflexes, Cerebellar atrophy, Developmental regression, Dystonia, EMG abnormality, Exercise intolerance, Focal T2 hypointense basal ganglia lesion, Generalized hypotonia, [+] |
Mouse (9 sources): Purkinje cell degeneration, abnormal Purkinje cell morphology, abnormal enzyme/coenzyme level, abnormal skeletal muscle morphology, abnormal spatial reference memory, environmentally induced seizures, impaired exercise endurance, increased susceptibility to pharmacologically induced seizures, skeletal muscle fiber degeneration |
View all ortholog results at Monarch |