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XB-GENEPAGE-998875
mfsd8 major facilitator superfamily domain containing 8
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (21 sources): Ataxia, Blindness, Bull's eye maculopathy, Central scotoma, Cerebellar atrophy, Cerebral atrophy, Delayed speech and language development, EEG abnormality, Generalized myoclonic seizure, Global developmental delay, [+] |
Mouse (8 sources): CNS inflammation, abnormal kidney morphology, abnormal lysosome morphology, abnormal myocardial fiber morphology, abnormal retina vasculature morphology, decreased hemoglobin content, microgliosis, retina photoreceptor degeneration |
View all ortholog results at Monarch |