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XB-GENEPAGE-971527
slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (32 sources): Absent speech, Babinski sign, CNS hypomyelination, Cataract, Cerebellar atrophy, Cerebral atrophy, Clonus, Decreased circulating ceruloplasmin concentration, Degeneration of the lateral corticospinal tracts, Developmental cataract, [+] |
Mouse (27 sources): abnormal T cell activation, abnormal autophagy, abnormal circulating cytokine level, abnormal motor capabilities/coordination/movement, abnormal spinal cord white matter morphology, decreased corpus callosum size, decreased grip strength, decreased survivor rate, dermatitis, embryonic growth arrest, [+] |
View all ortholog results at Monarch |