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XB-GENEPAGE-973174
ufm1 ubiquitin-fold modifier 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (30 sources): Absent speech, Ataxia, Axial hypotonia, Blindness, Cerebellar atrophy, Cerebral atrophy, Cerebral hypomyelination, Choreoathetosis, Delayed speech and language development, Dysarthria, [+] |
Mouse (12 sources): abnormal brain development, decreased bone mineral content, decreased hemoglobin content, decreased lean body mass, decreased midbrain size, decreased neocortex size, decreased red blood cell distribution width, increased brain apoptosis, increased neuron apoptosis, increased total body fat amount, [+] |
View all ortholog results at Monarch |