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XB-GENEPAGE-853844
kmt2b lysine methyltransferase 2B
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (20 sources): Abnormality of eye movement, Astigmatism, Bulbous nose, Cognitive impairment, Craniofacial dystonia, Dysarthria, Dysphonia, Dystonia, Gait disturbance, Global developmental delay, [+] |
Mouse (40 sources): abnormal brown fat cell differentiation, abnormal dentate gyrus morphology, abnormal fetal cardiomyocyte morphology, abnormal heart echocardiography feature, abnormal heart tube morphology, abnormal hippocampus granule cell layer, abnormal inner ear canal morphology, abnormal motor capabilities/coordination/movement, abnormal object recognition memory, abnormal pinna reflex, [+] |
View all ortholog results at Monarch |