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XB-GENEPAGE-1011862
grin2d glutamate receptor, ionotropic, N-methyl D-aspartate 2D
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (54 sources): Abnormal corpus callosum morphology, Abnormal involuntary eye movements, Abnormal myelination, Abnormality of coordination, Abnormality of vision, Absent speech, Ataxia, Attention deficit hyperactivity disorder, Autism, Axial hypotonia, [+] |
Mouse (9 sources): abnormal bone mineralization, behavior/neurological phenotype, decreased heart weight, decreased lean body mass, decreased locomotor activity, decreased vertical activity, increased bone mineral content, increased startle reflex, nervous system phenotype |
View all ortholog results at Monarch |