Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (48) GO Terms (0) Nucleotides (51) Proteins (30) Interactants (20) Wiki

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.
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, Behavioral abnormality, [+]
Mouse (9 sources): abnormal bone mineralization, behavior/neurological phenotype, decreased heart weight, decreased lean body mass, decreased vertical activity, hypoactivity, increased bone mineral content, increased startle reflex, nervous system phenotype

View all ortholog results at Monarch