grin2d Phenotypes

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.

Phenotypes

Gene Literature (48)

Nucleotides (60)

Interactants (23)

XB-GENEPAGE-1011862

Gene Symbol: grin2d Gene Name: 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, Abnormality of coordination, Abnormality of vision, Abnormal myelination, Absent speech, Ataxia, Attention deficit hyperactivity disorder, Atypical behavior, Autism, Axial hypotonia, Brain atrophy, Cerebral atrophy, Cerebral visual impairment, Decreased fetal movement, Delayed speech and language development, Developmental regression, Downslanted palpebral fissures, Dyskinesia, Dysphagia, EEG with multifocal slow activity, Encephalopathy, Epileptic encephalopathy, Failure to thrive, Feeding difficulties, Gastroesophageal reflux, Generalized hypotonia, Global developmental delay, High forehead, Hypodontia, Hyporeflexia, Hypsarrhythmia, Impulsivity, Intellectual disability, Involuntary movements, Limb hypertonia, Mental deterioration, Microcephaly, Myoclonus, Nystagmus, obsolete Difficulty walking, Optic atrophy, Pes planus, Poor head control, Ptosis, Reduced tendon reflexes, Retinal degeneration, Rigidity, Seizure, Short stature, Spasticity, Status epilepticus, Tremor, Unsteady gait [+]
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