grin2d Phenotypes

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Phenotypes

Gene Literature (47)

Nucleotides (60)

Interactants (21)

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, Abnormal myelination, Abnormality of coordination, Abnormality of vision, Absent speech, Ataxia, Attention deficit hyperactivity disorder, Autism, Axial hypotonia, Behavioral abnormality, Brain atrophy, Cerebral atrophy, Cerebral visual impairment, Decreased fetal movement, Delayed speech and language development, Developmental regression, Difficulty walking, 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, 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