kcna2 Phenotypes

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Phenotypes

Gene Literature (117)

Nucleotides (52)

Interactants (118)

XB-GENEPAGE-991583

Gene Symbol: kcna2 Gene Name: potassium channel, voltage gated shaker related subfamily A, member 2

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (51 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, Brain atrophy, Cerebral atrophy, Cleft palate, Decreased fetal movement, Delayed speech and language development, Developmental regression, Difficulty walking, Downslanted palpebral fissures, Dyskinesia, 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, Poor head control, Ptosis, Reduced tendon reflexes, Retinal degeneration, Rigidity, Seizure, Short stature, Spasticity, Status epilepticus, Tremor, Unsteady gait [+]
Mouse (19 sources): abnormal action potential, abnormal brain wave pattern, abnormal channel response, abnormal inhibitory postsynaptic currents, abnormal miniature inhibitory postsynaptic currents, abnormal single cell response, abnormal sleep pattern, behavior/neurological phenotype, decreased body size, decreased grip strength, impaired ability to fire action potentials, increased susceptibility to pharmacologically induced seizures, limb grasping, long stride length, nervous system phenotype, postnatal lethality, postnatal lethality, complete penetrance, premature death, tonic seizures [+]
View all ortholog results at Monarch