kcnc3 Phenotypes

Phenotypes

XB-GENEPAGE-958407

Gene Symbol: kcnc3 Gene Name: potassium channel, voltage gated Shaw related subfamily C, member 3

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (38 sources): Abnormal facial shape, Abnormal pyramidal sign, Abnormal pyramidal tract morphology, Bradykinesia, Cerebellar atrophy, Clumsiness, Difficulty running, Dysarthria, Dysphagia, Gait ataxia, Generalized hypotonia, Global developmental delay, Hearing impairment, Hyperactive deep tendon reflexes, Hyperreflexia, Hypotonia, Impaired distal vibration sensation, Impaired visuospatial constructive cognition, Intellectual disability, Intellectual disability, mild, Jerky ocular pursuit movements, Limb ataxia, Limb dysmetria, Motor delay, Myoclonus, Nystagmus, obsolete Difficulty walking, Optic atrophy, Optic disc pallor, Postural instability, Progressive cerebellar ataxia, Seizure, Short stature, Titubation, Torticollis, Upgaze palsy, Urinary incontinence, Urinary urgency [+]
Mouse (9 sources): abnormal body length, abnormal grip strength, abnormal locomotor activation, abnormal locomotor behavior, decreased bone mineral content, decreased grip strength, increased grip strength, increased vertical activity, no abnormal phenotype detected
View all ortholog results at Monarch