kcnn2 Phenotypes

Phenotypes

XB-GENEPAGE-6077410

Gene Symbol: kcnn2 Gene Name: potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: kcnn2 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (32 sources): abnormal CNS synaptic transmission, abnormal action potential, abnormal afterhyperpolarization, abnormal brain white matter morphology, abnormal coat appearance, abnormal contextual conditioning behavior, abnormal cued conditioning behavior, abnormal excitatory postsynaptic potential, abnormal involuntary movement, abnormal locomotor behavior, abnormal locomotor coordination, abnormal sexual interaction, abnormal short term object recognition memory, abnormal single cell response, abnormal spatial learning, abnormal spinal cord white matter morphology, decreased body size, decreased physiological sensitivity to xenobiotic, decreased vertical activity, hearing/vestibular/ear phenotype, hunched posture, impaired limb coordination, no abnormal phenotype detected, postnatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, prenatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, reduced long term potentiation, reduced male fertility, reproductive system phenotype, short stride length, vision/eye phenotype [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (32 sources): abnormal CNS synaptic transmission, abnormal action potential, abnormal afterhyperpolarization, abnormal brain white matter morphology, abnormal coat appearance, abnormal contextual conditioning behavior, abnormal cued conditioning behavior, abnormal excitatory postsynaptic potential, abnormal involuntary movement, abnormal locomotor behavior, [+]