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.

Summary Expression Phenotypes Gene Literature (91) GO Terms (0) Nucleotides (103) Proteins (39) Interactants (133) Wiki
XB-GENEPAGE-6047372

kcnq2     potassium channel, voltage gated KQT-like subfamily Q, 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: kcnq2 assayed (5 sources)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (46 sources): Abnormal cerebral white matter morphology, Abnormal globus pallidus morphology, Abnormality of movement, Abnormality of the orbital region, Abnormality of vision, Apnea, Bilateral tonic-clonic seizure, Cerebral atrophy, Cerebral edema, Choreoathetosis, [+]
Mouse (24 sources): abnormal action potential, abnormal afterhyperpolarization, abnormal brain wave pattern, abnormal neuron physiology, abnormal primary motor cortex morphology, abnormal seizure response to electrical stimulation, abnormal somatosensory cortex morphology, behavior/neurological phenotype, clonic seizures, decreased body size, [+]

View all ortholog results at Monarch