XB-GENEPAGE-989510
kcnq5 potassium channel, voltage gated KQT-like subfamily Q, member 5
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.
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| Computed annotations: kcnq5 assayed (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (9 sources): Abnormality of refraction, Absent speech, Epileptic encephalopathy, Generalized hypotonia, Global developmental delay, Intellectual disability, Myopia, Seizure, Unsteady gait |
| Mouse (2 sources): abnormal afterhyperpolarization, prenatal lethality, incomplete penetrance |
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View all ortholog results at Monarch |