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XB-GENEPAGE-987502
kctd7 potassium channel tetramerization domain containing 7
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (27 sources): Abnormality of vision, Aplasia/Hypoplasia of the corpus callosum, Bilateral tonic-clonic seizure, Cerebellar atrophy, Cerebral atrophy, Chin myoclonus, Dementia, Developmental regression, Dysarthria, EEG with focal epileptiform discharges, [+] |
Mouse (4 sources): abnormal hemoglobin content, decreased spleen weight, increased exploration in new environment, no abnormal phenotype detected |
View all ortholog results at Monarch |