|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows (Mammalian Phenotype Ontology, MP_0009268)|
|Downloads & Tools|
1 gene mutations causing the absent cerebellum fissure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|KCNJ6||potassium channel, inwardly rectifying subfamily J, member 6|