absent cerebellum fissure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009268
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1 gene mutations causing the absent cerebellum fissure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6