abnormal cerebellum fissure morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows (Mammalian Phenotype Ontology, MP_0009267)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009267
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6 gene mutations causing the abnormal cerebellum fissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CADPS2 Ca++-dependent secretion activator 2
EDARADD EDAR-associated death domain
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
LRP2 low density lipoprotein receptor-related protein 2
MID1 midline 1
PDS5A PDS5 cohesin associated factor A