absent cerebellum vermis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing narrow middle zone between the two hemispheres of the cerebellum (Mammalian Phenotype Ontology, MP_0000865)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000865
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3 gene mutations causing the absent cerebellum vermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ERBB3 erb-b2 receptor tyrosine kinase 3
TP53 tumor protein p53
ZNF423 zinc finger protein 423