cerebellum vermis hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the vermis (Mammalian Phenotype Ontology, MP_0000866)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000866
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9 gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CERS1 ceramide synthase 1
L1CAM L1 cell adhesion molecule
MKS1 Meckel syndrome, type 1
MSX2 msh homeobox 2
TMEM67 transmembrane protein 67
ZIC1 Zic family member 1
ZIC4 Zic family member 4
ZNF423 zinc finger protein 423