abnormal cerebellum anterior vermis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior portion of the narrow middle zone between the two hemispheres of the cerebellum that is located anterior to the primary fissure (Mammalian Phenotype Ontology, MP_0000867)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000867
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Genes

9 gene mutations causing the abnormal cerebellum anterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EBF2 early B-cell factor 2
EN1 engrailed homeobox 1
FGF17 fibroblast growth factor 17
FOXB1 forkhead box B1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MID1 midline 1
MSX2 msh homeobox 2
NPC1 Niemann-Pick disease, type C1
WNT1 wingless-type MMTV integration site family, member 1