abnormal cerebellum anterior lobe morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the region of the cerebellum that is anterior to the primary fissure (Mammalian Phenotype Ontology, MP_0009960)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009960
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Genes

10 gene mutations causing the abnormal cerebellum anterior lobe 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
UNC5C unc-5 homolog C (C. elegans)
WNT1 wingless-type MMTV integration site family, member 1