absent cerebellum Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	missing the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement (Mammalian Phenotype Ontology, MP_0000850)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000850
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Genes

11 gene mutations causing the absent cerebellum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
EN1	engrailed homeobox 1
FGF8	fibroblast growth factor 8 (androgen-induced)
GBX2	gastrulation brain homeobox 2
LMX1B	LIM homeobox transcription factor 1, beta
PAX2	paired box 2
PHGDH	phosphoglycerate dehydrogenase
PTF1A	pancreas specific transcription factor, 1a
SP8	Sp8 transcription factor
WNT1	wingless-type MMTV integration site family, member 1
ZIC3	Zic family member 3
ZNF423	zinc finger protein 423