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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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