abnormal cerebellar lobule formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the lobes of the cerebellum (Mammalian Phenotype Ontology, MP_0006097)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006097
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Genes

10 gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B4GALT2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2
CTNNA2 catenin (cadherin-associated protein), alpha 2
EN1 engrailed homeobox 1
FIGN fidgetin
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
MID1 midline 1
NEUROD4 neuronal differentiation 4
PAX5 paired box 5
SKOR2 SKI family transcriptional corepressor 2
UNC5C unc-5 homolog C (C. elegans)