abnormal purkinje cell differentiation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical production of or inability to produce the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex (Mammalian Phenotype Ontology, MP_0008579)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008579
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5 gene mutations causing the abnormal purkinje cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
GPR37L1 G protein-coupled receptor 37 like 1
NR1D1 nuclear receptor subfamily 1, group D, member 1
RORA RAR-related orphan receptor A
SKOR2 SKI family transcriptional corepressor 2