Cerebellar Cortical Atrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Atrophy (wasting) of the cerebellar cortex. (Human Phenotype Ontology, HP_0008278)
External Link https://www.disgenet.org/browser/0/1/0/C4024710
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Genes

9 genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CAT catalase
MYO5A myosin VA (heavy chain 12, myoxin)
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PLAA phospholipase A2-activating protein
PPT1 palmitoyl-protein thioesterase 1
SC5D sterol-C5-desaturase
SHANK3 SH3 and multiple ankyrin repeat domains 3
SIL1 SIL1 nucleotide exchange factor
TPP1 tripeptidyl peptidase I