Cerebellar Function Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0742034
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Genes

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

Symbol Name
ANO2 anoctamin 2, calcium activated chloride channel
ATXN7 ataxin 7
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CAMTA1 calmodulin binding transcription activator 1
CSTB cystatin B (stefin B)
DMD dystrophin
GRM1 glutamate receptor, metabotropic 1
KCNK3 potassium channel, two pore domain subfamily K, member 3
MGLL monoglyceride lipase
NOVA2 neuro-oncological ventral antigen 2
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SOX2 SRY (sex determining region Y)-box 2
TRPV3 transient receptor potential cation channel, subfamily V, member 3
UBE3A ubiquitin protein ligase E3A