Congenital Cerebellar Ataxia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0852975
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Genes

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

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
GRID2 glutamate receptor, ionotropic, delta 2
GRM1 glutamate receptor, metabotropic 1
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
SPTBN2 spectrin, beta, non-erythrocytic 2
THG1L tRNA-histidine guanylyltransferase 1-like (S. cerevisiae)
ZNF592 zinc finger protein 592