KEGG Spinocerebellar ataxia - Homo sapiens (human)
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  • nt06410 Calcium signaling
    • N00960 Mutation-caused aberrant SPTBN2 to mGluR1-TRPC3 signaling pathway
    • N00954 Mutation-activated GRM1 to mGluR1-TRPC3 signaling pathway
    • N00958 Mutation-activated ITPR1 to mGluR1-TRPC3 signaling pathway
    • N00959 ITPR1-reduced expression to mGluR1-TRPC3 signaling pathway
    • N00955 Mutation-inactivated PRKCG to mGluR1-TRPC3 signaling pathway
    • N00956 Mutation-activated PRKCG to mGluR1-TRPC3 signaling pathway
    • N00961 Mutation-activated TRPC3 to mGluR1-TRPC3 signaling pathway
    • N00957 Mutation-caused abberant ATXN2/3 to mGluR5-Ca2+ -apoptotic pathway
    • N00968 Mutation-activated CACNA1A to VGCC-Ca2+ -apoptotic pathway
    • N00969 Mutation-inactivated CACNA1A to VGCC-Ca2- -apoptotic pathway
    • N00971 Mutation-caused aberrant PDYN to transport of calcium
  • nt06411 Potassium transport
    • N00973 Mutation-inactivated KCNC3 to transport of potassium
    • N00975 Mutation-inactivated KCND3 to transport of potassium
  • nt06413 Autophagy
    • N00962 Mutation-inactivated ATXN3 to autophagy-vesicle nucleation
  • nt06415 PI3K signaling
    • N00964 DAB1-overexpression to RELN-VLDLR-PI3K signaling pathway
  • nt06440 Transcription
    • N00966 Mutation-caused aberrant ATXN1 to RORA-mediated transcription