KEGG Huntington disease - Homo sapiens (human)
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  • nt06410 Calcium signaling
    • N00985 Mutation-caused aberrant Htt to mGluR5-Ca2+ -apoptotic pathway
    • N00986 Mutation-caused aberrant Htt to VGCC-Ca2+ -apoptotic pathway
    • N00987 Mutation-caused aberrant Htt to transport of calcium
  • nt06420 Ubiquitin-proteasome system
    • N01061 Mutation-caused aberrant Htt to 26S proteasome-mediated protein degradation
  • nt06413 Autophagy
    • N00993 Mutation-caused aberrant Htt to autophagy-vesicle nucleation
  • nt06414 Apoptosis
    • N00983 Mutation-caused aberrant Htt to extrinsic apoptotic pathway
  • nt06416 TNF signaling
    • N00992 Mutation-caused aberrant Htt to TNF-JNK signaling pathway
  • nt06418 Oxidative phosphorylation
    • N00989 Mutation-caused aberrant Htt to electron transfer in Complex II
    • N00991 Mutation-caused aberrant Htt to electron transfer in Complex III
  • nt06419 Microtubule-based transport
    • N00977 Mutation-caused aberrant Htt to retrograde axonal transport
    • N00979 Mutation-caused aberrant Htt to anterograde axonal transport
  • nt06440 Transcription
    • N00980 Mutation-caused aberrant Htt to REST-mediated transcriptional repression
    • N00981 Mutation-caused aberrant Htt to CREB-mediated transcription
    • N00982 Mutation-caused aberrant Htt to p53-mediated transcription