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