Human Gene Set: KEGG_MEDICUS_VARIANT_MUTATION_CAUSED
      _ABERRANT_ABETA_TO_VGCC_CA2_APOPTOTIC
      _PATHWAY_N01006


Standard name KEGG_MEDICUS_VARIANT_MUTATION_CAUSED_ABERRANT_ABETA_TO_VGCC_CA2_APOPTOTIC_PATHWAY_N01006
Systematic name M47693
Brief description Pathway Definition from KEGG: APP* -> Abeta -> PPID -> MPTP -> CYCS
Full description or abstract Mutation-caused aberrant Abeta to VGCC-Ca2+ -apoptotic pathway. Pathway ID: N01006. Pathway type: Variant. Pathway class: nt06460 Alzheimer disease.
Collection C2: Curated
      CP: Canonical Pathways
            CP:KEGG_MEDICUS: KEGG Medicus Pathways
Source publication  
Exact source N01006
Related gene sets  
External links https://www.kegg.jp/entry/N01006
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Source species Homo sapiens
Contributed by KEGG (Kyoto Encyclopedia of Genes and Genomes)
Source platform or
identifier namespace
Human_NCBI_Gene_ID
Dataset references  
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NCI-60 cell lines (National Cancer Institute)
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Version history 2023.2.Hs: First Introduced.

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