Human Gene Set: KEGG_MEDICUS_VARIANT_MUTATION
      _INACTIVATED_P62_TO_PINK_PARKIN
      _MEDIATED_AUTOPHAGOSOME_FORMATION


Standard name KEGG_MEDICUS_VARIANT_MUTATION_INACTIVATED_P62_TO_PINK_PARKIN_MEDIATED_AUTOPHAGOSOME_FORMATION
Systematic name M47743
Brief description Pathway Definition from KEGG: PINK1 -> PRKN -> (CISD1,CISD2,FAF2,FKBP8,TOMM70,HK1) // SQSTM1* // LC3
Full description or abstract Mutation-inactivated p62 to PINK-Parkin-mediated autophagosome formation. Pathway ID: N01139. Pathway type: Variant. Pathway class: nt06464 Amyotrophic lateral sclerosis.
Collection C2: Curated
      CP: Canonical Pathways
            CP:KEGG_MEDICUS: KEGG Medicus Pathways
Source publication  
Exact source N01139
Related gene sets  
External links https://www.kegg.jp/entry/N01139
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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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Version history 2023.2.Hs: First Introduced.

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