Human Gene Set: KEGG_MEDICUS_VARIANT_MUTATION_CAUSED
      _ABERRANT_SOD1_TO_RETROGRADE_AXONAL
      _TRANSPORT


Standard name KEGG_MEDICUS_VARIANT_MUTATION_CAUSED_ABERRANT_SOD1_TO_RETROGRADE_AXONAL_TRANSPORT
Systematic name M47754
Brief description Pathway Definition from KEGG: SOD1* -| (DCTN+DNAH+DNAI+DNALI1+DNAL)
Full description or abstract Mutation-caused aberrant SOD1 to retrograde axonal transport. Pathway ID: N01160. 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 N01160
Related gene sets  
External links https://www.kegg.jp/entry/N01160
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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)
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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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