Human Gene Set: KEGG_MEDICUS_VARIANT_MUTATION_INACTIVATED_PRKN_TO_MGLUR1_SIGNALING_PATHWAY


Standard name KEGG_MEDICUS_VARIANT_MUTATION_INACTIVATED_PRKN_TO_MGLUR1_SIGNALING_PATHWAY
Systematic name M49000
Brief description Pathway Definition from KEGG: PRKN* -> PLCG1 -> IP3 -> ITPR -> Ca2+
Full description or abstract Mutation-inactivated PRKN to mGluR1 signaling pathway. Pathway ID: N01032. Pathway type: Variant. Pathway class: nt06463 Parkinson disease.
Collection C2: Curated
      CP: Canonical Pathways
            CP:KEGG_MEDICUS: KEGG Medicus Pathways
Source publication  
Exact source N01032
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External links https://www.kegg.jp/entry/N01032
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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
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Version history 2024.1.Hs: Updated to network file downloaded on 2024-05-334

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