Pathway
Inclusion body myositis
Inclusion body myositis (IBM) is a rare muscle degeneration diseases. It is caused by presumably both genetic risk factors and environmental factors stimulated by increasing age. The mechanism of p...
WP:5120
What the reference databases state
Statements
11 statements
11 statements · 1 reference database · Subject: Inclusion body myositis · Sources: WikiPathways
- APP participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- BACE1 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- MAPT participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- MSTN participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- NCSTN participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- NFKB1 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- NFKB2 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- PSEN1 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- PSEN2 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- PSENEN participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only
- SIRT1 participates in Inclusion body myositisProteinWikiPathways WP5120Inferred only