Inclusion body myositis Gene Set

Dataset	WikiPathways Pathways 2024
Category	structural or functional annotations
Type	pathway
Description	A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms. (Human Disease Ontology, DOID_3429)
External Link	https://www.wikipathways.org/pathways/WP5120.html
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Genes

11 proteins participating in the Inclusion body myositis pathway from the WikiPathways Pathways 2024 dataset.

Symbol	Name
APP	amyloid beta (A4) precursor protein
BACE1	beta-site APP-cleaving enzyme 1
MAPT	microtubule-associated protein tau
MSTN	myostatin
NCSTN	nicastrin
NFKB1	nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
NFKB2	nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PSEN1	presenilin 1
PSEN2	presenilin 2
PSENEN	presenilin enhancer gamma secretase subunit
SIRT1	sirtuin 1