myositis Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	An inflammatory process affecting the skeletal muscles. Causes include infections, injuries, and autoimmune disorders.\|Inflammation of a muscle or muscle tissue. (Experimental Factor Ontology, EFO_0000783)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004510
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Genes

17 gene mutations causing the myositis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
APP	amyloid beta (A4) precursor protein
CEBPB	CCAAT/enhancer binding protein (C/EBP), beta
COL13A1	collagen, type XIII, alpha 1
ITGB3	integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LAMA2	laminin, alpha 2
LARGE	like-glycosyltransferase
MYH4	myosin, heavy chain 4, skeletal muscle
PAX7	paired box 7
RELA	v-rel avian reticuloendotheliosis viral oncogene homolog A
RELB	v-rel avian reticuloendotheliosis viral oncogene homolog B
SGCB	sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SH3BP2	SH3-domain binding protein 2
SOCS1	suppressor of cytokine signaling 1
SYT7	synaptotagmin VII
TGFB1	transforming growth factor, beta 1
TREX1	three prime repair exonuclease 1
TTN	titin