Rhabdomyolysis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Breakdown of muscle fibers that leads to the release of muscle fiber contents (myoglobin) into the bloodstream. (Human Phenotype Ontology, HP_0003201)
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Genes

20 genes associated with the Rhabdomyolysis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACTN3 actinin, alpha 3 (gene/pseudogene)
AMPD1 adenosine monophosphate deaminase 1
CCL2 chemokine (C-C motif) ligand 2
CCR2 chemokine (C-C motif) receptor 2
CKM creatine kinase, muscle
CYP2C18 cytochrome P450, family 2, subfamily C, polypeptide 18
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HBB hemoglobin, beta
HSPA1B heat shock 70kDa protein 1B
IL6 interleukin 6
LPIN1 lipin 1
LPIN2 lipin 2
LPIN3 lipin 3
MYLK myosin light chain kinase
MYLK2 myosin light chain kinase 2
SLCO1B1 solute carrier organic anion transporter family, member 1B1
TNF tumor necrosis factor
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1