rhabdomyolysis Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. (Experimental Factor Ontology, EFO_0003867)
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Genes

14 genes co-occuring with the biological term rhabdomyolysis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ACADVL acyl-CoA dehydrogenase, very long chain
CKM creatine kinase, muscle
COX3
CPT1B carnitine palmitoyltransferase 1B (muscle)
CPT2 carnitine palmitoyltransferase 2
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
LDHA lactate dehydrogenase A
LPIN1 lipin 1
LPIN2 lipin 2
LPIN3 lipin 3
MB myoglobin
RYR1 ryanodine receptor 1 (skeletal)