Arthralgia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Joint pain. (Human Phenotype Ontology, HP_0002829)
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Genes

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

Symbol Name
COMT catechol-O-methyltransferase
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
HFE hemochromatosis
IL10 interleukin 10
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL2 interleukin 2
IL6 interleukin 6
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
LTA lymphotoxin alpha
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
PCSK6 proprotein convertase subtilisin/kexin type 6
TPMT thiopurine S-methyltransferase
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor