Temporomandibular Joint Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

30 genes associated with the Temporomandibular Joint Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE2 angiotensin I converting enzyme 2
ADRB2 adrenoceptor beta 2, surface
ANKH ANKH inorganic pyrophosphate transport regulator
APP amyloid beta (A4) precursor protein
CAMK4 calcium/calmodulin-dependent protein kinase IV
CCL2 chemokine (C-C motif) ligand 2
CHRM2 cholinergic receptor, muscarinic 2
COMT catechol-O-methyltransferase
CXCL8 chemokine (C-X-C motif) ligand 8
DRD4 dopamine receptor D4
ESR1 estrogen receptor 1
GRK5 G protein-coupled receptor kinase 5
GSTM1 glutathione S-transferase mu 1
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-C major histocompatibility complex, class I, C
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
IFRD1 interferon-related developmental regulator 1
IL1RN interleukin 1 receptor antagonist
MMP1 matrix metallopeptidase 1
MMP3 matrix metallopeptidase 3
MMP9 matrix metallopeptidase 9
MPDZ multiple PDZ domain protein
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
SCN1A sodium channel, voltage gated, type I alpha subunit
TGFB1 transforming growth factor, beta 1
TPH1 tryptophan hydroxylase 1
TXNRD2 thioredoxin reductase 2