Bone Diseases Gene Set

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

23 genes associated with the Bone Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADRB2 adrenoceptor beta 2, surface
AQP9 aquaporin 9
BMP4 bone morphogenetic protein 4
COL1A1 collagen, type I, alpha 1
CTR9 CTR9, Paf1/RNA polymerase II complex component
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
ESR1 estrogen receptor 1
GSK3B glycogen synthase kinase 3 beta
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF1R insulin-like growth factor 1 receptor
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
NMU neuromedin U
POR P450 (cytochrome) oxidoreductase
RUNX2 runt-related transcription factor 2
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TPH1 tryptophan hydroxylase 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor