Bone Resorption Gene Set

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

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

Symbol Name
ACTN3 actinin, alpha 3 (gene/pseudogene)
ALAD aminolevulinate dehydratase
APOB apolipoprotein B
APOE apolipoprotein E
CIITA class II, major histocompatibility complex, transactivator
CLEC10A C-type lectin domain family 10, member A
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
ESR1 estrogen receptor 1
FDPS farnesyl diphosphate synthase
HSPA1L heat shock 70kDa protein 1-like
HSPA2 heat shock 70kDa protein 2
IFNG interferon, gamma
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1R1 interleukin 1 receptor, type I
IL6 interleukin 6
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOD1 nucleotide-binding oligomerization domain containing 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PTH1R parathyroid hormone 1 receptor
TAS1R3 taste receptor, type 1, member 3
TNF tumor necrosis factor
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor