fractures, bone Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Breaks in bones. (Experimental Factor Ontology, EFO_0003931)
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Genes

28 genes associated with the disease fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ARHGAP1 Rho GTPase activating protein 1
BGLAP bone gamma-carboxyglutamate (gla) protein
CER1 cerberus 1, DAN family BMP antagonist
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COMT catechol-O-methyltransferase
CRHR1 corticotropin releasing hormone receptor 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DCDC5 doublecortin domain containing 5
ESR1 estrogen receptor 1
F2 coagulation factor II (thrombin)
FOXL1 forkhead box L1
HDAC5 histone deacetylase 5
LRP4 low density lipoprotein receptor-related protein 4
LRP5 low density lipoprotein receptor-related protein 5
MEF2C myocyte enhancer factor 2C
MEPE matrix extracellular phosphoglycoprotein
SOX6 SRY (sex determining region Y)-box 6
SP7 Sp7 transcription factor
SPTBN1 spectrin, beta, non-erythrocytic 1
STARD3NL STARD3 N-terminal like
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
WLS wntless Wnt ligand secretion mediator
ZBTB40 zinc finger and BTB domain containing 40