Fractures, Bone Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Breaks in bones. (Experimental Factor Ontology, EFO_0003931)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D050723
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Genes

10 genes/proteins associated with the disease Fractures, Bone from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DKK1 dickkopf WNT signaling pathway inhibitor 1 2.88009
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B 2.88009
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13 2.88009
FAM210A family with sequence similarity 210, member A 2.88009
TGFBR2 transforming growth factor, beta receptor II (70/80kDa) 2.88009
IRX5 iroquois homeobox 5 2.88009
SPTBN1 spectrin, beta, non-erythrocytic 1 2.88009
LRP5 low density lipoprotein receptor-related protein 5 2.88009
MEPE matrix extracellular phosphoglycoprotein 2.88009
PTH parathyroid hormone 2.88009