bone remodeling disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A bone disease that results_in formation or resorption abnormalities located_in bone. (Human Disease Ontology, DOID_0080005)
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Genes

22 genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
CA2 carbonic anhydrase II
CLCN7 chloride channel, voltage-sensitive 7
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
EXT1 exostosin glycosyltransferase 1
EXT2 exostosin glycosyltransferase 2
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LRP5 low density lipoprotein receptor-related protein 5
MIR4315-1 microRNA 4315-1
MIR4315-2 microRNA 4315-2
OSTM1 osteopetrosis associated transmembrane protein 1
SNX10 sorting nexin 10
SOST sclerostin
SQSTM1 sequestosome 1
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TGFB1 transforming growth factor, beta 1
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
TRPS1 trichorhinophalangeal syndrome I
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor