paget's disease of bone Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A bone formation disease that has_material_basis_in hyperactive osteoclast which results_in abnormal osteoblast bone formation located_in skull, located_in pelvis, located_in vertebral column, located_in set of limbs. (Human Disease Ontology, DOID_5408)
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21 genes associated with the disease paget's disease of bone in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
OPTN optineurin 1.96161
PML promyelocytic leukemia 1.00628
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator 0.916033
RIN3 Ras and Rab interactor 3 0.774217
NUP205 nucleoporin 205kDa 0.641775
SLC25A43 solute carrier family 25, member 43 0.403461
CXCR4 chemokine (C-X-C motif) receptor 4 0.256228
UBXN4 UBX domain protein 4 0.197766
PIGN phosphatidylinositol glycan anchor biosynthesis, class N 0.15771
TBC1D5 TBC1 domain family, member 5 0.15771
PRL prolactin 0.126165
R3HDM1 R3H domain containing 1 0.100789
SHISA9 shisa family member 9 0.100789
ZRANB3 zinc finger, RAN-binding domain containing 3 0.100789
LCT lactase 0.100789
KIAA1468 KIAA1468 0.064973
DCSTAMP dendrocyte expressed seven transmembrane protein 0.064973
SMC2 structural maintenance of chromosomes 2 0.064973
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic) 0.064973
HPSE2 heparanase 2 (inactive) 0.043246
GMPR guanosine monophosphate reductase 0.035343