Hyperostosis Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A bone remodeling disease that results in an abnormal growth of located_in bone. (Human Disease Ontology, DOID_205)
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Genes

24 genes associated with the disease Hyperostosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
GSTM3 glutathione S-transferase mu 3 (brain) 1.954
EPS8L3 EPS8-like 3 1.954
GSTM5 glutathione S-transferase mu 5 1.954
CCDC3 coiled-coil domain containing 3 1.944
OPTN optineurin 1.944
MCM10 minichromosome maintenance complex component 10 1.944
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator 1.885
RIMS2 regulating synaptic membrane exocytosis 2 1.76
DPYS dihydropyrimidinase 1.76
DCSTAMP dendrocyte expressed seven transmembrane protein 1.76
PML promyelocytic leukemia 1.678
STOML1 stomatin (EPB72)-like 1 1.678
ISLR2 immunoglobulin superfamily containing leucine-rich repeat 2 1.678
LOXL1 lysyl oxidase-like 1 1.678
GOLGA6A golgin A6 family, member A 1.678
RIN3 Ras and Rab interactor 3 1.448
LGMN legumain 1.448
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 1.448
CNOT4 CCR4-NOT transcription complex, subunit 4 1.285
SLC13A4 solute carrier family 13 (sodium/sulfate symporter), member 4 1.285
NUP205 nucleoporin 205kDa 1.285
STMP1 short transmembrane mitochondrial protein 1 1.285
CSF1 colony stimulating factor 1 (macrophage) 1.231
RELCH RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing 0.8