Ossifying Fibroma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A bone benign neoplasm that is located_in the mouth and results_in an overgrowth of gingival tissue due to irritation or trauma. (Human Disease Ontology, DOID_180)
External Link https://www.disgenet.org/browser/0/1/0/C0206640
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Genes

16 genes associated with the disease Ossifying Fibroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CD34 CD34 molecule
CD6 CD6 molecule
CDC73 cell division cycle 73
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
GNAS GNAS complex locus
HMMR hyaluronan-mediated motility receptor (RHAMM)
MCM2 minichromosome maintenance complex component 2
MCM7 minichromosome maintenance complex component 7
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase
MEN1 multiple endocrine neoplasia I
PTH parathyroid hormone
RASAL1 RAS protein activator like 1 (GAP1 like)
RUNX2 runt-related transcription factor 2
SMAD3 SMAD family member 3
WWOX WW domain containing oxidoreductase
ZC3HAV1 zinc finger CCCH-type, antiviral 1