dental caries Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. The three most prominent theories used to explain the etiology of the disease are that acids produced by bacteria lead to decalcification; that micro-organisms destroy the enamel protein; or that keratolytic micro-organisms produce chelates that lead to decalcification. (Experimental Factor Ontology, EFO_0003819)
Similar Terms
Downloads & Tools

Genes

14 genes associated with the disease dental caries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AMBN ameloblastin (enamel matrix protein)
AMELX amelogenin, X-linked
ENAM enamelin
GNAT3 guanine nucleotide binding protein, alpha transducing 3
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
LTF lactotransferrin
MBL2 mannose-binding lectin (protein C) 2, soluble
MPPED2 metallophosphoesterase domain containing 2
MTMR4 myotubularin related protein 4
TAS1R2 taste receptor, type 1, member 2
TAS2R38 taste receptor, type 2, member 38
TFIP11 tuftelin interacting protein 11
TUFT1 tuftelin 1