abnormality of the dental pulp Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the dental pulp. (Human Phenotype Ontology, HP_0006479)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006479
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21 genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DLX3 distal-less homeobox 3
DSPP dentin sialophosphoprotein
EDA ectodysplasin A
FAM20A family with sequence similarity 20, member A
FGF10 fibroblast growth factor 10
FGF23 fibroblast growth factor 23
FGF3 fibroblast growth factor 3
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLII flightless I homolog (Drosophila)
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GJA1 gap junction protein, alpha 1, 43kDa
IFT122 intraflagellar transport 122
IFT43 intraflagellar transport 43
KL klotho
OCRL oculocerebrorenal syndrome of Lowe
RAI1 retinoic acid induced 1
SMOC2 SPARC related modular calcium binding 2
TP63 tumor protein p63
WDR19 WD repeat domain 19
WDR35 WD repeat domain 35