abnormality of the dental pulp Gene Set
Genes
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
|
