abnormality of permanent molar morphology Gene Set
Genes
19 genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
DLX3
|
distal-less homeobox 3
|
|
EDA
|
ectodysplasin 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
|
