abnormality of dentin Gene Set
Genes
12 genes associated with the abnormality of dentin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
COL1A1
|
collagen, type I, alpha 1
|
COL1A2
|
collagen, type I, alpha 2
|
DSPP
|
dentin sialophosphoprotein
|
FKBP10
|
FK506 binding protein 10, 65 kDa
|
IFT122
|
intraflagellar transport 122
|
IFT43
|
intraflagellar transport 43
|
OCRL
|
oculocerebrorenal syndrome of Lowe
|
PPIB
|
peptidylprolyl isomerase B (cyclophilin B)
|
SERPINH1
|
serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
|
WDR19
|
WD repeat domain 19
|
WDR35
|
WD repeat domain 35
|
ZNF469
|
zinc finger protein 469
|