abnormality of dentin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of dentin. (Human Phenotype Ontology, HP_0010299)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010299
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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
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