dentinogenesis imperfecta Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_4154)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000703
Similar Terms
Downloads & Tools

Genes

7 genes associated with the dentinogenesis imperfecta 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
PPIB peptidylprolyl isomerase B (cyclophilin B)
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
ZNF469 zinc finger protein 469