abnormality of incisor morphology Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of morphology of the incisor tooth. (Human Phenotype Ontology, HP_0011063)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011063
Similar Terms
Downloads & Tools

Genes

12 genes associated with the abnormality of incisor morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
B3GALTL	beta 1,3-galactosyltransferase-like
CCBE1	collagen and calcium binding EGF domains 1
CHSY1	chondroitin sulfate synthase 1
COL11A1	collagen, type XI, alpha 1
CREBBP	CREB binding protein
FGF10	fibroblast growth factor 10
FGFR2	fibroblast growth factor receptor 2
FGFR3	fibroblast growth factor receptor 3
IKBKG	inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
NHS	Nance-Horan syndrome (congenital cataracts and dental anomalies)
VPS13B	vacuolar protein sorting 13 homolog B (yeast)
WNT10A	wingless-type MMTV integration site family, member 10A