conical tooth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal conical form of the teeth, that is, a tooth whose sides converge or taper together incisally. (Human Phenotype Ontology, HP_0000698)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000698
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Genes

15 genes associated with the conical tooth 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
DHODH dihydroorotate dehydrogenase (quinone)
EDA ectodysplasin A
EVC Ellis van Creveld protein
FGF10 fibroblast growth factor 10
FGF3 fibroblast growth factor 3
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
NFKBIA nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
PVRL4 poliovirus receptor-related 4
SATB2 SATB homeobox 2
TP63 tumor protein p63
WNT10A wingless-type MMTV integration site family, member 10A