abnormality of the incisor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the Incisor tooth. (Human Phenotype Ontology, HP_0000676)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000676
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24 genes associated with the abnormality of the incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
ANKRD11 ankyrin repeat domain 11
ATRX alpha thalassemia/mental retardation syndrome X-linked
B3GALTL beta 1,3-galactosyltransferase-like
BCOR BCL6 corepressor
BLM Bloom syndrome, RecQ helicase-like
CCBE1 collagen and calcium binding EGF domains 1
CHSY1 chondroitin sulfate synthase 1
COL11A1 collagen, type XI, alpha 1
CREBBP CREB binding protein
EIF4A3 eukaryotic translation initiation factor 4A3
EVC Ellis van Creveld protein
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GLI2 GLI family zinc finger 2
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
PTCH1 patched 1
SHH sonic hedgehog
SIX3 SIX homeobox 3
VPS13B vacuolar protein sorting 13 homolog B (yeast)
WNT10A wingless-type MMTV integration site family, member 10A