abnormal number of incisors Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an altered number of of the incisor teeth.. (Human Phenotype Ontology, HP_0011064)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011064
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12 genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
B3GALTL beta 1,3-galactosyltransferase-like
BCOR BCL6 corepressor
BLM Bloom syndrome, RecQ helicase-like
EIF4A3 eukaryotic translation initiation factor 4A3
EVC Ellis van Creveld protein
GLI2 GLI family zinc finger 2
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