increased number of teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a supernumerary, i.e., extra, tooth or teeth. (Human Phenotype Ontology, HP_0011069)
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20 genes associated with the increased number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
AMMECR1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
APC adenomatous polyposis coli
BCOR BCL6 corepressor
C2CD3 C2 calcium-dependent domain containing 3
CCBE1 collagen and calcium binding EGF domains 1
DHCR7 7-dehydrocholesterol reductase
EXT1 exostosin glycosyltransferase 1
FAT4 FAT atypical cadherin 4
FGF3 fibroblast growth factor 3
IL11RA interleukin 11 receptor, alpha
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
OFD1 oral-facial-digital syndrome 1
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
RECQL4 RecQ protein-like 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
RUNX2 runt-related transcription factor 2
TRPS1 trichorhinophalangeal syndrome I
WNT5A wingless-type MMTV integration site family, member 5A