oligodontia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tooth disease characterized by failure to develop on or more missing teeth. (Human Disease Ontology, DOID_0050591)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000677
Similar Terms
Downloads & Tools

Genes

16 genes associated with the oligodontia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
AXIN2 axin 2
BCOR BCL6 corepressor
CCBE1 collagen and calcium binding EGF domains 1
CLDN1 claudin 1
EDA ectodysplasin A
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
LTBP3 latent transforming growth factor beta binding protein 3
PAX9 paired box 9
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
PORCN porcupine homolog (Drosophila)
PTHLH parathyroid hormone-like hormone
SATB2 SATB homeobox 2
SH3BP2 SH3-domain binding protein 2
TP63 tumor protein p63