periodontitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000704
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Genes

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

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
COL3A1 collagen, type III, alpha 1
CTSC cathepsin C
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
ELANE elastase, neutrophil expressed
FERMT1 fermitin family member 1
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
LYST lysosomal trafficking regulator
NOTCH2 notch 2
OCRL oculocerebrorenal syndrome of Lowe
PLG plasminogen
SLC35C1 solute carrier family 35 (GDP-fucose transporter), member C1
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase