Periodontal Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

27 genes associated with the Periodontal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADRB3 adrenoceptor beta 3
BPI bactericidal/permeability-increasing protein
CAMP cathelicidin antimicrobial peptide
CXCR2 chemokine (C-X-C motif) receptor 2
DEFB1 defensin, beta 1
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
FCGR3B Fc fragment of IgG, low affinity IIIb, receptor (CD16b)
HBB hemoglobin, beta
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
IL10 interleukin 10
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1R1 interleukin 1 receptor, type I
IL1R2 interleukin 1 receptor, type II
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
IL6 interleukin 6
MPO myeloperoxidase
NOTCH3 notch 3
OSBPL10 oxysterol binding protein-like 10
PTGER3 prostaglandin E receptor 3 (subtype EP3)
TGFB1 transforming growth factor, beta 1
TLR2 toll-like receptor 2
TLR4 toll-like receptor 4
TNF tumor necrosis factor
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor