Periodontal Pocket Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0031094
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Genes

28 genes associated with the disease Periodontal Pocket in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM8 ADAM metallopeptidase domain 8
CFH complement factor H
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
F2RL1 coagulation factor II (thrombin) receptor-like 1
FBLIM1 filamin binding LIM protein 1
FGF7 fibroblast growth factor 7
FGFR2 fibroblast growth factor receptor 2
GH1 growth hormone 1
GOPC golgi-associated PDZ and coiled-coil motif containing
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL22 interleukin 22
IL6 interleukin 6
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
LGALS9 lectin, galactoside-binding, soluble, 9
MPO myeloperoxidase
NR1I2 nuclear receptor subfamily 1, group I, member 2
PF4 platelet factor 4
PGLYRP1 peptidoglycan recognition protein 1
PLTP phospholipid transfer protein
RASA1 RAS p21 protein activator (GTPase activating protein) 1
RGS6 regulator of G-protein signaling 6
SLC52A1 solute carrier family 52 (riboflavin transporter), member 1
STAT1 signal transducer and activator of transcription 1, 91kDa
TNF tumor necrosis factor
TREM1 triggering receptor expressed on myeloid cells 1
UCN2 urocortin 2
WNT5A wingless-type MMTV integration site family, member 5A