gingival bleeding Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage affecting the gingiva. (Human Phenotype Ontology, HP_0000225)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000225
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Genes

20 genes associated with the gingival bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
F10 coagulation factor X
F2 coagulation factor II (thrombin)
FERMT1 fermitin family member 1
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
GBA glucosidase, beta, acid
GP1BA glycoprotein Ib (platelet), alpha polypeptide
HPS1 Hermansky-Pudlak syndrome 1
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
JAK2 Janus kinase 2
LYST lysosomal trafficking regulator
MPL MPL proto-oncogene, thrombopoietin receptor
MYD88 myeloid differentiation primary response 88
SCARB2 scavenger receptor class B, member 2
TET2 tet methylcytosine dioxygenase 2
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1