prolonged bleeding time Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Prolongation of the time taken for a standardized skin cut of fixed depth and length to stop bleeding. (Human Phenotype Ontology, HP_0003010)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003010
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Genes

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

Symbol Name
CD36 CD36 molecule (thrombospondin receptor)
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GATA1 GATA binding protein 1 (globin transcription factor 1)
GFI1B growth factor independent 1B transcription repressor
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP6 glycoprotein VI (platelet)
GP9 glycoprotein IX (platelet)
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)
MYH9 myosin, heavy chain 9, non-muscle
NBEAL2 neurobeachin-like 2
RASGRP2 RAS guanyl releasing protein 2 (calcium and DAG-regulated)
RIN2 Ras and Rab interactor 2
RUNX1 runt-related transcription factor 1
SOS1 son of sevenless homolog 1 (Drosophila)
TBXAS1 thromboxane A synthase 1 (platelet)
VWF von Willebrand factor
WAS Wiskott-Aldrich syndrome