platelet storage pool deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

31 genes co-occuring with the disease platelet storage pool deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HPS1 Hermansky-Pudlak syndrome 1 2.28838
BLOC1S6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin 1.9825
AP3B1 adaptor-related protein complex 3, beta 1 subunit 1.91547
HPS4 Hermansky-Pudlak syndrome 4 1.82957
HPS3 Hermansky-Pudlak syndrome 3 1.6986
BLOC1S5 biogenesis of lysosomal organelles complex-1, subunit 5, muted 1.34374
HPS6 Hermansky-Pudlak syndrome 6 1.23126
LYST lysosomal trafficking regulator 1.23082
BLOC1S3 biogenesis of lysosomal organelles complex-1, subunit 3 1.18927
SAR1A secretion associated, Ras related GTPase 1A 1.16949
RAP2B RAP2B, member of RAS oncogene family 1.16563
RAB27B RAB27B, member RAS oncogene family 1.16221
RAB1B RAB1B, member RAS oncogene family 1.16136
ARF3 ADP-ribosylation factor 3 1.14687
HPS5 Hermansky-Pudlak syndrome 5 1.13585
SNAPIN SNAP-associated protein 1.12151
RAB38 RAB38, member RAS oncogene family 1.03577
P2RX1 purinergic receptor P2X, ligand gated ion channel, 1 0.920085
PPBP pro-platelet basic protein (chemokine (C-X-C motif) ligand 7) 0.799923
RAB27A RAB27A, member RAS oncogene family 0.738676
CD63 CD63 molecule 0.680297
VWF von Willebrand factor 0.537344
PF4 platelet factor 4 0.527676
SFTPD surfactant protein D 0.486646
GPI glucose-6-phosphate isomerase 0.411283
EDN1 endothelin 1 0.382223
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 0.371477
F8 coagulation factor VIII, procoagulant component 0.355972
CA2 carbonic anhydrase II 0.325187
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) 0.214297
GUSB glucuronidase, beta 0.206913