increased mean platelet volume Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Average platelet volume above the upper limit of the normal reference interval. (Human Phenotype Ontology, HP_0011877)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011877
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Genes

14 genes associated with the increased mean platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
ACTN1 actinin, alpha 1
CD36 CD36 molecule (thrombospondin receptor)
FLNA filamin A, alpha
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP9 glycoprotein IX (platelet)
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LBR lamin B receptor
MYH9 myosin, heavy chain 9, non-muscle
SC5D sterol-C5-desaturase
TTC37 tetratricopeptide repeat domain 37