thrombocytosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A myeloma and blood platelet disease that is characterized by the presence of high platelet counts in the blood. (Human Disease Ontology, DOID_2228)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001894
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Genes

12 genes associated with the thrombocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CALR calreticulin
CECR1 cat eye syndrome chromosome region, candidate 1
ELANE elastase, neutrophil expressed
JAK2 Janus kinase 2
MPL MPL proto-oncogene, thrombopoietin receptor
PMM2 phosphomannomutase 2
RPS19 ribosomal protein S19
RPSA ribosomal protein SA
SH2B3 SH2B adaptor protein 3
THPO thrombopoietin
TMEM173 transmembrane protein 173
TTC37 tetratricopeptide repeat domain 37