Splenomegaly Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal increased size of the spleen. (Human Phenotype Ontology, HP_0001744)
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Genes

19 genes associated with the Splenomegaly phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CALR calreticulin
CTLA4 cytotoxic T-lymphocyte-associated protein 4
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
HBA1 hemoglobin, alpha 1
HFE hemochromatosis
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMOX1 heme oxygenase 1
ICOS inducible T-cell co-stimulator
JAK2 Janus kinase 2
KDR kinase insert domain receptor
MPL MPL proto-oncogene, thrombopoietin receptor
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
TNFSF13 tumor necrosis factor (ligand) superfamily, member 13
VEGFA vascular endothelial growth factor A