myelofibrosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A myeloma that is located_in the bone marrow which results_in bone marrow being replaced by fibrous (scar) tissue. (Human Disease Ontology, DOID_4971)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011974
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Genes

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

Symbol Name
CALR calreticulin
GFI1B growth factor independent 1B transcription repressor
JAK2 Janus kinase 2
MPL MPL proto-oncogene, thrombopoietin receptor
NBEAL2 neurobeachin-like 2
SH2B3 SH2B adaptor protein 3
TBXAS1 thromboxane A synthase 1 (platelet)