Primary Myelofibrosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:D055728
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Genes

5 genes/proteins associated with the disease Primary Myelofibrosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
JAK2 Janus kinase 2 2.88009
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit 2.88009
TNF tumor necrosis factor 1.53796
COL1A2 collagen, type I, alpha 2 1.07625
IL6 interleukin 6 1.04868