myelofibrosis Gene Set

Dataset MPO Gene-Phenotype 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://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011747
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Genes

7 gene mutations causing the myelofibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID4A AT rich interactive domain 4A (RBP1-like)
C6ORF25 chromosome 6 open reading frame 25
CLCN7 chloride channel, voltage-sensitive 7
ESR2 estrogen receptor 2 (ER beta)
GATA1 GATA binding protein 1 (globin transcription factor 1)
NCOR2 nuclear receptor corepressor 2
STIM1 stromal interaction molecule 1