mediastinal lymphadenopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Swelling of lymph nodes within the mediastinum, the central compartment of the thoracic cavities that contains the heart and the great vessels, the esophagus, and trachea and other structures including lymph nodes. (Human Phenotype Ontology, HP_0100721)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100721
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Genes

20 genes associated with the mediastinal lymphadenopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
BCL2 B-cell CLL/lymphoma 2
BCL6 B-cell CLL/lymphoma 6
BIRC3 baculoviral IAP repeat containing 3
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
EWSR1 EWS RNA-binding protein 1
FOXP1 forkhead box P1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL6 interleukin 6
LEMD3 LEM domain containing 3
MALT1 MALT1 paracaspase
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NCF4 neutrophil cytosolic factor 4, 40kDa
PORCN porcupine homolog (Drosophila)
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
WT1 Wilms tumor 1