Mediastinal Lymphadenopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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 https://www.disgenet.org/browser/0/1/0/C0520743
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Genes

19 genes associated with the disease Mediastinal Lymphadenopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
BCL10 B-cell CLL/lymphoma 10
BCL2 B-cell CLL/lymphoma 2
BCL6 B-cell CLL/lymphoma 6
BIRC3 baculoviral IAP repeat containing 3
C17ORF62 chromosome 17 open reading frame 62
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
IGH immunoglobulin heavy locus
MALT1 MALT1 paracaspase
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NCF4 neutrophil cytosolic factor 4, 40kDa
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
WT1 Wilms tumor 1