abnormality of the mediastinum Gene Set
Genes
20 genes associated with the abnormality of the mediastinum 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
|
