abnormality of the thoracic cavity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0045027
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Genes

20 genes associated with the abnormality of the thoracic cavity 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