neoplasm of the respiratory system Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tumor (abnormal growth of tissue) of the respiratory system. (Human Phenotype Ontology, HP_0100606)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100606
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Genes

37 genes associated with the neoplasm of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)
BRAF B-Raf proto-oncogene, serine/threonine kinase
CHEK2 checkpoint kinase 2
DICER1 dicer 1, ribonuclease type III
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
DLEC1 deleted in lung and esophageal cancer 1
EGFR epidermal growth factor receptor
ERBB2 erb-b2 receptor tyrosine kinase 2
EWSR1 EWS RNA-binding protein 1
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
IGHV4-34 immunoglobulin heavy variable 4-34
IRF1 interferon regulatory factor 1
KRAS Kirsten rat sarcoma viral oncogene homolog
MAP3K8 mitogen-activated protein kinase kinase kinase 8
MBTPS2 membrane-bound transcription factor peptidase, site 2
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NOTCH3 notch 3
PARK2 parkin RBR E3 ubiquitin protein ligase
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
POU6F2 POU class 6 homeobox 2
PPP2R1B protein phosphatase 2, regulatory subunit A, beta
PTEN phosphatase and tensin homolog
RASSF1 Ras association (RalGDS/AF-6) domain family member 1
SFTPA2 surfactant protein A2
SLC22A18 solute carrier family 22, member 18
SLCO2A1 solute carrier organic anion transporter family, member 2A1
STK11 serine/threonine kinase 11
TP53 tumor protein p53
TRPV3 transient receptor potential cation channel, subfamily V, member 3
WRN Werner syndrome, RecQ helicase-like
WT1 Wilms tumor 1