Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 Biomarker disease GENOMICS_ENGLAND Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis. 25425184 2014
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 Biomarker disease GENOMICS_ENGLAND GM-CSF-dependent pSTAT5 sensitivity is a feature with therapeutic potential in chronic myelomonocytic leukemia. 23632888 2013
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 GeneticVariation disease UNIPROT Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA. 18955570 2008
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 GeneticVariation disease UNIPROT Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1. 18955567 2008
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 Biomarker disease CTD_human
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 CausalMutation disease CLINVAR
Entrez Id: 1438
Gene Symbol: CSF2RA
CSF2RA 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1437
Gene Symbol: CSF2
CSF2 		0.010 Biomarker disease BEFREE Hereditary pulmonary alveolar proteinosis (hPAP) caused by granulocyte-macrophage colony-stimulating factor (GM-CSF) receptor α-chain (CSF2RA) deficiency is a rare, life-threatening lung disease characterized by accumulation of proteins and phospholipids in the alveolar spaces. 24279725 2014