Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 Biomarker BEFREE IgG and IgA autoreactivity to BPI in CF patients was demonstrated in serum and BAL, respectively, and correlated with the isotype of the antibody response to P. aeruginosa. 31262645

2019

Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 AlteredExpression BEFREE In the CF group, platelet aggregation correlates with levels of anti-neutrophil cytoplasmic antibodies (ANCA) with specificity for bactericidal/permeability-increasing protein (BPI), BPI-ANCA (r=0.56). 29274562

2018

Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 Biomarker BEFREE The presence of BPI-ANCA was associated with the number of antibiotic courses, low body mass index, Pseudomonas aeruginosa colonisation, the presence of resistant P. aeruginosa, low forced expiratory volume in 1 s, CF-related liver disease, hypergammaglobulinaemia, male sex and inflammatory syndrome. 19443536

2009

Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 AlteredExpression LHGDN Thus, BPI that is functionally active against mucoid P. aeruginosa strains is expressed in the airways of CF patients but may be hampered by autoantibodies, resulting in chronic infection. 16861658

2006

Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 Biomarker BEFREE BPI represents a major ANCA target antigen in patients with rheumatological as well as inflammatory bowel disease and cystic fibrosis, but AZ-ANCA are uncommon. 10836522

2000

Entrez Id: 671
Gene Symbol: BPI
BPI
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.060 Biomarker BEFREE Circulating ANCA specific for bactericidal/permeability increasing protein (BPI) have been recently reported in adult patients with cystic fibrosis (CF), an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane regulator (CFTR) gene with consequent impaired function of a transmembrane chloride channel. 9650098

1998