Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Clinical Features, Genetics and Potential Therapeutic Approaches for Birt-Hogg-Dubé Syndrome. 26581862 2019
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Cutaneous melanoma in Birt-Hogg-Dubé syndrome: part of the clinical spectrum? 28869776 2018
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. 28724667 2017
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt-Hogg-Dube syndrome prospectively detected by review of chest computed tomography scans. 28151982 2017
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome. 28558743 2017
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer. 28499369 2017
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation. 27734835 2017
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes. 27356891 2016
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome. 27220747 2016
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review. 26659639 2016
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt-Hogg-Dubé syndrome detected incidentally by asymptomatic bilateral pneumothorax in health screening: a case of a young Japanese woman. 26943385 2015
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Genetic analysis of familial spontaneous pneumothorax in an Indian family. 25827758 2015
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome. 25594584 2015
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Perifollicular fibromas associated with Birt-Hogg-Dubé syndrome. 26387484 2015
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Possible familial case of Birt-Hogg-Dubé syndrome complicated with lung cancer: A possible link between these two disease entities. 26028485 2015
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients. 24994497 2014
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR An oncocytic adrenal tumour in a patient with Birt-Hogg-Dubé syndrome. 23848572 2014
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt-Hogg-Dube syndrome is a novel ciliopathy. 23784378 2013
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Pneumothorax developing for the first time in a 73-year-old woman diagnosed with Birt-Hogg-Dubé syndrome. 24190151 2013
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR When the chest is clueless, look downstairs. 23741947 2013
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt-Hogg-Dubé syndrome: report of a new mutation. 22679611 2012
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations. 20618353 2011
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability. 21538689 2011
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Birt-hogg-dubé syndrome, a rare case in Korea confirmed by genetic analysis. 22148048 2011
Entrez Id: 23164
Gene Symbol: MPRIP
MPRIP
0.100 CausalMutation group CLINVAR Choroidal melanoma and lid fibrofoliculomas in Birt-Hogg-Dubé syndrome. 21401403 2011