USP40, ubiquitin specific peptidase 40, 55230

N. diseases: 5; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation phenotype GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.100 GeneticVariation phenotype GWASDB Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. 21646302 2011
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.100 GeneticVariation phenotype GWASCAT Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. 21646302 2011
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.100 GeneticVariation phenotype GWASDB Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. 21646302 2011
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.100 GeneticVariation phenotype GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.100 GeneticVariation phenotype GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 Biomarker disease BEFREE The present study is the first to report a lack of association between SNPs of USP24 and USP40 and PD in Han Chinese patients. 22923019 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 Biomarker disease BEFREE Our results suggest that USP24 alone plays a role in PD susceptibility among Taiwanese people >or=60 years of age, or acting synergistically with USP40 and UCHL1 in the total subjects. 20302855 2010
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 GeneticVariation disease LHGDN Our data suggest that genetic variants in USP24 and USP40 affect the risk for late-onset PD, which is consistent with the predicted role of the ubiquitination pathway in PD etiology. 16917932 2006
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
PARKINSON DISEASE, LATE-ONSET 		0.010 GeneticVariation disease BEFREE Our data suggest that genetic variants in USP24 and USP40 affect the risk for late-onset PD, which is consistent with the predicted role of the ubiquitination pathway in PD etiology. 16917932 2006