COPG1, COPI coat complex subunit gamma 1, 22820

N. diseases: 4; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma 		0.310 GeneticVariation disease BEFREE BAP1 and COPG1 mutations were seen exclusively in MM. 26463840 2016
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma 		0.310 Biomarker disease CTD_human BAP1 and COPG1 mutations were seen exclusively in MM. 26463840 2016
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation phenotype GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.100 GeneticVariation phenotype GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
CUI: C0017638
Disease: Glioma
Glioma 		0.010 Biomarker disease BEFREE Six genes independently correlated with either age (IL-6, TNFRSF-11B, IGFBP-3, SAA4, and COPG), prognosis (IL-6, SAA4), or the grade of the glioma (IL-6, IL-8, ICAM-1, IGFBP-3, and COPG). 25220188 2014