Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE Treatment-related complications occurred more frequently in the advanced GAP stage group; advanced GAP stage was the only predictor that exhibited a significant association with the incidence of acute exacerbation of IPF. 31186636

2019

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE We aimed to determine the efficacy of LC treatments and the prognosis in LC patients with IPF according to the LC stage and GAP (gender [G], age [A], and two physiology variables [P]) stage. 31467375

2019

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE CONCLUSIONS Spirometry, GAP model, and BAL are helpful to forecast the prognosis of IPF. 31166938

2019

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE Multi-dimensional scores (Composite Physiologic index [CPI], [Gender-Age-Physiology [GAP]; RIsk Stratification scorE [RISE]) demonstrated enhanced predictive power towards outcome in IPF. 28340864

2017

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE The percentage of aTregs was correlated negatively with predicted diffusing capacity values for carbon monoxide and positively with GAP index in IPF. 28886713

2017

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE GAP and ILD-GAP are applicable for evaluating the risk of death of patients with RA-ILD in a similar manner as in those with IPF. 28086844

2017

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE Both the revised J-system and the modified GAP system are independent and valuable tools for prognostication and clinical management for IPF. 28787101

2017

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE Correlation coefficients between the baseline level of Diffuse Lung Capacity for Carbon monoxide (DLCO), Forced Vital Capacity (FVC), 6MWD, power developed during incremental endurance test, GAP index (in IPF patients only) and etiology (IPF or non-IPF) with the functional improvement at the 6MWDT (meters), at the incremental and endurance cyclo-ergometry (endurance time) and the HRQoL were assessed. 29017478

2017

Entrez Id: 9628
Gene Symbol: RGS6
RGS6
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.090 Biomarker BEFREE The GAP model that was derived for IPF performs similarly as a mortality risk prediction tool in RA-ILD. 28502419

2017