Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 Biomarker disease BEFREE The overall incidence of grade I-IV aGVHD was 40.4%. 31537901 2020
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 Biomarker disease BEFREE Multivariate analyses identified the absolute number of MAIT cells (< 0.48/μL on day 60 post-HSCT) as the sole independent risk factor for grade I-IV and grade II-IV acute graft-versus-host disease (aGVHD) among patients who underwent bone marrow transplantation; no correlation was observed between post-HSCT iNKT cell recovery and the development of aGVHD. 29582333 2018
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 Biomarker disease BEFREE Thirty-two had grade I-IV aGVHD with incidence of 51.61%. 29744996 2018
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 Biomarker disease BEFREE The incidence of aGvHD (grades I-IV) was lower in patients having A allele (52/119 vs. 113/204, p=0.043) and AA homozygous genotype (6/25 vs. 159/298, p=0.005). 25982843 2015
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 GeneticVariation disease BEFREE Furthermore, patients who received grafts from donors with an IL-10 -819 CC genotype experienced more frequent grade I-IV aGVHD (OR, 2.306 (95% CI, 1.168-4.551)). 25116082 2015
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 GeneticVariation disease BEFREE Our meta-analysis combined the results of several studies and demonstrated that the donor IL-6 G allele is associated with an increased risk of grades I-IV and II-IV aGVHD. 22304944 2012
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 Biomarker disease BEFREE Ten patients developed acute GVHD (grade I-IV) and one developed chronic GVHD, which were controlled by induction of the suicide gene. 19345145 2009
Entrez Id: 80316
Gene Symbol: PPP1R2C
PPP1R2C
0.080 GeneticVariation disease BEFREE Recipients carrying the CCR5Delta32 allele developed acute GvHD (grades I-IV) less frequently than did patients lacking the CCR5 deletion mutation (11/35 vs. 76/151, p=0.033). 17145599 2006