Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 726
Gene Symbol: CAPN5
CAPN5
0.710 GeneticVariation disease UNIPROT Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration. 23055945 2012
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.090 GeneticVariation disease BEFREE Differences in genotype distributions between patients with RRD with or without PVR were detected in rs1800795 (IL6) (P = 0.04), rs1800871 (in the vicinity of the IL10) (P = 0.034), and rs1800471 (TGFB1) (P = 0.032). 30807515 2019
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.090 GeneticVariation disease BEFREE Differences in genotype distributions between patients with RRD with or without PVR were detected in rs1800795 (IL6) (P = 0.04), rs1800871 (in the vicinity of the IL10) (P = 0.034), and rs1800471 (TGFB1) (P = 0.032). 30807515 2019
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.090 GeneticVariation disease BEFREE Vitreous concentrations of interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 1 beta (IL-1 β), tumor necrosis factor beta (TNF-β), granulocyte macrophage colony stimulating factor (GM-CSF), interferon gamma (IFN-γ), C reactive protein; (CRP), placental growth factor (PlGF), platelet derived growth factor BB (PDGF-BB), vascular endothelial growth factor (VEGF) and angiopoietin 2 (Ang-2) at weeks 2, 3 and 4 were compared to baseline and correlations between the cytokines with PVR severity were assessed. 31659187 2019
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.060 GeneticVariation disease BEFREE These results confirm the genetic contribution to PVR and the implication of SMAD7 and TNF locus in the development of PVR. 23258148 2013
Entrez Id: 4193
Gene Symbol: MDM2
MDM2
0.060 GeneticVariation disease BEFREE The purpose was to evaluate the impact of T309G MDM2 polymorphism (rs2279744) in PVR. 24349246 2013
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.060 GeneticVariation disease BEFREE Blood from 450 patients with (138 cases) and without (312 controls) post-rhegmatogenous retinal detachment (RD) PVR was genotyped to determine polymorphisms located in the TNFα gene. 20663564 2010
Entrez Id: 4193
Gene Symbol: MDM2
MDM2
0.060 GeneticVariation disease BEFREE Furthermore, our experimental results demonstrated that MDM2 T309G in hPRPE cells enhanced vitreous-induced cell proliferation and survival, suggesting that this SNP contributes to the pathogenesis of PVR. 27246850 2016
Entrez Id: 5294
Gene Symbol: PIK3CG
PIK3CG
0.050 GeneticVariation disease BEFREE After correction for multiple comparisons, four genes were significantly associated with PVR: SMAD7 (P = 0.004), PIK3CG (P = 0.009), TNF locus (P = 0.0005), and TNFR2 (P = 0.019) In the European sample, replication was observed in SMAD7 (P = 0.047) and the TNF locus (P = 0.044). 23258148 2013
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.050 GeneticVariation disease BEFREE The murine double minute (MDM)2 is a critical negative regulator of the p53 tumor suppressor, and MDM2 SNP309G is associated with a higher risk of proliferative vitreoretinopathy (PVR); in addition, the MDM2 T309G created using clustered regularly interspaced short palindromic repeats (CRISPR)/associated endonuclease (Cas)9 enhances normal rabbit vitreous-induced expression of MDM2 and survival of primary human retinal pigment epithelial (hRPE) cells in vitro. 29049737 2017
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.050 GeneticVariation disease BEFREE The C allele for rs1042522 in p53 was genetically associated with a higher risk for RD but not for PVR in this cohort. 28106707 2018
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.050 GeneticVariation disease BEFREE Results indicate that the Pro variant of p53 codon 72 polymorphism is associated with a higher risk of PVR developing after a primary RD. 23207172 2013
Entrez Id: 4049
Gene Symbol: LTA
LTA
0.030 GeneticVariation disease BEFREE Vitreous concentrations of interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 1 beta (IL-1 β), tumor necrosis factor beta (TNF-β), granulocyte macrophage colony stimulating factor (GM-CSF), interferon gamma (IFN-γ), C reactive protein; (CRP), placental growth factor (PlGF), platelet derived growth factor BB (PDGF-BB), vascular endothelial growth factor (VEGF) and angiopoietin 2 (Ang-2) at weeks 2, 3 and 4 were compared to baseline and correlations between the cytokines with PVR severity were assessed. 31659187 2019
Entrez Id: 4049
Gene Symbol: LTA
LTA
0.030 GeneticVariation disease BEFREE The strong association found in the rs2229094(T→C) of the LTA gene may indicate an important role of this polymorphism in the development of PVR. 20663564 2010
Entrez Id: 4092
Gene Symbol: SMAD7
SMAD7
0.020 GeneticVariation disease BEFREE These results confirm the genetic contribution to PVR and the implication of SMAD7 and TNF locus in the development of PVR. 23258148 2013
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.020 GeneticVariation disease BEFREE Vitreous concentrations of interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 1 beta (IL-1 β), tumor necrosis factor beta (TNF-β), granulocyte macrophage colony stimulating factor (GM-CSF), interferon gamma (IFN-γ), C reactive protein; (CRP), placental growth factor (PlGF), platelet derived growth factor BB (PDGF-BB), vascular endothelial growth factor (VEGF) and angiopoietin 2 (Ang-2) at weeks 2, 3 and 4 were compared to baseline and correlations between the cytokines with PVR severity were assessed. 31659187 2019
Entrez Id: 1437
Gene Symbol: CSF2
CSF2
0.020 GeneticVariation disease BEFREE Vitreous concentrations of interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 1 beta (IL-1 β), tumor necrosis factor beta (TNF-β), granulocyte macrophage colony stimulating factor (GM-CSF), interferon gamma (IFN-γ), C reactive protein; (CRP), placental growth factor (PlGF), platelet derived growth factor BB (PDGF-BB), vascular endothelial growth factor (VEGF) and angiopoietin 2 (Ang-2) at weeks 2, 3 and 4 were compared to baseline and correlations between the cytokines with PVR severity were assessed. 31659187 2019
Entrez Id: 3586
Gene Symbol: IL10
IL10
0.010 GeneticVariation disease BEFREE Differences in genotype distributions between patients with RRD with or without PVR were detected in rs1800795 (IL6) (P = 0.04), rs1800871 (in the vicinity of the IL10) (P = 0.034), and rs1800471 (TGFB1) (P = 0.032). 30807515 2019
Entrez Id: 2091
Gene Symbol: FBL
FBL
0.010 GeneticVariation disease BEFREE The secondary outcome was to observe dynamic changes of the FIB-4 index between CVR patients and PVR patients. 26604649 2015
Entrez Id: 7133
Gene Symbol: TNFRSF1B
TNFRSF1B
0.010 GeneticVariation disease BEFREE After correction for multiple comparisons, four genes were significantly associated with PVR: SMAD7 (P = 0.004), PIK3CG (P = 0.009), TNF locus (P = 0.0005), and TNFR2 (P = 0.019) In the European sample, replication was observed in SMAD7 (P = 0.047) and the TNF locus (P = 0.044). 23258148 2013
Entrez Id: 581
Gene Symbol: BAX
BAX
0.010 GeneticVariation disease BEFREE To compare the distribution of BCL-2 -938C>A (rs2279115) and BAX -248G>A (rs4645878) genotypes among European subjects undergoing rhegmatogenous retinal detachment (RRD) surgery in relation to the further development of proliferative vitreoretinopathy (PVR). 25991504 2015
Entrez Id: 726
Gene Symbol: CAPN5
CAPN5
0.710 Biomarker disease BEFREE The CAPN5-NIV vitreous proteome displayed characteristic enrichment of proteins and pathways previously-associated with non-infectious posterior uveitis, rhegmatogenous retinal detachment (RRD), age-related macular degeneration (AMD), proliferative diabetic retinopathy (PDR), and proliferative vitreoretinopathy (PVR). 31110225 2019
Entrez Id: 726
Gene Symbol: CAPN5
CAPN5
0.710 Biomarker disease CTD_human
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.300 Biomarker disease CTD_human A model for familial exudative vitreoretinopathy caused by LPR5 mutations. 18263894 2008
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.090 Biomarker disease LHGDN There was a higher frequency of TGF-beta1 codon 10 allele T in PVR patients compared with RD patients (p = 0.023). 16704689 2006