Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.080 GeneticVariation disease BEFREE Our results reveal that SNP rs2664538, which is located at the MMP9 gene, is likely to be associated with acute PACG. 17110919 2006
Entrez Id: 3552
Gene Symbol: IL1A
IL1A
0.010 GeneticVariation disease BEFREE There was no significant difference in IL-1 SNP or allele frequencies for in subjects with POAG or PACG compared with control subjects, or between NTG and HTG. 17460270 2007
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.010 GeneticVariation disease BEFREE There was no significant difference in IL-1 SNP or allele frequencies for in subjects with POAG or PACG compared with control subjects, or between NTG and HTG. 17460270 2007
Entrez Id: 80207
Gene Symbol: OPA3
OPA3
0.010 Biomarker disease BEFREE No novel or previously reported mutations were present in the nuclear genes MYOC, OPTN, CYP1B1, WDR36, OPA1, and OPA3 in 29 patients with PACG. 18055808 2007
Entrez Id: 4016
Gene Symbol: LOXL1
LOXL1
0.010 Biomarker disease BEFREE The SNPs of LOXL1 did not exhibit any significant association with POAG or PACG, unlike previous studies from Icelandic, Swedish, U.S., and Australian populations with XFS/XFG. 18223248 2008
Entrez Id: 2944
Gene Symbol: GSTM1
GSTM1
0.010 GeneticVariation disease BEFREE We compared the prevalence of GSTT1 and GSTM1 deletion genotypes, which were determined by multiplex polymerase chain reaction, in 107 Arab patients with glaucoma (49 with primary open-angle glaucoma, 29 with pseudoexfoliation glaucoma, and 29 with primary angle-closure glaucoma) to 120 age, sex, and ethnically matched controls. 18334963 2008
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.080 GeneticVariation disease BEFREE This study did not find an association between the rs2664538 polymorphism within the MMP-9 gene and PACG in this sample of Chinese subjects. 18552608 2008
Entrez Id: 83552
Gene Symbol: MFRP
MFRP
0.040 Biomarker disease BEFREE To investigate the possible involvement of CHX10 and MFRP in PACG, we sequenced both genes in PACG patients with small ocular dimensions. 18648522 2008
Entrez Id: 338917
Gene Symbol: VSX2
VSX2
0.010 Biomarker disease BEFREE To investigate the possible involvement of CHX10 and MFRP in PACG, we sequenced both genes in PACG patients with small ocular dimensions. 18648522 2008
Entrez Id: 6678
Gene Symbol: SPARC
SPARC
0.020 AlteredExpression disease BEFREE The PACG iris expressed SPARC 13.6-fold more and collagen I 5.2 fold more compared to non-glaucoma control iris. 18949063 2008
Entrez Id: 348
Gene Symbol: APOE
APOE
0.010 GeneticVariation disease BEFREE The frequencies of apolipoprotein E (APOE) alleles and genotypes were examined in 230 Saudi subjects including primary open-angle glaucoma (POAG; n=60) and primary angle-closure glaucoma (PACG; n=40) patients as well as 130 control subjects. 19421411 2009
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.080 GeneticVariation disease BEFREE In contrast, the SNP rs17576 in MMP-9 might not be related to PACG in the same population. 19633731 2009
Entrez Id: 10203
Gene Symbol: CALCRL
CALCRL
0.020 GeneticVariation disease BEFREE To determine whether the polymorphisms of calcitonin receptor-like receptor gene (CALCRL) are associated with primary angle closure glaucoma (PACG) in a southern Chinese population. 19898635 2009
Entrez Id: 4909
Gene Symbol: NTF4
NTF4
0.020 GeneticVariation disease BEFREE Resequencing of NTF4 revealed a nonsynonymous (A88V), silent (P151P) and two changes in the 3'UTR region, along with a known polymorphism (rs11669977) in cases of POAG; the PACG cases exhibited only the A88V variation. 20463313 2010
Entrez Id: 110599580
Gene Symbol: LOC110599580
LOC110599580
0.010 Biomarker disease BEFREE We resequenced the CYP1B1 promoter in a large cohort (n = 835) that included patients with PCG (n = 301), other primary glaucomas (primary open-angle glaucoma: n = 115 and primary angle closure glaucoma: n = 100) and unaffected controls (n = 319). 20660114 2010
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.080 GeneticVariation disease BEFREE This study demonstrates an association between MMP9 SNPs rs3918249 and rs17576 and PACG in the Australian population, suggesting MMP9 may be involved in the pathogenesis of this blinding disease. 21655354 2011
Entrez Id: 3082
Gene Symbol: HGF
HGF
0.040 GeneticVariation disease BEFREE Genetic variation in HGF is associated with PACG in the Nepalese population. 21897747 2011
Entrez Id: 83552
Gene Symbol: MFRP
MFRP
0.040 GeneticVariation disease BEFREE SNPs in the nanophthalmos gene MFRP were found to be nominally associated with PACG under the allelic model. 22933837 2012
Entrez Id: 10203
Gene Symbol: CALCRL
CALCRL
0.020 GeneticVariation disease BEFREE This study implicates genetic variation at the CALCRL gene in the pathogenesis of PACG in an Australian Caucasian cohort. 22933837 2012
Entrez Id: 4909
Gene Symbol: NTF4
NTF4
0.020 GeneticVariation disease BEFREE In the Nepalese cohort, SNPs in CYP1B1 and NTF4 genes showed borderline association with PACG, but did not survive Bonferroni correction. 23422825 2013
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.020 GeneticVariation disease BEFREE In the Australian cohort, one eNOS SNP rs3793342 showed significance association with PACG after Bonferroni correction (P value of 0.003, odds ratio [OR] 0.5, 95% confidence interval [CI] 0.3-0.8). 23422825 2013
Entrez Id: 1545
Gene Symbol: CYP1B1
CYP1B1
0.010 GeneticVariation disease BEFREE In the Nepalese cohort, SNPs in CYP1B1 and NTF4 genes showed borderline association with PACG, but did not survive Bonferroni correction. 23422825 2013
Entrez Id: 1555
Gene Symbol: CYP2B6
CYP2B6
0.010 Biomarker disease BEFREE Recently, several studies have investigated genetic associations between Cytochrome P450 (CYP1B1), Endothelial nitric oxide synthase (eNOS), and Neurotrophin-4 (NTF4) with primary angle-closure glaucoma (PACG) in various ethnic groups. 23422825 2013
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.080 GeneticVariation disease BEFREE In addition, a significant difference was observed in genotype frequencies of MMP9 rs17576 (c.836A>G) in patients with PACG compared to the control subjects (p < 0.001), which after gender stratification remained significant in men (p = 0.009) but not in women (p = 0.14). 23441116 2013
Entrez Id: 4312
Gene Symbol: MMP1
MMP1
0.010 GeneticVariation disease BEFREE Our data suggest that the MMP1 rs1799750 (-1607 1G/2G) and MMP9 rs17576 polymorphisms might be of value for further study as potential gender-dependent risk factors for developing POAG and PACG, respectively, in Pakistan. 23441116 2013