Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE Approximately 1% of normal tension glaucoma (NTG) cases are caused by TANK-binding kinase 1 (TBK1) gene duplications and triplications. 28984711 2017
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE The myocilin (MYOC) and optineurin (OPTN) genes were directly sequenced in 112 unrelated patients, including 17 with primary open‑angle glaucoma, 19 with juvenile open‑angle glaucoma, and 76 with normal tension glaucoma. 27485216 2016
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE Gain-of-function of TBK1 are associated with NTG, whereas loss-of-function mutations result in ALS/FTD or in HSE. 27211305 2016
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.100 GeneticVariation disease GWASCAT Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. 26752265 2016
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 Biomarker disease BEFREE TBK1 inhibition has emerged as a potential therapy for NTG. 27693724 2016
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE In this manuscript, we focus on the OPTN E50K mutation, the most common mutation for NTG, to describe the molecular mechanism of NTG by expressing a mutant Optn gene in cells and genetically modified mice. 27693724 2016
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE Mutations of OPTN are associated with normal tension glaucoma and amyotrophic lateral sclerosis. 26142952 2016
Entrez Id: 90488
Gene Symbol: TMEM263
TMEM263
0.100 GeneticVariation disease GWASCAT Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. 26752265 2016
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE Mutations in two genes, optineurin (OPTN) and TANK binding kinase 1 (TBK1), cause familial NTG and have known roles in the catabolic cellular process autophagy. 27275741 2016
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE Certain missense mutations in optineurin/OPTN and amplification of TBK1 are associated with normal tension glaucoma. 26376340 2015
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE Further, the TBK1 copy number variation segregated with normal-tension glaucoma in the family members of the probands, showing an autosomal dominant pattern of inheritance. 25284765 2015
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE Certain missense mutations in optineurin/OPTN and amplification of TBK1 are associated with normal tension glaucoma. 26376340 2015
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE The gene that causes normal tension glaucoma (NTG) in a large pedigree was recently mapped to a region of chromosome 12q14 (GLC1P) that contains the genes TBK1, XPOT, RASSF3, and GNS. 23421332 2014
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 GeneticVariation disease BEFREE Duplication of the TBK1 gene is a rare cause of NTG. 24699864 2014
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE The optineurin (OPTN) E50K mutation was first identified in familial primary open-angle glaucoma (POAG), the onset of which is not associated with intraocular pressure (IOP) elevation, and is classified as normal-tension glaucoma (NTG). 23669351 2013
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 Biomarker disease BEFREE Mutations in other genes involved in autophagy (TLR4 and OPTN) have been associated with NTG. 23286385 2013
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE Mutations in the optineurin (OPTN) gene have been associated with normal tension glaucoma and with amyotrophic lateral sclerosis (ALS). 23062601 2013
Entrez Id: 4976
Gene Symbol: OPA1
OPA1
0.100 GeneticVariation disease BEFREE We evaluated POAG overall as well as two subtypes of POAG defined as intraocular pressure (IOP) ≥22 mmHg (high-pressure glaucoma [HPG]) or IOP <22 mmHg (normal pressure glaucoma [NPG]) at diagnosis. 23869166 2013
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 Biomarker disease BEFREE TAP showed that NAP1, TANK and TBKBP1 interact with TBK1 and are good candidates for contributing to NTG. 23286385 2013
Entrez Id: 4976
Gene Symbol: OPA1
OPA1
0.100 GeneticVariation disease BEFREE We then subdivided the case groups into two subtypes based on the value of intraocular pressure (IOP)--POAG with high IOP (high pressure glaucoma, HPG) and that with normal IOP (normal pressure glaucoma, NPG)--and performed the GWAS using the two data sets, as the prevalence of NPG in Japanese is much higher than in Caucasians. 22428042 2012
Entrez Id: 4976
Gene Symbol: OPA1
OPA1
0.100 GeneticVariation disease BEFREE In subgroup analyses by ethnicity, we detected an association between both OPA1 polymorphisms and risk for NTG in Caucasians but not in Asians. 22879959 2012
Entrez Id: 29110
Gene Symbol: TBK1
TBK1
0.100 Biomarker disease BEFREE Together, these data link the duplication of genes on chromosome 12q14 with familial NTG and suggest that an extra copy of the encompassed TBK1 gene is likely responsible for these cases of glaucoma. 21447600 2011
Entrez Id: 10133
Gene Symbol: OPTN
OPTN
0.100 GeneticVariation disease BEFREE One of the candidate genes, optineurin, is linked principally to normal tension glaucoma, a subtype of POAG. 20161783 2010
Entrez Id: 4976
Gene Symbol: OPA1
OPA1
0.100 GeneticVariation disease BEFREE Results suggested that genetic variation in five of the candidate genes (RDX, SNX16, OPA1, SOD2 and CYP1B1) is unlikely to confer major risk to develop normal tension glaucoma in the German population. 19754948 2009
Entrez Id: 4976
Gene Symbol: OPA1
OPA1
0.100 Biomarker disease BEFREE OPA1 association with POAG may be limited to patients with normal tension glaucoma in these populations. 18079692 2007