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Updated: Jun 3, 2026

13:47
Laser Capture Microdissection of Highly Pure Trabecular Meshwork from Mouse Eyes for Gene Expression Analysis
Published on: June 3, 2018
Summary
A new database compiles mutations and SNPs in key genes (MYOC, OPTN, CYP1B1, WDR36) linked to primary open-angle glaucoma (POAG). This resource aids in understanding glaucoma
Area of Science:
- Ophthalmology
- Genetics
- Bioinformatics
Background:
- Glaucoma is a leading cause of optic nerve blindness globally.
- Primary open-angle glaucoma (POAG) is the most common form, affecting millions.
- MYOC, OPTN, CYP1B1, and WDR36 are significant candidate genes for glaucoma.
Purpose of the Study:
- To compile and integrate mutation and SNP data for key glaucoma-associated genes.
- To develop a centralized database for accessing genetic information related to glaucoma.
- To facilitate statistical and clinical analysis of specific mutations and SNPs.
Main Methods:
- Data compilation of mutations and Single Nucleotide Polymorphisms (SNPs) in MYOC, OPTN, CYP1B1, and WDR36.
- Development of a SQL-based database to store genetic and associated study data.
- Making the database accessible online for public use.
Main Results:
- A comprehensive database of mutations and SNPs in MYOC, OPTN, CYP1B1, and WDR36 has been created.
- The database includes statistical and clinical information relevant to specific genetic variations.
- The resource is available online at http:bicmku.in:8081/glaucoma.
Conclusions:
- The developed database serves as a valuable resource for researchers studying glaucoma genetics.
- It enables easier access to critical genetic data for understanding POAG.
- This tool can aid in the statistical and clinical investigation of glaucoma-related mutations and SNPs.
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