AGEX - Alagille Genetics Exploration Database



About AGEX database
The Alagille Database is a curated collection of genetic mutations in the JAG1 and NOTCH2 genes, associated with Alagille syndrome, a rare pediatric liver disorder with systemic complications. It compiles data from scientific literature, clinical reports, and unpublished cases, providing detailed information on mutation types, their effects on JAG1 and NOTCH2 proteins, and pathogenicity predictions based on computational analyses. The database serves as a centralized repository of genetic and molecular information related to Alagille syndrome.


User Manual
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Terms of Use

Data Usage: All data available in AGEX can be used for academic and non-commercial research purposes only.

Citation:
Kindly cite us as AGEX: A Comprehensive Database of Clinically Relevant Genetic Variants Associated with Alagille Syndrome

Disclaimer: AGEX is a database for Alagille Syndrome designed to provide comprehensive genetic and clinical information on the disease. However, the information provided in AGEX is not intended to replace medical advice or treatment from a qualified healthcare professional. Users should exercise their own discretion in interpreting and using the data.