# CBGDA: a manually curated resource for gene–disease associations based on genome-wide CRISPR

**Authors:** Qingsong Du, Zhiyu Zhang, Wanyi Yang, Xunyu Zhou, Nan Zhou, Chuanfang Wu, Jinku Bao

PMC · DOI: 10.1093/database/baae077 · Database: The Journal of Biological Databases and Curation · 2024-08-30

## TL;DR

CBGDA is a new database that curates gene-disease associations from CRISPR screening to help researchers understand how genes contribute to diseases.

## Contribution

CBGDA is the first manually curated database focusing on gene-disease associations derived from genome-wide CRISPR screening.

## Key findings

- CBGDA includes over 200 manually curated gene-disease associations from CRISPR screening studies.
- The database integrates data from other resources to provide a comprehensive view of gene-disease relationships.
- CBGDA offers insights into gene expression patterns, chemical data, and genetic variants in diseases.

## Abstract

The field of understanding the association between genes and diseases is rapidly expanding, making it challenging for researchers to keep up with the influx of new publications and genetic datasets. Fortunately, there are now several regularly updated databases available that focus on cataloging gene–disease relationships. The development of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas9 system has revolutionized the field of gene editing, providing a highly efficient, accurate, and reliable method for exploring gene–disease associations. However, currently, there is no resource specifically dedicated to collecting and integrating the latest experimentally supported gene–disease association data derived from genome-wide CRISPR screening. To address this gap, we have developed the CRISPR-Based Gene–Disease Associations (CBGDA) database, which includes over 200 manually curated gene–disease association data derived from genome-wide CRISPR screening studies. Through CBGDA, users can explore gene–disease association data derived from genome-wide CRISPR screening, gaining insights into the expression patterns of genes in different diseases, associated chemical data, and variant information. This provides a novel perspective on understanding the associations between genes and diseases. What is more, CBGDA integrates data from several other databases and resources, enhancing its comprehensiveness and utility. In summary, CBGDA offers a fresh perspective and comprehensive insights into the research on gene–disease associations. It fills the gap by providing a dedicated resource for accessing up-to-date, experimentally supported gene–disease association data derived from genome-wide CRISPR screening.

Database URL: http://cbgda.zhounan.org/main

## Full-text entities

- **Genes:** KAT7 (lysine acetyltransferase 7) [NCBI Gene 11143] {aka HBO1, HBOA, MYST2, ZC2HC7}, MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193] {aka ACTFS, HDMX, LSKB, hdm2}
- **Diseases:** ICD (MESH:D008310), cardiovascular diseases (MESH:D002318), hemophilia (MESH:D006467), cystic fibrosis (MESH:D003550), Inheritance (MESH:D030342), HCC (MESH:D006528), cancer (MESH:D009369), Man (MESH:D016750), Werner syndrome (MESH:D014898), diabetes (MESH:D003920), hereditary breast cancer (MESH:D001943), Disease (MESH:D004194)
- **Chemicals:** phosphorus (MESH:D010758)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11363955/full.md

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Source: https://tomesphere.com/paper/PMC11363955