Accession |
PRJCA002978 |
Title |
UVEOGENE |
Relevance |
Medical |
Data types |
Variation
|
Organisms |
Homo sapiens
|
Description |
Uveitis is an intraocular inflammatory disease which can lead to serious visual impairment. To discover the exact genetic background of uveitis, we developed an SNP database specific for uveitis, UVEOGENE, which includes 370 genes and 918 SNPs covering 14 uveitis entities and 40 populations from 286 PubMed English language papers. Stratification analyses by gender, HLA status, and different clinical features were also extracted from the publications. As a result, 371 associations were judged as statistically significant. These associations were also shared with Global Variome shared Leiden Open Variation Database (LOVD)(https://databases.lovd.nl/shared/genes). Based on these associations, we investigated the genetic relationship among three widely studied uveitis entities including Behcet's disease (BD), Vogt Koyanagi Harada (VKH) disease, and acute anterior uveitis (AAU). Furthermore, UVEOGENE can be used as a reliable and informative resource to identify similarities as well as differences in the genetic susceptibility among uveitis and other autoimmune diseases. UVEOGENE is freely accessible at http://www.uvogene.com. |
Sample scope |
Blood |
Release date |
2020-07-06 |
Publication |
PubMed ID |
Article title |
Journal name |
DOI |
Year |
30614601
|
UVEOGENE: An SNP Database for Investigations on Genetic Factors Associated With Uveitis and Their Relationship With Other Systemic Autoimmune Diseases
|
Human mutation
|
10.1002/humu.23702
|
2019
|
|
Data provider |
|
Biomaterial provider |
Peizeng Yang |
Grants |
Agency |
program |
Grant ID |
Grant title |
Ministry of Science and Technology of the People's Republic of China (MOST)
|
National Key Technologies R&D Program
|
2016YFC0904000
|
|
|
External link |
|
Submitter |
Peizeng
Yang (peizengycmu@126.com)
|
Organization |
The First Affiliated Hospital of Chongqing Medical University |
Submission date |
2020-07-06 |