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DiseaseEnhancer: a resource of human disease-associated enhancer catalog

Large-scale sequencing studies discovered substantial genetic variants occurring in enhancers which regulate genes via long range chromatin interactions. Importantly, such variants could affect enhancer regulation by changing transcription factor bindings or enhancer hijacking, and in turn, make an...

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Autores principales: Zhang, Guanxiong, Shi, Jian, Zhu, Shiwei, Lan, Yujia, Xu, Liwen, Yuan, Huating, Liao, Gaoming, Liu, Xiaoqin, Zhang, Yunpeng, Xiao, Yun, Li, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753380/
https://www.ncbi.nlm.nih.gov/pubmed/29059320
http://dx.doi.org/10.1093/nar/gkx920
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author Zhang, Guanxiong
Shi, Jian
Zhu, Shiwei
Lan, Yujia
Xu, Liwen
Yuan, Huating
Liao, Gaoming
Liu, Xiaoqin
Zhang, Yunpeng
Xiao, Yun
Li, Xia
author_facet Zhang, Guanxiong
Shi, Jian
Zhu, Shiwei
Lan, Yujia
Xu, Liwen
Yuan, Huating
Liao, Gaoming
Liu, Xiaoqin
Zhang, Yunpeng
Xiao, Yun
Li, Xia
author_sort Zhang, Guanxiong
collection PubMed
description Large-scale sequencing studies discovered substantial genetic variants occurring in enhancers which regulate genes via long range chromatin interactions. Importantly, such variants could affect enhancer regulation by changing transcription factor bindings or enhancer hijacking, and in turn, make an essential contribution to disease progression. To facilitate better usage of published data and exploring enhancer deregulation in various human diseases, we created DiseaseEnhancer (http://biocc.hrbmu.edu.cn/DiseaseEnhancer/), a manually curated database for disease-associated enhancers. As of July 2017, DiseaseEnhancer includes 847 disease-associated enhancers in 143 human diseases. Database features include basic enhancer information (i.e. genomic location and target genes); disease types; associated variants on the enhancer and their mediated phenotypes (i.e. gain/loss of enhancer and the alterations of transcription factor bindings). We also include a feature on our website to export any query results into a file and download the full database. DiseaseEnhancer provides a promising avenue for researchers to facilitate the understanding of enhancer deregulation in disease pathogenesis, and identify new biomarkers for disease diagnosis and therapy.
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spelling pubmed-57533802018-01-05 DiseaseEnhancer: a resource of human disease-associated enhancer catalog Zhang, Guanxiong Shi, Jian Zhu, Shiwei Lan, Yujia Xu, Liwen Yuan, Huating Liao, Gaoming Liu, Xiaoqin Zhang, Yunpeng Xiao, Yun Li, Xia Nucleic Acids Res Database Issue Large-scale sequencing studies discovered substantial genetic variants occurring in enhancers which regulate genes via long range chromatin interactions. Importantly, such variants could affect enhancer regulation by changing transcription factor bindings or enhancer hijacking, and in turn, make an essential contribution to disease progression. To facilitate better usage of published data and exploring enhancer deregulation in various human diseases, we created DiseaseEnhancer (http://biocc.hrbmu.edu.cn/DiseaseEnhancer/), a manually curated database for disease-associated enhancers. As of July 2017, DiseaseEnhancer includes 847 disease-associated enhancers in 143 human diseases. Database features include basic enhancer information (i.e. genomic location and target genes); disease types; associated variants on the enhancer and their mediated phenotypes (i.e. gain/loss of enhancer and the alterations of transcription factor bindings). We also include a feature on our website to export any query results into a file and download the full database. DiseaseEnhancer provides a promising avenue for researchers to facilitate the understanding of enhancer deregulation in disease pathogenesis, and identify new biomarkers for disease diagnosis and therapy. Oxford University Press 2018-01-04 2017-10-20 /pmc/articles/PMC5753380/ /pubmed/29059320 http://dx.doi.org/10.1093/nar/gkx920 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Database Issue
Zhang, Guanxiong
Shi, Jian
Zhu, Shiwei
Lan, Yujia
Xu, Liwen
Yuan, Huating
Liao, Gaoming
Liu, Xiaoqin
Zhang, Yunpeng
Xiao, Yun
Li, Xia
DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title_full DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title_fullStr DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title_full_unstemmed DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title_short DiseaseEnhancer: a resource of human disease-associated enhancer catalog
title_sort diseaseenhancer: a resource of human disease-associated enhancer catalog
topic Database Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753380/
https://www.ncbi.nlm.nih.gov/pubmed/29059320
http://dx.doi.org/10.1093/nar/gkx920
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