Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions.

Human mutation - 1 Jun 2020

Li Chang, Mou Chengcheng, Swartz Michael D, Yu Bing, Bai Yongsheng, Tu Yicheng, Liu Xiaoming

Abstract excerpt

MicroRNAs (miRNA) are short noncoding RNAs that can repress the expression of protein-coding messenger RNAs (mRNAs) by binding to the 3'-untranslated region (UTR) of the target. Genetic mutations such as single nucleotide variants (SNVs) in the 3'-UTR of the mRNAs can disrupt miRNA regulation. In this study, we presented dbMTS, a database for miRNA target site (MTS) SNVs and their functional annotations. This...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 3' Untranslated Regions
Share to Computational Biology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Databases, Genetic

Share to Internet

Share to MicroRNAs

Share to Polymorphism, Single Nucleotide

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 32227657
DOI: 10.1002/humu.24020
PMCID: PMC7251985

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions.PMID 32227657Read ↗

dbMTS: a comprehensive database of putative human microRNA target site SNVs and their functional predictionsSemantic proximity Read ↗

miRNASNP-v3: a comprehensive database for SNPs and disease-related variations in miRNAs and miRNA targets.Semantic proximity Read ↗

MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants.Semantic proximity Read ↗

Identification of MicroRNA-Related Tumorigenesis Variants and Genes in the Cancer Genome Atlas (TCGA) Data.Semantic proximity Read ↗

miRdSNP: a database of disease-associated SNPs and microRNA target sites on 3'UTRs of human genes.Semantic proximity Read ↗

MSDD: a manually curated database of experimentally supported associations among miRNAs, SNPs and human diseases.Semantic proximity Read ↗

A review of databases predicting the effects of SNPs in miRNA genes or miRNA-binding sites.Semantic proximity Read ↗

Human polymorphism at microRNAs and microRNA target sites.Semantic proximity Read ↗

Changes in miRNA secondary structure can predict mutations associated with cancer and other diseasesSemantic proximity Read ↗

Updated review of advances in microRNAs and complex diseases: experimental results, databases, webservers and data fusion.Semantic proximity Read ↗

Functional and evolutionary significance of human microRNA seed region mutations.Semantic proximity Read ↗

MicroRNAs and complex diseases: from experimental results to computational models.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.