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

RMVar: an updated database of functional variants involved in RNA modifications.

Nucleic acids research - 8 Jan 2021

Luo Xiaotong, Li Huiqin, Liang Jiaqi, Zhao Qi, Xie Yubin, Ren Jian, Zuo Zhixiang

Abstract excerpt

Distinguishing the few disease-related variants from a massive number of passenger variants is a major challenge. Variants affecting RNA modifications that play critical roles in many aspects of RNA metabolism have recently been linked to many human diseases, such as cancers. Evaluating the effect of genetic variants on RNA modifications will provide a new perspective for understanding the pathogenic mechanism of...

Read the complete abstract on PubMed

Topics

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

Share to Alternative Splicing
Share to Computer Graphics
Share to Internet

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Molecular Sequence Annotation

Share to RNA-Binding Proteins

Share to RNA, Circular

Share to RNA, Neoplasm

Share to RNA Processing, Post-Transcriptional

Source

Open in PubMed Open full text

Identifiers

PMID: 33021671
DOI: 10.1093/nar/gkaa811
PMCID: PMC7779057

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

RMVar: an updated database of functional variants involved in RNA modifications.PMID 33021671Read ↗

RMVar 2.0: an updated database of functional variants in RNA modifications.Semantic proximity Read ↗

m6AVar: a database of functional variants involved in m6A modification.Semantic proximity Read ↗

RMDisease: a database of genetic variants that affect RNA modifications, with implications for epitranscriptome pathogenesis.Semantic proximity Read ↗

RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication.Semantic proximity Read ↗

m6ASNP: a tool for annotating genetic variants by m6A function.Semantic proximity Read ↗

RMBase v2.0: deciphering the map of RNA modifications from epitranscriptome sequencing data.Semantic proximity Read ↗

Allele-specific RNA N 6-methyladenosine modifications reveal functional genetic variants in human tissues.Semantic proximity Read ↗

RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins.Semantic proximity Read ↗

m6A Modification in Coding and Non-coding RNAs: Roles and Therapeutic Implications in Cancer.Semantic proximity Read ↗

DirectASRM: uncovering allele-specific post-transcriptional RNA modifications through direct RNA sequencing.Semantic proximity Read ↗

Pharmacoepitranscriptomic landscape revealing m6A modification could be a drug-effect biomarker for cancer treatmentSemantic proximity Read ↗

Classification of miRNA-related sequence variations.Semantic proximity Read ↗

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