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 2.0: an updated database of functional variants in RNA modifications.

Nucleic acids research - 6 Jan 2025

Huang Yuantai, Zhang Luowanyue, Mu Weiping, Zheng Mohan, Bao Xiaoqiong, Li Huiqin, Luo Xiaotong, Ren Jian, Zuo Zhixiang

Abstract excerpt

Evaluating the impact of genetic variants on RNA modifications (RMs) is crucial for identifying disease-associated variants and understanding the pathogenic mechanisms underlying human diseases. Previously, we developed a database called RMVar to catalog variants linked to RNA modifications in humans and mice. Here, we present an updated version RMVar 2.0 (http://rmvar.renlab.cn). In this updated version, we...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Genetic
Share to Databases, Nucleic Acid

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 Processing, Post-Transcriptional

Source

Open in PubMed Open full text

Identifiers

PMID: 39436017
DOI: 10.1093/nar/gkae924
PMCID: PMC11701541

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 2.0: an updated database of functional variants in RNA modifications.PMID 39436017Read ↗

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

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

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

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

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

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

lncRNASNP v3: an updated database for functional variants in long non-coding RNAs.Semantic proximity Read ↗

Genomic variations in non-coding RNAs: Structure, function and regulation.Semantic proximity Read ↗

Evolutionary conservation and expression of human RNA-binding proteins and their role in human genetic disease.Semantic proximity Read ↗

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

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