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

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

Nucleic acids research - 6 Jan 2023

Yang Yanbo, Wang Dongyang, Miao Ya-Ru, Wu Xiaohong, Luo Haohui, Cao Wen, Yang Wenqian, Yang Jianye, Guo An-Yuan, Gong Jing

Abstract excerpt

Long non-coding RNAs (lncRNAs) act as versatile regulators of many biological processes and play vital roles in various diseases. lncRNASNP is dedicated to providing a comprehensive repository of single nucleotide polymorphisms (SNPs) and somatic mutations in lncRNAs and their impacts on lncRNA structure and function. Since the last release in 2018, there has been a huge increase in the number of variants and...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Nucleic Acid
Share to MicroRNAs

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to RNA, Long Noncoding

Source

Open in PubMed Open full text

Identifiers

PMID: 36350671
DOI: 10.1093/nar/gkac981
PMCID: PMC9825536

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

lncRNASNP v3: an updated database for functional variants in long non-coding RNAs.PMID 36350671Read ↗

lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs.Semantic proximity Read ↗

LncRBase V.2: an updated resource for multispecies lncRNAs and ClinicLSNP hosting genetic variants in lncRNAs for cancer patients.Semantic proximity Read ↗

Genetic variations associated with long noncoding RNAs.Semantic proximity Read ↗

LincSNP 3.0: an updated database for linking functional variants to human long non-coding RNAs, circular RNAs and their regulatory elements.Semantic proximity Read ↗

NONCODEV5: a comprehensive annotation database for long non-coding RNAs.Semantic proximity Read ↗

LncVar: a database of genetic variation associated with long non-coding genes.Semantic proximity Read ↗

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

miRNASNP-v4: a comprehensive database for miRNA-related SNPs across 17 species.Semantic proximity Read ↗

lncRNAKB: A comprehensive knowledgebase of long non-coding RNAsSemantic proximity Read ↗

Lnc2Cancer 3.0: an updated resource for experimentally supported lncRNA/circRNA cancer associations and web tools based on RNA-seq and scRNA-seq data.Semantic proximity Read ↗

LincSNP 2.0: an updated database for linking disease-associated SNPs to human long non-coding RNAs and their TFBSs.Semantic proximity Read ↗

NCAD v1.0: a database for non-coding variant annotation and interpretation.Semantic proximity Read ↗

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