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

FESD: a Functional Element SNPs Database in human.

Nucleic acids research - 1 Jan 2005

Kang Hyo Jin, Choi Kyoung Oak, Kim Byung-Dong, Kim Sangsoo, Kim Young Joo

Abstract excerpt

We have created the Functional Element SNPs Database (FESD) that categorizes functional elements in human genic regions and provides a set of single nucleotide polymorphisms (SNPs) located within each area. In the FESD, the human genic regions were divided into 10 different functional elements, such as promoter regions, CpG islands, 5'-untranslated regions (5'-UTRs), translation start sites, splice sites, coding...

Read the complete abstract on PubMed

Topics

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

Share to Genome, Human
Share to Haplotypes
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Databases, Nucleic Acid

Share to Gene Components

Share to Polymorphism, Single Nucleotide

Share to User-Computer Interface

Source

Open in PubMed Open full text

Identifiers

PMID: 15608252
DOI: 10.1093/nar/gki082
PMCID: PMC540036

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FESD: a Functional Element SNPs Database in human.PMID 15608252Read ↗

VARAdb: a comprehensive variation annotation database for human.Semantic proximity Read ↗

rSNPBase 3.0: an updated database of SNP-related regulatory elements, element-gene pairs and SNP-based gene regulatory networks.Semantic proximity Read ↗

An integrated encyclopedia of DNA elements in the human genome.Semantic proximity Read ↗

SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions.Semantic proximity Read ↗

A brief review on the Human Encyclopedia of DNA Elements (ENCODE) project.Semantic proximity Read ↗

Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.Semantic proximity Read ↗

rVarBase: an updated database for regulatory features of human variants.Semantic proximity Read ↗

Functional analysis of novel SNPs and mutations in human and mouse genomes.Semantic proximity Read ↗

ssSNPTarget: genome-wide splice-site Single Nucleotide Polymorphism database.Semantic proximity Read ↗

Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequencesSemantic proximity Read ↗

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

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.Semantic proximity Read ↗

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