Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

FESD

General information

URL: http://combio.kribb.re.kr/ksnp/resd/
Full name: Functional Element SNPs Database
Description: Functional Element SNPs Database (FESD) categorizes functional elements in human genic regions and provides a set of single nucleotide polymorphisms (SNPs) located within each area.
Year founded: 2005
Last update:
Version:
Accessibility:
Unaccessible
Country/Region: Korea, Republic of

Classification & Tag

Data type:
DNA
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: Korea Research Institute of Bioscience and Biotechnology
Address: 52 Eoeun-dong, Yuseong-gu, Daejeon 305-333, Korea
City: Daejeon
Province/State:
Country/Region: Korea, Republic of
Contact name (PI/Team): Young Joo Kim
Contact email (PI/Helpdesk): yjkim@kribb.re.kr

Publications

15608252
FESD: a Functional Element SNPs Database in human. [PMID: 15608252]
Kang HJ, Choi KO, Kim BD, Kim S, Kim YJ.

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 exons, introns, translation stop sites, polyadenylation signals and 3'-UTRs, and subsequently, all the known SNPs were assigned to each functional element at their respective position. With the FESD web interface, users can select a set of SNPs in the specific functional elements and get their flanking sequences for genotyping experiments, which will help in finding mutations that contribute to the common and polygenic diseases. A web interface for the FESD is freely available at http://combio.kribb.re.kr/ksnp/resd/.

Nucleic Acids Res. 2005:33(Database issue) | 22 Citations (from Europe PMC, 2025-12-13)

Ranking

All databases:
5069/6895 (26.497%)
Genotype phenotype and variation:
721/1005 (28.358%)
5069
Total Rank
22
Citations
1.1
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Record metadata

Created on: 2015-07-14
Curated by:
Lin Liu [2022-08-20]
Lina Ma [2018-06-14]
Lina Ma [2016-06-03]
Jian Sang [2016-04-03]