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Functional Variant in a Bitter-Taste Receptor (hTAS2R16) Influences Risk of Alcohol Dependence
- Source :
- The American Journal of Human Genetics. 78:103-111
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- A coding single-nucleotide polymorphism (cSNP), K172N, in hTAS2R16, a gene encoding a taste receptor for bitter beta -glucopyranosides, shows significant association with alcohol dependence (P = .00018). This gene is located on chromosome 7q in a region reported elsewhere to exhibit linkage with alcohol dependence. The SNP is located in the putative ligand-binding domain and is associated with an increased sensitivity to many bitter beta -glucopyranosides in the presence of the N172 allele. Individuals with the ancestral allele K172 are at increased risk of alcohol dependence, regardless of ethnicity. However, this risk allele is uncommon in European Americans (minor-allele frequency [MAF] 0.6%), whereas 45% of African Americans carry the allele (MAF 26%), which makes it a much more significant risk factor in the African American population.
- Subjects :
- Linkage disequilibrium
Protein Conformation
Molecular Sequence Data
Biology
Polymorphism, Single Nucleotide
Linkage Disequilibrium
Receptors, G-Protein-Coupled
Taste receptor
Polymorphism (computer science)
Genetics
Humans
SNP
Genetic Predisposition to Disease
Genetics(clinical)
Allele
Risk factor
Genetics (clinical)
Base Sequence
Alcohol dependence
Articles
Sequence Analysis, DNA
Black or African American
Minor allele frequency
Alcoholism
Chromosomes, Human, Pair 7
Subjects
Details
- ISSN :
- 00029297
- Volume :
- 78
- Database :
- OpenAIRE
- Journal :
- The American Journal of Human Genetics
- Accession number :
- edsair.doi.dedup.....bf0205a545c14d6fd8ccbcb4020780bf