VIP Variant in ADH1A
Note: The ADH1A gene is found on the minus chromosomal strand. Please note that for standardization, the PharmGKB presents all allele base pairs on the positive chromosomal strand, therefore the alleles within our variant annotations will differ (in a complementary manner) from those in this VIP summary that are given on the minus strand as reported in the literature.
ADH1A has not been as well studied as its isozymes ADH1B and ADH1C, and it is also not the primary alcohol dehydrogenase expressed in adult tissues. Very recent studies using a new statistical test called Diplotype Trend Regression (DTR) have identified potential variants of interest [Articles:16685648, 17185388]. ADH1A is part of a larger gene cluster on chromosome 4 which also includes ADH7, ADH1C, ADH1B, ADH6, ADH4, and ADH3 [Article:16685648]. DTR was applied to this gene cluster using several marker SNPs to detect associations with alcohol dependence and drug dependence [Articles:16685648, 17185388].
ADH1A^SNP11 was one of three markers near ADH1A that were used in the analysis [Article:16685648]. This SNP is located in intron 7 of ADH1A, and is likely functionally inconsequential [Article:16685648]. Still, ADH1A^SNP11 was the only SNP examined in ADH1A that showed a tendency towards an association with alcohol dependence in the African American sample [Article:16685648]. This may indicate that ADH1A^SNP11 is in close proximity to a risk allele that may be in linkage disequilibrium with it [Article:16685648].
| Key Publications: | |
|---|---|
| Drugs / Other Molecules |
Drug (1)
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| Diseases | Alcoholism |
Appendix
| Genomic Variant & GenBank ID: | 24749459 G>C on NT_016354 |
|---|---|
| GoldenPath Position: | chr4:100420762,] (hg18) |
There are several important diplotypes for ADH1A:
ADH1A is part of a gene cluster of alcohol dehydrogenase enzymes on chromosome 4 [Article:16685648]. Some haplotype blocks extend across multiple genes in this region [Article:16685648]. Two recent studies have examined the potential association of diplotypes of ADH1A and other genes in the alcohol dehydrogenase gene cluster on alcohol dependence (AD) [Article:16685648] and Drug Dependence (DD) [Article:17185388]. For the purposes of their article, the authors defined DD as being either cocaine or opioid dependence. The authors used a relatively new statistical technique called diplotype trend regression (DTR) which has many advantages over other commonly used statistical tests [Articles:16685648, 17185388].
A diplotype is basically a genotype that consists of two haplotypes. In the case of ADH1A, the authors genotyped for three marker positions [Articles:16685648, 17185388], and therefore each diplotype consisted of six bases, three on one chromosome, and three on the other. Of the three markers that the authors used to genotype for ADH1A, only ADH1A^SNP11 was located in an intron or exon; the other two markers were flanking the gene, with one upstream, and one downstream [Articles:16685648, 17185388]. The authors found several diplotype combinations that were associated with increased risk for alcohol dependence in their European American sample (AGA/TGA, AGA/TCG, AGA/AGA, TCG/TGA, AGA/TGG, TGA/TGA, TCG/TGG, TGA/TGG, TCG/TCG) [Article:16685648]. Interestingly, two diplotype pairs in the African American sample were found to be protective against alcohol dependence (TCG/TCG, TGA/TGA) [Article:16685648]. This finding is likely explained by the fact that the authors also discovered that ADH1A was found in different LD blocks in the European American and the African American populations [Article:16685648]. In a later study, the authors found similar results when they applied DTR to associate the ADH markers with DD [Article:17185388].
Publications related to rs975833 at chr4:100201739: 2
| Multiple ADH genes modulate risk for drug dependence in both African- and European-Americans. Human molecular genetics. 2007. Luo Xingguang, et al. [Article:17185388@PubMed] | |
| Diplotype trend regression analysis of the ADH gene cluster and the ALDH2 gene: multiple significant associations with alcohol dependence. American journal of human genetics. 2006. Luo Xingguang, et al. [Article:16685648@PubMed] |
Cross-References
- UCSC Golden Path:
- chr4:100201739
- dbSNP:
- rs975833
- ALFRED:
- SI001271L
- HapMap:
- rs975833
Platform Availability
- Illumina
