Diverse polymorphism within a short coding region of the human aldehyde dehydrogenase-5 (ALDH5) gene.

Article Details

Citation

Sherman D, Dave V, Hsu LC, Peters TJ, Yoshida A

Diverse polymorphism within a short coding region of the human aldehyde dehydrogenase-5 (ALDH5) gene.

Hum Genet. 1993 Nov;92(5):477-80.

PubMed ID
8244338 [ View in PubMed
]
Abstract

Human aldehyde dehydrogenase-5 gene (originally named as ALDHX) is expressed in liver and testis. The ALDH5 does not contain introns in the coding sequence for 517 amino acid residues. Within a short nucleotide region of the gene, the following three nucleotide changes were found in high frequencies, i.e., a silent C<-->T at nucleotide (nt) 183, C<-->T at nt 257 associated with a Val<-->Ala substitution, and T<-->G at nt 320 associated with a Arg<-->Leu substitution. The frequency of C at nt 183 is 81% in Caucasians and 65% in Japanese, and the difference is statistically not significant. The frequency of C at nt 257 is 76% in Caucasians and 55% in Japanese, and the difference is statistically significant (P = 0.02). The frequency of T at nt 320 is 71% in Caucasians, while it is only 27% in Japanese. The racial difference at nt 320 is highly significant (P < 0.001). No significant difference was found in the genotypes of the three nucleotide positions between alcoholic and nonalcoholic Caucasians within the limited numbers of subjects examined.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Aldehyde dehydrogenase X, mitochondrialP30837Details