Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations

T. Ohtsuki, Y. Horiuchi, M. Koga, H. Ishiguro, T. Inada, N. Iwata, N. Ozaki, H. Ujike, Y. Watanabe, T. Someya, T. Arinami

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Chromosome 1p13 is linked with schizophrenia in Japanese families, and one of the candidate genes in this region is the netrin G1 (NTNG1) gene at 1p13.3. Associations of 56 tag single-nucleotide polymorphisms (SNPs) with schizophrenia were explored by transmission disequilibrium analysis in 160 Japanese trios and by case-control analysis in 2174 Japanese cases and 2054 Japanese controls. An association between SNP rs628117 and schizophrenia was identified by case-control comparison (nominal allelic p = 0.0009; corrected p = 0.006). The associated polymorphism is located in intron 9 and in the haplotype block encompassing the alternatively spliced exons of the gene. Allelic association of a different SNP in the same haplotype block in Japanese families was previously reported. These findings support that the NTNG1 gene is associated with schizophrenia in the Japanese.

Original languageEnglish
Pages (from-to)194-197
Number of pages4
JournalNeuroscience Letters
Volume435
Issue number3
DOIs
Publication statusPublished - 25-04-2008

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)

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