Analysis of SYNJ1, a candidate gene for 21q22 linked bipolar disorder: a replication study

Psychiatry Res. 2004 Jun 30;127(1-2):157-61. doi: 10.1016/j.psychres.2004.03.003.

Abstract

Linkage analysis has shown that chromosome 21q22 may contain a candidate gene for bipolar disorder (BPD). One potential 21q22 candidate gene we previously analyzed is SYNJ1, which encodes synaptojanin 1, an inositol 5-phosphatase. Previous mutation screening of SYNJ1 identified three rare functional variants, one of which is a polymorphic variant near the intron 12-oxon 12 border. The rare variants were found only in a total of four BPD patients and no controls, and a trend toward significance was found for the intron 12 polymorphism. In an analysis of a new set of 84 bipolar patients, none of the rare variants were detected. There was an increase in allele 2 for the intron 12 polymorphism, similar to our original study, but the result was not significant. The combined data from both studies continue to show a trend toward significance for allele 2 homozygotes in BPD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Bipolar Disorder / diagnosis
  • Bipolar Disorder / ethnology
  • Bipolar Disorder / genetics*
  • Chromosomes, Human, Pair 21 / genetics*
  • Czech Republic
  • DNA Primers / genetics
  • DNA-Binding Proteins
  • Diagnostic and Statistical Manual of Mental Disorders
  • Gene Expression / genetics
  • Genetic Linkage / genetics
  • Genotype
  • Humans
  • Introns / genetics
  • Nerve Tissue Proteins / genetics*
  • Phosphoric Monoester Hydrolases / genetics*
  • Point Mutation / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics
  • Replication Protein A
  • Synaptic Vesicles / genetics
  • United States

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Nerve Tissue Proteins
  • RPA1 protein, human
  • Replication Protein A
  • synaptojanin
  • Phosphoric Monoester Hydrolases