
pmid: 15261714
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.
Bipolar Disorder, Polymorphism, Genetic, Genotype, Chromosomes, Human, Pair 21, Genetic Linkage, Gene Expression, Nerve Tissue Proteins, Polymerase Chain Reaction, Introns, Phosphoric Monoester Hydrolases, United States, DNA-Binding Proteins, Diagnostic and Statistical Manual of Mental Disorders, Replication Protein A, Humans, Point Mutation, Synaptic Vesicles, Alleles, Czech Republic, DNA Primers
Bipolar Disorder, Polymorphism, Genetic, Genotype, Chromosomes, Human, Pair 21, Genetic Linkage, Gene Expression, Nerve Tissue Proteins, Polymerase Chain Reaction, Introns, Phosphoric Monoester Hydrolases, United States, DNA-Binding Proteins, Diagnostic and Statistical Manual of Mental Disorders, Replication Protein A, Humans, Point Mutation, Synaptic Vesicles, Alleles, Czech Republic, DNA Primers
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