FABP7 maps onto human chromosome 6q22.31, a schizophrenia
linkage region corroborated by a meta-analysis. As of 2008, two studies have been conducted into FABP7 as a possible risk gene for
schizophrenia, with one, that tested for only one SNP, showing negative and another, with seven SNPs, a positive result. The effect of the gene in the latter study was stronger in males. This study also linked FABP7 variation to weak
prepulse inhibition in mice; deficit in PPI is an
endophenotypic trait observed in schizophrenia patients and their relatives. == References ==