Functional implications of a psychiatric risk variant within CACNA1C in induced human neurons.
Ontology highlight
ABSTRACT: Psychiatric disorders have clear heritable risk. Several large-scale genome-wide association studies have revealed a strong association between susceptibility for psychiatric disorders, including bipolar disease, schizophrenia and major depression, and a haplotype located in an intronic region of the L-type voltage-gated calcium channel (VGCC) subunit gene CACNA1C (peak associated SNP rs1006737), making it one of the most replicable and consistent associations in psychiatric genetics. In the current study, we used induced human neurons to reveal a functional phenotype associated with this psychiatric risk variant. We generated induced human neurons, or iN cells, from more than 20 individuals harboring homozygous risk genotypes, heterozygous or homozygous non-risk genotypes at the rs1006737
SUBMITTER: Yoshimizu T
PROVIDER: S-EPMC4394050 | biostudies-literature | 2015 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA