Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE The discovery that voltage-gated calcium channel genes such as CACNA1C are part of the aetiology of psychiatric disorders has rekindled interest in the therapeutic potential of L-type calcium channel (LTCC) antagonists. 30755265 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Genetic variation in CACNA1C, which encodes the alpha-1 subunit of Cav1.2 L-type voltage-gated calcium channels (VGCCs), has been strongly linked to risk for psychiatric disorders including schizophrenia and bipolar disorder. 30304534 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE The risk gene CACNA1C is strongly implicated in the etiology of all major psychiatric disorders, such as depressive disorder, bipolar disorder, autism spectrum disorder, and schizophrenia. 30902660 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE In the current study, we use an imaging genetics approach to examine the impact of CACNA1C, one of the most promising genetic risk factors for psychiatric disorders, on prosody processing on a behavioral, functional and microstructural level. 30909026 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE The rs1006737 (A/G) single nucleotide polymorphism within the gene encoding the Ca<sub>v</sub>1.2 subunit of the L-type voltage-dependent calcium channel (CACNA1C) has been strongly implicated in psychiatric disorders. 29733866 2018
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE The CACNA1C locus was previously associated with other psychiatric disorders, but not yet with PTSD. 29362489 2018
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Here we show that embryonic deletion of Cacna1c in forebrain glutamatergic neurons promotes the manifestation of endophenotypes related to psychiatric disorders including cognitive decline, impaired synaptic plasticity, reduced sociability, hyperactivity and increased anxiety. 28696432 2018
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE CACNA1C: Association With Psychiatric Disorders, Behavior, and Neurogenesis. 29982775 2018
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Despite growing evidence of a significant link between CACNA1C and CACNA1D and psychiatric disorders, our understanding of the biological mechanisms by which these LTCCs mediate neuropsychiatric-associated endophenotypes, many of which are shared across the different disorders, remains rudimentary. 28497380 2017
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Seven variants that were earlier associated (genome-wide significantly) with psychiatric disorders at CACNA1C were selected for analyses. 28792954 2017
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Calcium influx through high-voltage-gated Ca2+ channels is central to synaptic plasticity, and altered expression of Cav1.2 channels and the CACNA1C gene have been associated with severe learning deficits and psychiatric disorders. 28604818 2017
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Calcium channel subunits, including CACNA1C, have been associated with multiple psychiatric disorders. 27276213 2016
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Association of CACNA1C and SYNE1 in offspring of patients with psychiatric disorders. 27620326 2016
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Several genome-wide association studies and case-control studies have associated the single nucleotide polymorphism (SNP) rs1006737, situated in CACNA1C encoding the alpha 1C subunit of the L-type voltage-gated calcium channel, with bipolar disorder and other psychiatric disorders. 26541689 2016
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Our study is the first to provide evidence for an impairing behavioral effect of the CACNA1C risk variant rs1006737 on facial emotion recognition in healthy individuals and adds to the growing number of studies pointing towards CACNA1C as affecting intermediate phenotypes of psychiatric disorders. 26611642 2015
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Genome-wide association studies have identified allelic variation in CACNA1C as a risk factor for multiple psychiatric disorders associated with limbic system dysfunction, including bipolar disorder, schizophrenia, and depression. 26401721 2015
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Genome-wide association studies have identified the CACNA1C single nucleotide polymorphism (SNP) rs1006737 as one of the most consistent genetic findings as susceptibility locus for major psychiatric disorders. 24269271 2014
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Our results suggest that CACNA1C plays a role in the development of specific attention deficits in psychiatric disorders by modulation of neural attention networks. 21078228 2011
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Genetic variation in CACNA1C has been repeatedly shown to increase risk for psychiatric disorders, with the strongest evidence for involvement in bipolar disorder. 20638048 2010