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    CACNA1C calcium voltage-gated channel subunit alpha1 C [ Homo sapiens (human) ]

    Gene ID: 775, updated on 27-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    NRN1 epistasis with BDNF and CACNA1C: mediation effects on symptom severity through neuroanatomical changes in schizophrenia.

    NRN1 epistasis with BDNF and CACNA1C: mediation effects on symptom severity through neuroanatomical changes in schizophrenia.
    Almodóvar-Payá C, Guardiola-Ripoll M, Giralt-López M, Oscoz-Irurozqui M, Canales-Rodríguez EJ, Madre M, Soler-Vidal J, Ramiro N, Callado LF, Arias B, Gallego C, Pomarol-Clotet E, Fatjó-Vilas M., Free PMC Article

    10/7/2024
    [CACNA1C rs58619945 genotype influences the cortical thickness of attention network among patients with Bipolar disorder].

    [CACNA1C rs58619945 genotype influences the cortical thickness of attention network among patients with Bipolar Ⅰ disorder].
    Zhang X, Liang X, Cheng X, Chen J, Deng W, Zhang Y, Cui L, Cheng X, Li X, Yang C, Ye B, Cao L.

    09/3/2024
    Effects of CACNA1C and ANK3 on cognitive function in patients with bipolar disorder.

    Effects of CACNA1C and ANK3 on cognitive function in patients with bipolar disorder.
    Yang Y, Zhu Z, Hui L, Sun P.

    06/5/2024
    Structural basis for human Cav1.2 inhibition by multiple drugs and the neurotoxin calciseptine.

    Structural basis for human Ca(v)1.2 inhibition by multiple drugs and the neurotoxin calciseptine.
    Gao S, Yao X, Chen J, Huang G, Fan X, Xue L, Li Z, Wu T, Zheng Y, Huang J, Jin X, Wang Y, Wang Z, Yu Y, Liu L, Pan X, Song C, Yan N.

    11/27/2023
    Effect of rs1108580 of DBH and rs1006737 of CACNA1C on Cognition and Tardive Dyskinesia in a North Indian Schizophrenia Cohort.

    Effect of rs1108580 of DBH and rs1006737 of CACNA1C on Cognition and Tardive Dyskinesia in a North Indian Schizophrenia Cohort.
    Punchaichira TJ, Kukshal P, Bhatia T, Deshpande SN, Thelma BK.

    11/22/2023
    The rs216009 single-nucleotide polymorphism of the CACNA1C gene is associated with phantom tooth pain.

    The rs216009 single-nucleotide polymorphism of the CACNA1C gene is associated with phantom tooth pain.
    Morii M, Ohka S, Nishizawa D, Hasegawa J, Nakayama K, Ebata Y, Soeda M, Fukuda KI, Yoshida K, Koshika K, Ichinohe T, Ikeda K., Free PMC Article

    11/3/2023
    A novel risk variant block across introns 36-45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study.

    A novel risk variant block across introns 36-45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study.
    Guo X, Wang S, Lin X, Wang Z, Dou Y, Cao Y, Zhang Y, Luo X, Kang L, Yu T, Wang Z, Tan Y, Gao S, Zheng H, Zhao F, Wang H, Wang K, Xie F, Chen W, Luo X., Free PMC Article

    09/19/2023
    CACNA1C-Related Channelopathies.

    CACNA1C-Related Channelopathies.
    Herold KG, Hussey JW, Dick IE., Free PMC Article

    08/2/2023
    EMC chaperone-CaV structure reveals an ion channel assembly intermediate.

    EMC chaperone-Ca(V) structure reveals an ion channel assembly intermediate.
    Chen Z, Mondal A, Abderemane-Ali F, Jang S, Niranjan S, Montaño JL, Zaro BW, Minor DL Jr., Free PMC Article

    07/26/2023
    Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant.

    Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant.
    Delinière A, Haddad C, Herrera-Siklódy C, Hermida A, Pruvot E, Bressieux-Degueldre S, Millat G, Janin A, Hermida JS, Asatryan B, Chevalier P.

    06/23/2023
    Impact of ZNF804A rs1344706 or CACNA1C rs1006737 polymorphisms on cognition in patients with severe mental disorders: A systematic review and meta-analysis.

    Impact of ZNF804A rs1344706 or CACNA1C rs1006737 polymorphisms on cognition in patients with severe mental disorders: A systematic review and meta-analysis.
    Novaes de Oliveira Roldan AC, Fernandes Júnior LCC, de Oliveira CEC, Nunes SOV.

    03/13/2023
    BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity.

    BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity.
    Bastos CR, Xavier J, Camerini L, Dewes SS, Moreira FP, Wiener CD, Jansen K, Kaster MP, de Mattos Souza LD, da Silva RA, Oses JP, Portela LV, Lara DR, Tovo-Rodrigues L, Ghisleni G.

    01/14/2023
    A CACNA1C variant associated with cardiac arrhythmias provides mechanistic insights in the calmodulation of L-type Ca[2+] channels.

    A CACNA1C variant associated with cardiac arrhythmias provides mechanistic insights in the calmodulation of L-type Ca(2+) channels.
    Zhao J, Segura E, Marsolais M, Parent L., Free PMC Article

    01/11/2023
    A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder.

    A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder.
    Levy RJ, Timothy KW, Underwood JFG, Hall J, Bernstein JA, Pașca SP.

    01/7/2023
    Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

    Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.
    Refisch A, Komatsuzaki S, Ungelenk M, Schumann A, Chung HY, Schilling SS, Jantzen W, Schröder S, Nöthen MM, Mühleisen TW, Hübner CA, Bär KJ., Free PMC Article

    12/3/2022
    Inhibition of L-type voltage-gated calcium channel-mediated Ca(2+) influx suppresses the collective migration and invasion of ameloblastoma.

    Inhibition of L-type voltage-gated calcium channel-mediated Ca(2+) influx suppresses the collective migration and invasion of ameloblastoma.
    Li S, Kim HY, Lee DJ, Park SH, Otsu K, Harada H, Jung YS, Jung HS., Free PMC Article

    11/12/2022
    CACNA1C (CaV1.2) and other L-type calcium channels in the pathophysiology and treatment of psychiatric disorders: Advances from functional genomics and pharmacoepidemiology.

    CACNA1C (Ca(V)1.2) and other L-type calcium channels in the pathophysiology and treatment of psychiatric disorders: Advances from functional genomics and pharmacoepidemiology.
    Harrison PJ, Husain SM, Lee H, Los Angeles A, Colbourne L, Mould A, Hall NAL, Haerty W, Tunbridge EM.

    10/22/2022
    Genetic Polymorphisms in miR-137 and Its Target Genes, TCF4 and CACNA1C, Contribute to the Risk of Bipolar Disorder: A Preliminary Case-Control Study and Bioinformatics Analysis.

    Genetic Polymorphisms in miR-137 and Its Target Genes, TCF4 and CACNA1C, Contribute to the Risk of Bipolar Disorder: A Preliminary Case-Control Study and Bioinformatics Analysis.
    Mokhtari MA, Sargazi S, Saravani R, Heidari Nia M, Mirinejad S, Hadzsiev K, Bene J, Shakiba M., Free PMC Article

    10/15/2022
    A functional neuroimaging association study on the interplay between two schizophrenia genome-wide associated genes (CACNA1C and ZNF804A).

    A functional neuroimaging association study on the interplay between two schizophrenia genome-wide associated genes (CACNA1C and ZNF804A).
    Guardiola-Ripoll M, Almodóvar-Payá C, Lubeiro A, Sotero A, Salvador R, Fuentes-Claramonte P, Salgado-Pineda P, Papiol S, Ortiz-Gil J, Gomar JJ, Guerrero-Pedraza A, Sarró S, Maristany T, Molina V, Pomarol-Clotet E, Fatjó-Vilas M.

    10/8/2022
    Further evidence and meta-analysis support association of a single nucleotide polymorphism rs4765905 in CACNA1C with schizophrenia.

    Further evidence and meta-analysis support association of a single nucleotide polymorphism rs4765905 in CACNA1C with schizophrenia.
    Wang Z, Fu Y, Jiang F, Chen L, Chen W, Guo X, Luo X.

    08/27/2022
    Novel CACNA1C R511Q mutation, located in domain - linker, causes non-syndromic type-8 long QT syndrome.

    Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome.
    Nakajima T, Kawabata-Iwakawa R, Tamura S, Hasegawa H, Kobari T, Itoh H, Horie M, Nishiyama M, Kurabayashi M, Kaneko Y, Ishii H., Free PMC Article

    07/30/2022
    Association between CACNA1C gene rs100737 polymorphism and glutamatergic neurometabolites in bipolar disorder.

    Association between CACNA1C gene rs100737 polymorphism and glutamatergic neurometabolites in bipolar disorder.
    Scotti-Muzzi E, Chile T, Vallada H, Otaduy MCG, Soeiro-de-Souza MG.

    06/18/2022
    Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing.

    Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing.
    Novelli V, Memmi M, Malovini A, Mazzanti A, Liu N, Yanfei R, Bongianino R, Denegri M, Monteforte N, Bloise R, Morini M, Napolitano C.

    05/7/2022
    An independent, replicable, functional and significant risk variant block at intron 3 of CACNA1C for schizophrenia.

    An independent, replicable, functional and significant risk variant block at intron 3 of CACNA1C for schizophrenia.
    Wang Z, Chen W, Cao Y, Dou Y, Fu Y, Zhang Y, Luo X, Kang L, Liu N, Shi YS, Li CR, Xu Y, Guo X, Luo X.

    04/30/2022
    Increased Ca2+ influx through CaV1.2 drives aortic valve calcification.

    Increased Ca2+ influx through CaV1.2 drives aortic valve calcification.
    Matsui M, Bouchareb R, Storto M, Hussain Y, Gregg A, Marx SO, Pitt GS., Free PMC Article

    04/16/2022
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