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    CMYA5 cardiomyopathy associated 5 [ Homo sapiens (human) ]

    Gene ID: 202333, updated on 5-Mar-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    association between CMYA5 gene polymorphisms and schizophrenia was confirmed in Asian population.

    Association between CMYA5 gene polymorphisms and risk of schizophrenia in Uygur population and a meta-analysis.
    Han S, An Z, Luo X, Zhang L, Zhong X, Du W, Yi Q, Shi Y.

    07/13/2019
    meta-analysis did not provide evidence supporting a contribution of CMYA5 rs3828611 and rs4704591 to schizophrenia susceptibility in Asian populations.

    Updated meta-analysis of CMYA5 rs3828611 and rs4704591 with schizophrenia in Asian populations.
    Hoya S, Watanabe Y, Shibuya M, Someya T.

    03/16/2019
    The results showed that MYBPC3 25-bp deletion polymorphism was significantly associated with elevated risk of left ventricular dysfunction (LVD), while TTN 18 bp I/D, TNNT2 5 bp I/D and myospryn K2906N polymorphisms did not show any significant association with LVD.

    Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
    Kumar S, Mishra A, Srivastava A, Bhatt M, Garg N, Agarwal SK, Pande S, Mittal B.

    04/1/2017
    Specific alleles and haplotype in the CMYA5 confer genetic risk for both schizophrenia and major depressive disorder in the Han Chinese population.

    The CMYA5 gene confers risk for both schizophrenia and major depressive disorder in the Han Chinese population.
    Wang Q, He K, Li Z, Chen J, Li W, Wen Z, Shen J, Qiang Y, Ji J, Wang Y, Shi Y.

    05/30/2015
    meta-analysis confirming association of CMYA5 polymorphisms and schizophrenia in East Asian population.

    The cardiomyopathy-associated 5 (CMYA5) gene and risk of schizophrenia: meta-analysis of rs3828611 and rs4704591 in East Asian populations.
    Watanabe Y, Shibuya M, Someya T.

    10/18/2014
    Association of cardiomyopathy-associated 5 (CMYA5) gene of Schizophrenia, is reported.

    An association analysis of the cardiomyopathy-associated 5 (CMYA5) gene with schizophrenia in a Japanese population.
    Furukawa M, Tochigi M, Otowa T, Arinami T, Inada T, Ujike H, Watanabe Y, Iwata N, Itokawa M, Kunugi H, Hashimoto R, Ozaki N, Kakiuchi C, Kasai K, Sasaki T.

    04/26/2014
    In a Han Chinese sample of schizophrenic patients, SNPs within CMYA5 were associated with the disorder.

    Genetic analysis of common variants in the CMYA5 (cardiomyopathy-associated 5) gene with schizophrenia.
    Zhang R, Zhang H, Li M, Li H, Li Y, Valenzuela RK, Su B, Ma J.

    04/26/2014
    CMYA5 is a new potential substrate of Kcna3 in human heart

    CMYA5: a new potential substrate of Kcna3 in human heart.
    Zhang L, Fan H, Lu R, Xin Y, Zhen X, Liu Z.

    09/14/2013
    2 SNPS in CYMA5, rs4704591 & rs10043986, are significantly associated with schizophrenia. Haplotype conditioned analyses indicated that the association signals observed at these two markers are independent.

    GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
    Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS, GROUP investigators, International Schizophrenia Consortium., Free PMC Article

    03/10/2012
    This study demonstrated that the association between CMYA5 and schizophrenia in Han Chinese.

    A common variant of the cardiomyopathy associated 5 gene (CMYA5) is associated with schizophrenia in Chinese population.
    Li M, Luo XJ, Zhang X, Yang ZH, Xiang K, Xiao X, Su B, Zhao YL, Shen Y, Xu Q, Chen XN, Chen JC, Liu XY, Yin LD, Ma XY, Yang SY, Yu J, Diao HB, Shi XD.

    10/15/2011
    Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies.

    Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies.
    Sarparanta J, Blandin G, Charton K, Vihola A, Marchand S, Milic A, Hackman P, Ehler E, Richard I, Udd B., Free PMC Article

    10/23/2010
    Review discusses interactions that suggest myospryn is involved in two seemingly distinct processes, protein kinase A signalling and vesicular trafficking.

    Biology of myospryn: what's known?
    Sarparanta J.

    01/21/2010
    Polymorphism of myospryn is associated with left ventricular hypertrophy, and an association between a Z-disc protein and cardiac adaptation in response to pressure overload.

    Gene polymorphism of myospryn (cardiomyopathy-associated 5) is associated with left ventricular wall thickness in patients with hypertension.
    Nakagami H, Kikuchi Y, Katsuya T, Morishita R, Akasaka H, Saitoh S, Rakugi H, Kaneda Y, Shimamoto K, Ogihara T, Nakagami H, Kikuchi Y, Katsuya T, Morishita R, Akasaka H, Saitoh S, Rakugi H, Kaneda Y, Shimamoto K, Ogihara T.

    01/21/2010
    Observational study of gene-disease association. (HuGE Navigator)

    Gene polymorphism of myospryn (cardiomyopathy-associated 5) is associated with left ventricular wall thickness in patients with hypertension.
    Nakagami H, Kikuchi Y, Katsuya T, Morishita R, Akasaka H, Saitoh S, Rakugi H, Kaneda Y, Shimamoto K, Ogihara T, Nakagami H, Kikuchi Y, Katsuya T, Morishita R, Akasaka H, Saitoh S, Rakugi H, Kaneda Y, Shimamoto K, Ogihara T.

    04/3/2008
    perinuclear localization of the TRIM-like protein myospryn requires its binding partner desmin

    Proper perinuclear localization of the TRIM-like protein myospryn requires its binding partner desmin.
    Kouloumenta A, Mavroidis M, Capetanaki Y.

    01/21/2010
    Functions directly downstream of MEF2A at the costamere in striated muscle potentially playing a role in myofibrillogenesis.

    Myospryn is a direct transcriptional target for MEF2A that encodes a striated muscle, alpha-actinin-interacting, costamere-localized protein.
    Durham JT, Brand OM, Arnold M, Reynolds JG, Muthukumar L, Weiler H, Richardson JA, Naya FJ.

    01/21/2010
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