Gene Review:
DYX1C1 - dyslexia susceptibility 1 candidate 1
Homo sapiens
Synonyms:
CILD25, DNAAF4, DYX1, DYXC1, Dyslexia susceptibility 1 candidate gene 1 protein, ...
- A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Taipale, M., Kaminen, N., Nopola-Hemmi, J., Haltia, T., Myllyluoma, B., Lyytinen, H., Muller, K., Kaaranen, M., Lindsberg, P.J., Hannula-Jouppi, K., Kere, J. Proc. Natl. Acad. Sci. U.S.A. (2003)
- Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q. Chapman, N.H., Igo, R.P., Thomson, J.B., Matsushita, M., Brkanac, Z., Holzman, T., Berninger, V.W., Wijsman, E.M., Raskind, W.H. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2004)
- DYX1C1 functions in neuronal migration in developing neocortex. Wang, Y., Paramasivam, M., Thomas, A., Bai, J., Kaminen-Ahola, N., Kere, J., Voskuil, J., Rosen, G.D., Galaburda, A.M., Loturco, J.J. Neuroscience (2006)
- Family-based association study of DYX1C1 variants in autism. Ylisaukko-Oja, T., Peyrard-Janvid, M., Lindgren, C.M., Rehnström, K., Vanhala, R., Peltonen, L., Järvelä, I., Kere, J. Eur. J. Hum. Genet. (2005)
- A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia. Marino, C., Giorda, R., Luisa Lorusso, M., Vanzin, L., Salandi, N., Nobile, M., Citterio, A., Beri, S., Crespi, V., Battaglia, M., Molteni, M. Eur. J. Hum. Genet. (2005)
- No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy. Bellini, G., Bravaccio, C., Calamoneri, F., Donatella Cocuzza, M., Fiorillo, P., Gagliano, A., Mazzone, D., del Giudice, E.M., Scuccimarra, G., Militerni, R., Pascotto, A. J. Mol. Neurosci. (2005)
- TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. Meng, H., Hager, K., Held, M., Page, G.P., Olson, R.K., Pennington, B.F., Defries, J.C., Smith, S.D., Gruen, J.R. Hum. Genet. (2005)
- Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Scerri, T.S., Fisher, S.E., Francks, C., MacPhie, I.L., Paracchini, S., Richardson, A.J., Stein, J.F., Monaco, A.P. J. Med. Genet. (2004)
- Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. Threlkeld, S.W., McClure, M.M., Bai, J., Wang, Y., Loturco, J.J., Rosen, G.D., Fitch, R.H. Brain Res. Bull. (2007)