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Localization of the Catf1 transcription factor gene to mouse Chromosome 19

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References

  • Carrier, L., Hengstenberg, C., Beckmann, J.S., Guicheney, P., Dufour, C., Bercovici, J., Dausse, E., Berebbi-Bertrand, I., Wisnewsky, C., Pulvenis, D., Fetler, L., Vignal, A., Weissenbach, J., Hillaire, D., Feingold, J., Bouhour, J.-B., Hagege, A., Desnos, M., Isnard, R., Dubourg, O., Komajda, M., Schwartz, K. (1993). Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature Genet. 4, 311–313.

    Google Scholar 

  • Cookson, W.O.C.M., Sharp, P.A., Faux, J.A., Hopkin, J.M. (1989). Linkage between immunoglobulin E responses underlying asthma and rhinitis and chromosome 11q. Lancet, I, 1292–1294.

    Google Scholar 

  • Copeland, N.G., Jenkins, N.A., Gilbert, D.J., Eppig, J.T., Maltais, L.J., Miller, J.C., Dietrich, W.F., Weaver, A., Lincoln, S.E., Steen, R.G., Stein, L.D., Nadeau, J.H., Lander, E.S. (1993). A genetic linkage map of the mouse: current applications and future prospects. Science, 262, 57–66.

    Google Scholar 

  • Deol, M.S., Lane, P.W. (1966). A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse. J. Embryol. Exp. Morphol., 16, 543–558.

    Google Scholar 

  • Dietrich, W., Katz, H., Lincoln, S.E., Shin, H.S., Friedman, J., Dracopoli, N.C., Lander, E.S. (1992). A genetic map of the mouse suitable for typing intraspecific crosses. Genetics, 131, 423–447.

    Google Scholar 

  • Dietrich, W., Miller, J.C., Steen, R.G., Merchant, M., Damron, D., Nahf, R., Gross, A., Joyce, D.C., Wessel, M., Dredge, R.D., Marquis, A., Stein, L.D., Goodman, N., Page, D.C., Lander, E.S. (1994). A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nature Genet. 7, 220–245.

    Google Scholar 

  • Fukita, Y., Mizuta, T., Shirozu, M., Ozawa, K., Shimuzu, A., Honjo, T. (1993). The human Sμbp2, a DNA-binding protein specific to the singlestranded guanine-rich sequence related to the immunoglobulin μ chain switch region. J. Biol. Chem., 268, 17463–17470.

    Google Scholar 

  • Janson, M., Larsson, C., Werelius, B., Jones, C., Glaser, T., Nakamura, Y., Jones, C.J., Nordenskjöld, M. (1991). Detailed physical map of human chromosomal region 11q12–13 shows high meiotic recombination rate around the MEN1 locus. Proc. Natl. Acad. Sci. USA 88, 10609–10613.

    Google Scholar 

  • Kullmann, F., Koch, R., Feichtinger, W., Geisen, H., Schmid, M., Grimm, T. (1993). Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy. Klin. Padiat. 205, 185–189.

    Google Scholar 

  • Larsson, C., Weber, G., Kvanta, E., Lewis, K., Janson, M., Jones, C., Glaser, T., Evans, G., Nordenskjöld. (1992). Isolation and mapping of polymorphic cosmic clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus. Hum. Genet., 89, 187–193.

    Google Scholar 

  • Lebo, R.V., Gorin, F., Fletterick, R.J., Kao, F.T., Cheung, M.C., Bruce, B.D., Kan, Y.W. (1984). High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's Syndrome to chromosome 11. Science, 225, 57–59.

    Google Scholar 

  • Malo, D., Schurr, E., Epstein, D.E., Vekemans, M., Skamene, E., Gros, P. (1991). The host resistance locus Bcg is tightly linked to a group of cytoskeleton-associated protein genes that include Villin and Desmin. Genomics 10, 356–364.

    Google Scholar 

  • Malo, D., Vidal, S., Hu, J., Skamene, E., Gros, P. (1993). High resolution linkage map in the vicinity of the host resistance locus Bcg. Genomics 16, 655–663.

    Google Scholar 

  • Manly, K.F. (1993). A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm. Genome, 4, 303–313.

    Google Scholar 

  • Marks, S.C. Jr., Seifert, M.F., Lane, P.W. (1985). Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse. J. Hered. 76, 171–176.

    Google Scholar 

  • McBride, K., Robitaille, L., Tremblay, S., Argentin, S., Nemer, M. (1993). Fosljun repression of cardiac specific transcription is targeted at a tissue-specific cis element. Mol. Cell. Biol., 13, 600–612.

    Google Scholar 

  • Sweet, H.O., Bronson, R.T. (1991). Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J. Hered., 82:140–144.

    Google Scholar 

  • Tanigami, A., Tokino, T., Takita, K., Takiguchi, S., Nakamura, Y. (1992). A 14Mb physical map of the region at chromosome 11q13 harbouring the MEN1 locus and the tumor amplicon region. Genomics 12, 16–20.

    Google Scholar 

  • Withers, D.A., Harvey, R.C., Faust, J.B., Malnyk, O., Carey, K., Meeker, T.C. (1991). Characterization of a candidate bcl-1 gene. Mol. Cell. Biol. 11:4846–4853.

    Google Scholar 

  • Womack, J.E., MacPipe, A., Meier, H. (1980). Muscle deficient, a new mutation in the mouse. J. Hered., 71:68.

    Google Scholar 

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Sebastiani, G., Durocher, D., Gros, P. et al. Localization of the Catf1 transcription factor gene to mouse Chromosome 19. Mammalian Genome 6, 147–148 (1995). https://doi.org/10.1007/BF00303264

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