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Mouse Chromosome 14

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References

  1. Aitman, T.J., Hearne, C.M., McAleer, M.A., and Todd, J.A.: Mononucleotide repeats are an abundant source of length variants in mouse genomic DNA.Mammalian Genome 1: 206–210, 1991.

    Google Scholar 

  2. Bailey, D.W.: Genetics of histocompatibility in mice. I. New loci and congenic lines.Immunogenetics 2: 249–256, 1975.

    Google Scholar 

  3. Barker, P.E., Royer, H.-D., Ruddle, F.H., and Reinherz, E.L.: Human T cell receptor gene TCRA lies in region 14pter-q21.Cytogenet Cell Genet 40: 576–577, 1985.

    Google Scholar 

  4. Beechey, C.V.: Linkage studies with T(2;14)48H.Mouse Genome 89: 257, 1991.

    Google Scholar 

  5. Beisel, K.W. and Booth, B.J.M.: Identification of three alleles forMus musculus at theMyhc-a locus which co-segregates withNp-2, Tcra, andRib-1 on chromosome 14.Nucleic Acids Res 17: 10519, 1989.

    Google Scholar 

  6. Belin, D., Vassalli, J.-D., Combépine, C., Godeau, F., Nagamine, Y., Reich, E., Kocher, H.P., and Duvoisin, R.M.: Cloning, nucleotide sequencing and expression of cDNAs encoding mouse urokinase-type plasminogen activator.Eur J Biochem 148: 225–232, 1985.

    Google Scholar 

  7. Berman, J.W., Rocha, A.J.D., and Basch, R.: Restriction length polymorphism in the variable region of theTcr locus linked to histocompatibility antigenH-8 on murine chromosome 14.Immunogenetics 24: 328–330, 1986.

    Google Scholar 

  8. Bessis, A., Simon-Chazottes, D., Devillers-Thiéry, A., Guénet, J.-L., and Changeux, J.-P.: Chromosomal localization of the mouse genes coding for alpha2, alpha3, alpha4, and beta2 subunits of neuronal nicotinic acetylcholine receptor.FEBS Lett 264: 48–52, 1990.

    Google Scholar 

  9. Bishop, D.T.: The information content of phase known matings for ordering genetic loci.Genet Epidemiol 2: 349–361, 1985.

    Google Scholar 

  10. Bode, V.C., Bonhomme, F., and Guénet, J.-L.: Personal communication.Mouse News Lett 74: 97, 1986.

    Google Scholar 

  11. Bode, V.C., McDonald, J.D., Guénet, J.-L., and Simon, D.:hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.Genetics 118: 299–305, 1988.

    Google Scholar 

  12. Boehm, T., Baer, R., Lavenir, I., Forster, A., Waters, J.J., Nacheva, E., and Rabbitts, T.H.: The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C-delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15.EMBO J 7: 385–394, 1988.

    Google Scholar 

  13. Bowcock, A.M., Farrer, L.A., Hebert, J.M., Agger, M., Sternlieb, I., Scheinberg, I.H., Buy, C.H.C.M., Scheffer, H., Frydman, M., Chajek-Saul, T., Bonne-Tamir, B., and Cavalli-Sforza, L.L.: Eight closely linked loci place the Wilson disease locus within 13q14-q21.Am J Hum Genet 43: 664–674, 1988.

    Google Scholar 

  14. Brand, N., Petkovich, M., Krust, A., Chambon, P., de Thé, H., Marchio, A., Tiollais, P., and Dejean, A.: Identification of a second human retinoic acid receptor.Nature 332: 850–853, 1988.

    Google Scholar 

  15. Bremmer, T.A., Premkumar-Reddy, E., Nayar, K., and Kouri, R.E.: Nucleoside phosphorylase 2 (Np-2) in mice.Biochem Genet 16: 1143–1151, 1978.

    Google Scholar 

  16. Brooke, H.C.: Hairless mice.J Hered:17: 173–174, 1926.

    Google Scholar 

  17. Brunet, J.-F., Dosseto, M., Denizot, F., Mattei, M.-G., Clark, W.R., Haqqi, T.M., Ferrier, P., Nabholz, M., Schmitt-Verhulst, A.-M., Luciani, M.-F., and Golstein, P.: The inducible cytotoxic T-lymphocyte-associated gene transcript CTLA-1 sequence and gene localization to mouse chromosome 14.Nature 322: 268–271, 1986.

    Google Scholar 

  18. Bruns, G., Stroh, H., Veldman, G., Latt, S.A., and Floros, J.: The 35k pulmonary surfactant-associated protein is encoded on chromosome 10.Hum Genet 76: 58–62, 1987.

    Google Scholar 

  19. Carson, N.L. and Simpson, N.E.: A physical map of 14 markers on chromosome 10 from dosage studies on abnormal cell lines.Cytogenet Cell Genet 40: 974–975, 1989.

    Google Scholar 

  20. Cattanach, B.M.: Crossover suppression in mice heterozygous for tobacco mouse metacentrics.Cytogenet Cell Genet 20: 264–281, 1978.

    Google Scholar 

  21. Cattanach, B.M., Iddon, C.A., Charlton, H.M., Chiappa, S.A., and Fink, G.: Gonadotropin-releasing hormone deficiency in a mutant mouse with hypogonadism.Nature 269: 338–340, 1986.

    Google Scholar 

  22. Ceci, J.D., Kingsley, D.M., Silan, C.M., Copeland, N.G., and Jenkins, N.A.: An interspecific backcross linkage map of the proximal half of mouse chromosome 14.Genomics 6: 673–678, 1990.

    Google Scholar 

  23. Chan, T.-S., Creagan, R.P., and Reardon, M.P.: Adenosine kinase as a new selective marker in somatic cell genetics: isolation of adenosine kinase-deficient mouse cell lines and human-mouse hybrid cell lines containing adenosine kinase.Somatic Cell Genet 4: 1–12, 1978.

    Google Scholar 

  24. Chang, H.-Y., Guerrero, I., Lake, R., Pellicer, A., and D'Eustachio, P.: Mouse N-ras genes: organization of the functional locus and of a truncated cDNA-like pseudogene.Oncogene Res 1: 129–136, 1987.

    Google Scholar 

  25. Chen, S., Creagen, R.P., Nichols, E.A., and Ruddle, F.H.: Assignment of human esterase-D gene to chromosome 13.Cytogenet Cell Genet 14: 269–272, 1975.

    Google Scholar 

  26. Chien, Y.-H., Iwashima, M., Kaplan, K.B., Elliott, J.F., and Davis, M.M.: A new T-cell receptor gene located within the alpha locus and expressed early in T-cell differentiation.Nature 327: 677–682, 1987.

    Google Scholar 

  27. Chin, H., Kozak, C.A., Kim, H.-L., Mock, B., and McBride, O.W.: A brain L-type calcium channel alpha 1 subunit gene (CCHL1A2) maps to mouse Chromosome 14 and human Chromosome 3.Genomics 11: 914–919, 1991.

    Google Scholar 

  28. Collins, M.K.L., Goodfellow, P.N., Spurr, N.K., Solomon, E., Tanigawa, G., Tonegawa, S., and Owen, M.J.: The human T-cell receptor alpha-chain maps to chromosome 14.Nature 314: 273–274, 1985.

    Google Scholar 

  29. Committee on Standardized Genetic Nomenclature for Mice: Standard karyotype of the mouse,Mus musculus.J. Hered 63: 69–72, 1972.

    Google Scholar 

  30. Cox, D.W., Billingsley, G.D., Willard, H.F., and Grzeschik, K.-H.: Localization of markers on chromosome 14.Cytogenet Cell Genet 40: 980, 1989).

    Google Scholar 

  31. Croce, C.M., Isobe, M., Palumbo, A., Puck, J., Ming, J., Tweardy, D., Erikson, J., and Davis, M.: Gene for alpha-chain for T-cell receptor: location on chromosome 14 region involved in T-cell neoplasms.Science 227: 1044–1047, 1985.

    Google Scholar 

  32. Crosby, J.L., Bleackley, R.C., and Nadeau, J.H.: A complex of serine protease genes expressed preferentially in cytotoxic T-lymphocytes is closely linked to the T-cell receptor alpha-and beta-chain genes on mouse chromosome 14.Genomics 6: 252–259, 1990.

    Google Scholar 

  33. Cumming, R.B., Gaertner, F.H., Walton, M.F., and O'Donnell, S.C.: A structural gene for formamidase.Mouse News Lett 56: 53, 1977.

    Google Scholar 

  34. Cumming, R.B., Walton, W.F., Fuscoe, J.C., Taylor, B.A., Womack, J.E., and Gaertner, F.H.: Genetics of formamidase-5 (brain formamidase) in the mouse: localization of the structural gene on chromosome 14.Biochem Genet 17: 415–431, 1979.

    Google Scholar 

  35. Czosnek, H.H., Bienz, B., Givol, D., Zakut-Houri, R., Pravtcheva, D., Ruddle, F.H., and Oren, M.: The gene and the pseudogene for mouse p53 cellular tumor antigen are located on different chromosomes.Mol Cell Biol 4: 1638–1640, 1984.

    Google Scholar 

  36. Danciger, M., Kozak, C.A., Nickerson, J., Redmond, T.M., and Farber, D.B.: Localization of the gene for interphotoreceptor retinoid-binding protein to mouse chromosome 14 nearNp-1.Genomics 8: 727–731, 1990.

    Google Scholar 

  37. Datta, S.K., Owen, F.L., Womack, J.E., and Riblet, R.J.: Analysis of recombinant inbred lines derived from “autoimmune” (NZB) and “high leukemia”. (C58) strain: independent multigenic systems control B cell hyperactivity, retrovirus expression, and autoimmunity.J Immunol 129: 1544, 1982.

    Google Scholar 

  38. Dembic, Z., Bannwarth, W., Taylor, B.A., and Steinmetz, M.: The gene encoding the T-cell receptor alpha-chain maps close to theNp-2 locus on mouse chromosome 14.Nature 314: 271–273, 1985.

    Google Scholar 

  39. de Thé, H., Marchio, A., Tiollais, P., and Dejean, A.: A novel steroid thyroid hormone receptor-related gene inappropriately expressed in human heptocellular carcinoma.Nature 330: 667–670, 1987.

    Google Scholar 

  40. Dickie, M.M.: Gunmetal.Mouse News Lett 30: 30, 1964.

    Google Scholar 

  41. Dickie, M.M., Schneider, J., and Harman, P.J.: A juvenile wabbler-lethal in the house mouse.J Hered 43: 283–286, 1952.

    Google Scholar 

  42. Dickinson, M.E., Kobrin, M.S., Silan, C.M., Kingsley, D.M., Justice, M.J., Miller, D.A., Ceci, J.D., Lock, L.F., Lee, A., Buchberg, A.M., Siracusa, L.D., Lyons, K.M., Derynck, R., and Hogan, B.L.M.: Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci.Genomics.6: 505–520, 1990.

    Google Scholar 

  43. Dietrich, W., Katz, H., Lincoln, S.E., Shin, H.-S., Friedman, J., Dracopoli, N., and Lander, E.S.: A genetic map of the mouse suitable for typing intraspecific crosses.Genetics, in press, 1992.

  44. Dunn, L.C.: Types of white spotting in mice.Am Naturalist 54: 465–495, 1920.

    Google Scholar 

  45. Dymecki, S.M., Niederhuber, J.E., and Desiderio, S.V.: Specific expression of a tyrosine kinase gene,blk, in B lymphoid cells.Science 247: 332–336, 1990.

    Google Scholar 

  46. Eicher, E.M.: Personal communication, 1972.

  47. Eicher, E.M., and Green, M.C.: TheT6 translocation in the mouse: its use in trisomy mapping, centromere localization, and cytological identification of linkage group III.Genetics 71: 621–632, 1972.

    Google Scholar 

  48. Elliott, R.: Identification and mapping of new loci using cloned cDNA.Mouse News Lett 64: 87, 1981.

    Google Scholar 

  49. Elliott, R.W., Samuelson, L.C., Lambert, M.S., and Meisler, M.H.: Assignment of pancreatic ribonuclease gene to mouse chromosome 14.Cytogenet Cell Genet 42: 110–112, 1986.

    Google Scholar 

  50. Eppig, J.T. and Eicher, E.M.: Application of the ovarian teratoma mapping method in the mouse.Genetics 103: 797–812, 1983.

    Google Scholar 

  51. Epstein, R., Sham, G., Womack, J., Yaguë, J., Palmer, E., and Cohn, M.: The cytotoxic T cell response to the male-specific histocompatibility antigen (H-Y) is controlled by two dominant immune response genes, one in the MHC, the other in the T-alpha locus.J Exp Med 163: 759–773, 1986.

    Google Scholar 

  52. Farrer, L.A., Castiglione, C.M., Kidd, J.R., Myers, S., Carson, N., Simpson, N.E., and Kidd, K.K.: A linkage group of five DNA markers on human chromosome 10.Genomics 3: 72–77, 1988.

    Google Scholar 

  53. Fisher, J.H., Kao, F.T., Jones, C., White, R.T., Benson, B.J., and Mason, R.J.: The coding sequence for the 32,000 Dalton pulmonary surfactant-associated protein A is located on chromosome 10 and identifies two separate restriction fragment length polymorphisms.Am J Hum Genet 40: 503–511, 1987.

    Google Scholar 

  54. Fisher, J.H., Emrie, P.A., Drabkin, HA., Kishnik, T., Gerber, M., Hofmann, T., and Jones, C.: The gene encoding the hydrophobic surfactant protein SP-C is located on 8p and identifies andEcoRI RFLP.Am J Hum Genet 43: 436–441, 1988.

    Google Scholar 

  55. Francke, U., Busby, N., Shaw, D., Hansen, S., and Brown, M.G.: Intrachromosomal gene mapping in man: assignment of nucleoside phosphorylase to region 14cen→14q21 by interspecific hybridization of cells with a t(X;14)(p22;q21) translocation.Somatic Cell Genet 2: 27–40, 1976.

    Google Scholar 

  56. Francke, U., Lalley, P.A., Moss, W., Ivy, J., and Minna, J.D.: Gene mapping inMus musculus by interspecific cell hybridization: assignment of the gene tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2.Cytogenet Cell Genet 19: 57–84, 1977.

    Google Scholar 

  57. Francke, U. and Thompson, L.: Regional mapping by exclusion of adenosine kinase (ADOK) on human chromosome 10 using gene dosage.Cytogenet Cell Genet 25: 156, 1979.

    Google Scholar 

  58. Frankel, W.N., Coffin, J.M., Cote, M., Seyfried, T.N., Rise, M., Rajan, T.V., Nelson, F.K., Selsing, E., and Gerstein, R.: Bockcross data for endogenousMpmv, Pmv andXmv proviruses.Mouse Genome 89: 266–270, 1991.

    Google Scholar 

  59. Frankel, W.N., Stoye, J.P., Taylor, B.A., and Coffin, J.M.: Genetic analysis of endogenous xenotropic murine leukemia viruses: association with two common mouse mutations and the viral restriction locusFv-1.J Virol 63: 1763–1774, 1989a.

    Google Scholar 

  60. Frankel, W.N., Stoye, J.P., Taylor, B.A., and Coffin, J.M.: Genetic identification of endogenous polytropic proviruses by using recombinant inbred mice.J Virol 63: 3810–3821, 1989b.

    Google Scholar 

  61. Frecker, M., Dallaire, L., Young, S.R., Chen, G.C.C., and Simpson, N.E.: Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies.Hum Genet 45: 167–173, 1978.

    Google Scholar 

  62. Friend, S.H., Bernards, R., Rogelj, S., Weinberg, R.A., Rapaport, J.M., Albert, D.M., and Dryja, T.P.: A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma.Nature 323: 643–646, 1986.

    Google Scholar 

  63. Gey, W.: Multipelle Missbildungen und Retinoblastom.Humangenetik 10: 362–365, 1970.

    Google Scholar 

  64. Glasser, S.W., Korfhagen, T.R., Bruno, M.D., Dey, C., and Whitsett, J.A.: Structure and expression of the pulmonary surfactant protein SP-C gene in the mouse.J Biol Chem 265: 21986–21991, 1990.

    Google Scholar 

  65. Gleditsch, L., Snodgrass, R., and Bogen, B.: No recombinations betweenTcra-V andTcra-C gene segments in 699 backcross mice.Immunogenetics 32: 297–303, 1990.

    Google Scholar 

  66. Green, M.C.: Personal communication.Mouse News Lett 34: 31, 1966.

    Google Scholar 

  67. Green, M.C.: Personal communication.Mouse News Lett 44: 30, 1971.

    Google Scholar 

  68. Green, M.C.: Slaty (slt).Mouse News Lett 47: 36, 1972a.

    Google Scholar 

  69. Green, M.C.: Waved coat (Wc).Mouse News Lett 48: 36, 1972b.

    Google Scholar 

  70. Green, M.C.: Chromosome 14.Mouse News Lett 48: 35, 1973a.

    Google Scholar 

  71. Green, M.C.: Personal communication.Mouse News Lett, 49: 32, 1973b.

    Google Scholar 

  72. Green, M.C.: Personal communication.Mouse News Lett 51: 23, 1974.

    Google Scholar 

  73. Green, M.C. and Sweet, H.O.: Chromosome 14.Mouse News Lett 55: 17, 1976.

    Google Scholar 

  74. Hanauer, A., Mandel, J.-L., and Mattei, M.-G.: X linked and autosomal sequences corresponding to glutamate dehydrogenase (GLUD) and to an anonymous cDNA.Cytogenet Cell Genet 40: 647–648, 1985.

    Google Scholar 

  75. Hanauer, A., Mattei, M.-G., and Mandel, J.-L.: Presence of aTaqI polymorphism in the human glutamate dehydrogenase (FLUD) gene on chromosome 10.Nucleic Acids Res 15: 6308, 1987.

    Google Scholar 

  76. Harper, K., Mattei, M.-G., Simon, D., Suzan, M., Guénet, J.-L., Haddad, P., Sasportes, M., and Golstein, P.: Proximity of the CTLA-1 serine protease andTcr alpha loci in mouse and man.Immunogenetics 28: 439–444, 1988.

    Google Scholar 

  77. Hayday, A.C., Diamond, D.J., Tanigawa, G., Heilig, J.S., Folsom, V., Saito, H., and Tonegawa, S.: Unusual organization and diversity of T-cell receptor alpha-chain genes.Nature 316: 828–832, 1985.

    Google Scholar 

  78. Hearne, C.M., McAleer, M.A., Love, J.M., Aitman, T.J., Cornall, R.J., Ghosh, S., Knight, A.M., Prins, J.-B., and Todd, J.A.: Additional microsatellite markers for mouse genome mapping.Mammalian Genome 1: 273–282, 1991.

    Google Scholar 

  79. Heidmann, O., Buonanno, A., Geoffroy, B., Robert, B., Guénet, J.-L., Merlie, J.P., and Changeux, J.-P.: Chromosomal localization of muscle nicotinic acetylcholine receptor genes in the mouse.Science 234: 866–868, 1986.

    Google Scholar 

  80. Hoecker, G., Martinez, A., Markovic, S., and Pizarro, O.: Agitans, a new mutation in the house mouse with neurological effects.J Hered 45: 10–14, 1954.

    Google Scholar 

  81. Hsieh, C.-L., Bowcock, A.M., Farrer, L.A., Hebert, J.M., Huang, K.N., Cavalli-Sforza, L.L., Julius, D., and Francke, U.: The serotonin receptor subtype 2 locusHTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14.Somatic Cell Mol Genet 16: 567–574, 1991a.

    Google Scholar 

  82. Hsieh, C.-L., Kumar, N.M., Gilula, N.B., and Francke, U.: Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes.Somatic Cell Mol Genet 17: 191–200, 1991b.

    Google Scholar 

  83. Hsieh, C.-L., Lee, W.H., Lee, E.Y.-H.P., Killary, A.M., Lalley, P.A., and Naylor, S.A.: Assignment of retinoblastoma susceptibility gene to mouse chromosome 14.Somatic Cell Mol Genet 15: 461–464, 1989.

    Google Scholar 

  84. Hummel, K.P.: The inheritance and expression of disorganization, an unusual mutation in the mouse.J Exp Zool 137: 389–423, 1958.

    Google Scholar 

  85. Hummel, K.P.: Personal communication, 1965.

  86. Hurst, J., Flavell, D., Julien, J.P., Meijer, P., Mushinski, W., and Grosveld, F.: The human neurofilament gene (NFL) is located on the short arm of chromosome 8.Cytogenet Cell Genet 45: 30–32, 1987.

    Google Scholar 

  87. Jackson, I.J., Chambers, D.M., Tsukamoto, K., Copeland, N.G., gilbert, D.J., Jenkins, N.A., and Hearing, V.: A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus.EMBO J 11: 527–535, 1992.

    Google Scholar 

  88. Jeffreys, A.J., Wilson, V., Kelly, R., Taylor, B.A., and Bulfield, G.: Mouse DNA “fingerprints”: analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains.Nucleic Acids Res 15: 2823–2836, 1987.

    Google Scholar 

  89. Jenne, D.E., Zimmer, M., Garcia-Sanz, J.A., Tschopp, J., and Lichter, P.: Genomic organization and subchromosomal in situ localization of the murine granzyme F., a serine protease expressed in CD8+ T cells.J Immunol 147: 1045–1052, 1991.

    Google Scholar 

  90. Jouvin-Marche, E., Hue, I., Marche, P.N., Liebe-Gris, C., Marolleau, J.-P., Malissen, B., Cazenave, P.-A., and Malissen, M.: Genomic organization of the mouse T cell receptor V alpha family.EMBO J 9:2141–2150, 1990.

    Google Scholar 

  91. Kidwell, J.F., Gowen, J.W., and Stadler, J.: Pugnose—a recessive mutation in linkage group 3 of mice.J Hered 52: 145–148, 1961.

    Google Scholar 

  92. Kidwell, J.F., Gowen, J.W., and Stadler, J.: Pugnose linkage in the mouse.J Hered 57: 229–230, 1967.

    Google Scholar 

  93. Kozak, C., Danciger, M., and Farber, D.: Chromosome assignment in the mouse of the genes for several proteins involved in visual transduction.Cytogenet Cell Genet 10: 1025–1026, 1989.

    Google Scholar 

  94. Kozak, C.A., Dymecki, S.M., Niederhuber, J.E., and Desiderio, S.V.: Genetic mapping of the gene for a novel tyrosine kinase,Blk, to mouse chromosome 14.Genomics 9: 762–764, 1991.

    Google Scholar 

  95. Kozak, C.A. and Ruddle, F.H.: Sexual and parasexual approaches to the genetic analysis of the laboratory mouse,Mus musculus.In Vitro 12: 720–725, 1976.

    Google Scholar 

  96. Krangel, M.S., Band, H., Hata, S., McLean, J., and Brenner, M.B.: Structurally divergent human T-cell receptor gamma proteins encoded by distinct C-gamma genes.Science 237: 64–67, 1987.

    Google Scholar 

  97. Kranz, D.M., Saito, H., Disteche, C.M., Swisshelm, K., Pravtcheva, D., Ruddle, F.H., Eisen, H.N., and Tonegawa, S.: Chrososomal locations of the murine T-cell receptor alphachain gene and the T-cell gamma gene.Science 227: 941–945, 1985.

    Google Scholar 

  98. Lai, E., Wilson, R.K., and Hood, L.E.: Physical maps of the mouse and human immunoglobulin-like loci.Adv Immunol 46: 1–59, 1989.

    Google Scholar 

  99. Lane, P.W.: Personal communication, 1963.

  100. Lane, P.W.: Personal communication, 1966.

  101. Lane, P.W.: Personal communication, 1970.

  102. Lane, P.W. and Dickie, M.M.: Linkage of wabbler-lethal and hairless in the mouse.J Hered 52: 159–160, 1961.

    Google Scholar 

  103. Lang J.: Assay for deletion inGnrh (hpg) locus using PCR.Mouse Genome 89: 857, 1991.

    Google Scholar 

  104. Lee, W.H., Bookstein, R., Hong, F., Young, L.-J., Shew, J.-Y., and Lee, E.Y.-H.P.: Human retinoblastoma susceptibility gene: cloning, identification and sequencing.Science 235: 1394–1399, 1987.

    Google Scholar 

  105. Lee, B.K. and Eicher, E.M.: Segregation patterns of endogenous mouse mammary tumor viruses in five recombinant inbred strain sets.J Virol 64: 4568–4572, 1990.

    Google Scholar 

  106. Lee, E.Y.-H.P. and Lee, W.H.: Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma.Proc Natl Acad Sci USA 83: 6337–6341, 1986.

    Google Scholar 

  107. Leinwand, L., Fournier, R.E.K., Nichols, E.A., and Ruddle, F.H.: Assignment of the gene for adenosine kinase to chromosome 14 inMus musculus by somatic cell hybridization.Cytogenet Cell Genet 21: 77–85, 1978.

    Google Scholar 

  108. Lewis, W.H., Michalopoulos, E.E., Williams, D.L., Minden, M.D., and Mak, T.W.: Breakpoints in the human T-cell antigen receptor alpha-chain locus in two T-cell leukemia patients with chromosomal translocations.Nature 317: 544–546, 1985.

    Google Scholar 

  109. Liesi, P., Julien, J.-P., Vilja, P., Grosveld, F., and Rechardt, L.: Specific detection of neuronal cell bodies: in situ hybridization with a biotin-labeled neurofilament cDNA probe.J Histochem Cytochem 7: 923–926, 1986.

    Google Scholar 

  110. Liou, G.I., Li, Y., Wang, C., Fong, S.-L., Bhattacharya, S., and Bridges, C.D.B.:BglII RFLP recognized by a human IRBP cDNA localized to chromosome 10.Nucleic Acids Res 15: 3196, 1987.

    Google Scholar 

  111. Liu, J., Chen, Y., Kozak, C.A., and Yu, L.: The 5-HT2 serotonin geneHtr-2 is tightly linked toEs-10 on mouse Chromosome 14.Genomics 11: 231–234, 1991.

    Google Scholar 

  112. Lobe, C.G., Finlay, B.B., Paranchych, W., Paetkau, V.H., and Bleackley, R.C.: Cloning of two genes that are specifically expressed in activated cytotoxic T lymphocytes.Proc Natl Acad Sci USA 83: 1448–1452, 1986.

    Google Scholar 

  113. Love, J.M., Knight, A.M., McLeer, M.A., and Todd, J.A.: Toward construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites.Nucleic Acids Res 18: 4123–4130, 1990.

    Google Scholar 

  114. Lukey, T., Neote, K., Loman, J.F., Unger, A.E., Biddle, F.G., and Snyder, F.F.: Purine nucleoside phosphorylase (Np) in the mouse: linkage relationship ofNp-2 to esterase-10 (Es-10) andNp-1 on chromosome 14.Biochem Genet 23: 347–356, 1985.

    Google Scholar 

  115. Lyon, M.F., and Glenister, P.H.: Roan and freckled.Mouse News Lett 59: 18, 1978.

    Google Scholar 

  116. Lyon, M.F. and Newport, P.R.: Personal communication.Mouse News Lett 49: 30, 1973.

    Google Scholar 

  117. MacGregor, G.R., Russell, L.D., Van Beek, M.E.A.B., Hanten, G.R., Kovac, M.J., Kozak, C.A., Meistrich, M.L., and Overbeek, P.A.: Symplastic spermatids (sys): a recessive insertional mutation in mice causing a defect in spermatogenesis.Proc Natl Acad Sci USA 87: 5016–5020, 1990.

    Google Scholar 

  118. Mason, A.J., Hayflick, J.S., Zoeller, R.T., Young, W.S., Phillips, H., Nikolics, K., and Seeburg, P.H.: A deletion truncating the gonadotropin-releasing hormone gene is responsible for hypogonadism in the hpg mouse.Science 234: 1366–1371, 1986a.

    Google Scholar 

  119. Mason, A.J., Pitts, S.L., Nikolics, K., Szonyi, E., Wilcox, J.N., Seeburg, P.H., and Stewart, T.A.: The hypogonadal mouse: reproductive functions restored by gene therapy.Science 234: 1372–1378, 1986b.

    Google Scholar 

  120. Mathew, C., Nakamura, Y., Easton, D., Wakeling, W., Jones, E., Chin, K., Telenius, H., Clark, J., Smith, B., Strong, C., Bragg, T., Little, P., Jones, C.A., Povey, S., White, R., and Ponder, B.: MEN2A and the developing map of chromosome 10.Cytogenet Cell Genet 40: 1040, 1989.

    Google Scholar 

  121. Matsuoka, R., Chambers, A., Kimura, M., Kanda, N., Bruns, G., Yoshida, M., and Takao, A.: Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy chain.Am J Med Genet 29: 369–376, 1988.

    Google Scholar 

  122. Matsuoka, R., Yoshida, M.C., Kanda, N., Kimura, M., Ozasa, H., and Takao, A.: Human cardiac myosin heavy chain gene mapped within chromosomal region 14q11.2–q13.Cytogenet Cell Genet 40: 1040–1041, 1989a.

    Google Scholar 

  123. Matsuoka, R., Yoshida, M.C., Kanda, N., Kimura, M., Ozasa, H., and Takao, A.: Human cardiac myosin heavy chain gene mapped within chromosomal region 14q11.2–q13.Am J Med Genet 32: 279–284, 1989b.

    Google Scholar 

  124. Mattei, M.-G., de Thé, H., Mattei, J.-F., Marchio, A., Tiollais, P., and Dejean, A.: Assignment of the human hap retinoic acid receptor RAR-beta gene to the p24 band of chromosome 3.Hum Genet 80: 189–190, 1988.

    Google Scholar 

  125. Mattei, M.-G., Duprey, P., Li, Z.L., Mattei, J.-F., and Paulin, D.: Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunit.Biol Cell 67: 235–237, 1989.

    Google Scholar 

  126. Mattei, M.-G., Harper, K., Brunet, J.F., Denizot, F., Mattei, J.-F., Golstein, P., and Giraud, F.: In situ mapping of four cytotoxic T-lymphocyte associated proteins (CTLA) to the mouse genome.Cytogenet Cell Genet 46: 657–658, 1987.

    Google Scholar 

  127. Mattei, M.G., Rivière, M., Krust, A., Ingvarsson, S., Vennström, B., Islam, M.Q., Levan, G., Kautner, P., Zelent, A., Chambon, P., Szpirer, J., and Szpirer, C.: Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomes.Genomics 10: 1061–1069, 1991.

    Google Scholar 

  128. Miret-Duvaux, O., Frederic, F., Simon, D., Guénet, J.-L., Hanauer, A., Delhaye-Bouchaud, N., and Mariani, J.: Glutamate dehydrogenase in cerebellar mutant mice: gene localization and enzyme activity in different tissues.J Neurochem 54: 23–29, 1990.

    Google Scholar 

  129. Moore, K.J., D'Amore-Bruno, M.A., Korfhagen, T.R., Glasser, S.W., Whitsett, J.A., Jenkins, N.A., and Copeland, N.G.: Chromosomal localization of three pulmonary surfactant protein genes in the mouse.Genomics 12: 388–393, 1992.

    Google Scholar 

  130. Nadeau, J.H., Bedigian, H.G., Bouchard, G., Denial, T., Kosowsky, M., Norberg, R., Pugh, S., Sargeant, E., and Paigen, B.: Multilocus markers for mouse genome analysis: PCR amplification based on single primers of arbitary nucleotide sequence.Mammalian Genome 3: 55–64, 1992a.

    Google Scholar 

  131. Nadeau, J.H., Ceci, J.D., and Cox, R.: Mouse Chromosome 14.Mammalian Genome 1 (Suppl): S221-S240, 1991a.

    Google Scholar 

  132. Nadeau, J.H., Compton, J.G., Giguère,V., Rossant, J., and Varmuza, S.: Close linkage of retinoic acid receptor genes with homeobox- and keration-encoding genes on paralogous segments of mouse Chromosomes 11 and 15.Mammalian Genome 3: 202–208, 1992b.

    Google Scholar 

  133. Nadeau, J.H., Herrmann, B., Bucan, M., Burkhart, D., Crosby, J.L., Erhart, M.A., Kosowsky, M., Kraus, J.P., Michiels, F., Schnattinger, A., Tchetgen, M.-B., Varnum, D., Willison, K., Lehrach, H., and Barlow, D.: Genetic maps of mouse Chromosome 17 including 12 new anonymous DNA loci and 25 anchor loci.Genomics 9: 78–89, 1991b.

    Google Scholar 

  134. Nakajima, P.B., Di Vincenzo, J.P., Jameson, S.C., and Gascoigne, N.R.J.: Chromosome 14 in B10.A(18R) mice is recombinant and includesTcra-V a alleles.Immunogenetics 35: 190–198, 1992.

    Google Scholar 

  135. Nakamura, Y., Lathrop, M., Bragg, T., Leppert, M., O'Connell, P., Jones, C., Lalouel, J.-M., and White, R.: An extended genetic linkage map of markers for human chromosome 10.Genomics 3: 389–392, 1988.

    Google Scholar 

  136. Naylor, S.L., Marshall, A., Killary, A.M., Lalley, P.A., Belin, D., Rickles, R., Strickland, S., and Rajput, B.: The genes for mouse plasminogen activator and urokinase map to chromosomes 8 and 14, respectively.Cytogenet Cell Genet 46: 669, 1987.

    Google Scholar 

  137. Nesbitt, M., Pugh, S.L., and Paigen, B.: Strain distribution pattern of thirteen genetic loci in the AXB and BXA recombinant inbred set.Mouse Genome 88: 113, 1990.

    Google Scholar 

  138. Nichols, E.A. and Ruddle, F.H.: A review of enzyme polymorphism, linkage and electrophoretic conditions for mouse and somatic cell hybrids in starch gels.J Histochem Cytochem 21: 1066–1081, 1973.

    Google Scholar 

  139. Nusse, R., Brown, A., Papkoff, J., Scambler, P., Shackleford, G., McMahon, A., Moon, R., and Varmus, H.: A new nomenclature forint-1 and related genes: theWnt gene family.Cell 64: 231, 1991.

    Google Scholar 

  140. Owerbach, D. and Hjorth, J.P.: Genetic determination of a parotid secretory protein in mouse.Hereditas 89: 146, 1978.

    Google Scholar 

  141. Rajput, B., Degen, S.F., Reich, E., Waller, E.K., Axelrod, J., Eddy, R.L., and Shows, T.B.: Chromosomal locations of human tissue plasminogen activator and urokinase genes.Science 230: 672–674, 1985.

    Google Scholar 

  142. Rajput, B., Marshall, A., Killary, A.M., Lalley, P.A., Naylor, S.L., Belin, D., Rickles, R.J., and Strickland, S.: Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse.Somatic Cell Mol Genet 13: 581–586, 1987.

    Google Scholar 

  143. Rasberry, C. and Cattanach, B.: Location of talipes (Tal).Mouse Genome 87: 89, 1990.

    Google Scholar 

  144. Ricciuti, F. and Ruddle, F.H.: Assignment of nucleoside phosphorylase to D-14 and localization of X-linked loci in man by somatic cell genetics.Nature New Biol. 241: 180–182, 1973.

    Google Scholar 

  145. Richards-Smith, B., and Elliott, R.W.: Mapping of repeated sequences in the mouse genome.Mouse News Lett 71: 46–47, 1984.

    Google Scholar 

  146. Roderick, T.H., Hawes, N.L., Davisson, M.T., and Hillyard, A.L.: Map of inversions.In M.F. Lyon and A.G. Searle (eds);Genetic Variants and Strains of the Laboratory Mouse, pp. 626–631, Oxford University Press, Oxford, 1989.

    Google Scholar 

  147. Russell, W.L. and Russell, L.B.: The genetic and phenotypic characteristics of radiation-induced mjtations in mice.Rad Res Suppl 1: 296–305, 1959.

    Google Scholar 

  148. Rutledge, J.C., Cain, K.T., Cachiero, N.L.A., Cornett, C.V., Wright, C.G., and Generoso, W.M.: A balanced translocation in mice with a neurological defect.Science 231: 395–397, 1985.

    Google Scholar 

  149. Ryan, J., Hart, C.P., and Ruddle, F.H.: Molecular cloning and chromosomal assignment of murineN-ras.Nucleic Acids Res 12: 6063–6072, 1984.

    Google Scholar 

  150. Saez, L.J., Gianola, K.M., McNalley, E.M., Feghali, R., Eddy, R., Shows, T.B., and Leinwand, L.: Human cardiac myosin heavy chain genes and their linkage in the genome.Nucleic Acids Res 15: 5443–5459, 1987.

    Google Scholar 

  151. Salier, J.-P.: Personal communication, 1992.

  152. Samuelson, L.C. and Farber, R.A.: Cytological localization of three genes on chromosome 14 inMus musculus. Am J Hum Genet 36: 207s, 1984.

  153. Samuelson, L.C. and Farber, R.A.: Cytological localization of adenosine kinase, nucleoside phosphorylase-1 and esterase-10 genes on mouse chromosome 14.Somatic Cell Mol Genet 11: 157–165, 1985.

    Google Scholar 

  154. Searle, A.G. and Beechey, C.V.: Maps of chromosomal variants.In M.F. Lyon and A.G. Searle (eds.);Genetic Variants and Strains of the Laboratory Mouse, pp. 620–625, Oxford University Press, Oxford, 1989.

    Google Scholar 

  155. Sebastio, G., Riccio, A., Verde, P., Scarpato, N., and Blasi, F.:BamHI RFLP linked to the human urokinase gene.Nucleic Acids Res 13: 5404, 1985.

    Google Scholar 

  156. Seldin, M.: Personal communication, 1990.

  157. Serikawa, T., Montagutelli, X., Simon-Chazottes, D., and Guénet, J.-L.: Polymorphisms revealed by PCR with single, short sized, arbitrary primers are reliable markers for mouse and rat gene mapping.Mammalian Genome 3: 65–72, 1992.

    Google Scholar 

  158. Shaughnessy, J., Mock, B., Duncan, R., Potter, M., and Banner, C.: A restriction fragment length polymorphism at murineGlud locus co-segregates withRib-1, Es-10, andTcra on chromosome 14.Nucleic Acids Res 17: 2881, 1989.

    Google Scholar 

  159. Silver, J., and Buckler, C.E.: Statistical considerations for linkage analysis using recombinant inbred strains and backcrosses.Proc Natl Acad Sci USA 83: 1423–1427, 1986.

    Google Scholar 

  160. Siracusa, L.D., Buchberg, A.M., Copeland, N.G., and Jenkins, N.A.: Recombinant inbred strain and interspecific backcross cross analysis of molecular markers flanking the murine agouti coat color locus.Genetics 122: 669–679, 1989.

    Google Scholar 

  161. Siracusa, L.D., Jenkins, N.A., and Copeland, N.G.: Identification and application of repetitive probes for gene mapping in the mouse.Genetics 127: 169–179, 1991a

    Google Scholar 

  162. Siracusa, L.D., Rosner, M.H., Vigano, M.A., Gilbert, D.J., Staudt, L.M., Copeland, N.G., and Jenkins, N.A.: Chromosomal location of the octamer transcription factors,Otf-1, Otf-2 andOtf-3 defines multipleOtf-3- related sequences dispersed in the mouse genome.Genomics 10: 313–326, 1991b.

    Google Scholar 

  163. Snell, G.D.: Inheritance in the house mouse, the linkage of short-ear, hairless, and naked.Genetics 16: 42–74, 1931.

    Google Scholar 

  164. Snell, G.D. and Bunker, H.P.: Histocompatibility genes of mice. V. Five new histocompatibility loci identified by congenic resistant lines on a C57BL/10 background.Transplantation 3: 235–252, 1965.

    Google Scholar 

  165. Snyder, F.: Regulation of purine metabolism.Mouse News Lett 65: 10, 1981.

    Google Scholar 

  166. Snyder, F.F., Biddle, F.G., Lukey, T., and Sparling, M.J.: Genetic variability of purine nucleoside phosphorylase activity in the mouse: relationship to NP-1 and NP-2.Biochem Genet 21: 323–332, 1983.

    Google Scholar 

  167. Snyder, F.F., Lin, C.C., Rudd, N.L., Shearer, J.E., Heikkila, E.M., and Hoo, J.J.: A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic phosphatase and adenosine kinase.Hum Genet 67: 187–189, 1984.

    Google Scholar 

  168. Somerville, M.J., McLachlan, D.R., and Percy, M.E.: Localization of the 68,000-Da human neurofilament gene (NF68) using a murine cDNA probe.Genome 30: 499–500, 1988.

    Google Scholar 

  169. Sorokina, J.D. and Blandova, Z.K.: Personal communication.Mouse News Lett 73: 23, 1985.

    Google Scholar 

  170. Sparkes, R.S., Lan, N., Klisak, I., Mohandas, T., Diep, A., Kojis, T., Heinzmann, C., and Shih, J.C.: Assignment of a serotonin 5HT-2 receptor gene (HTR2) to human chromosome 13q14-q21 and mouse chromosome 14.Genomics 9: 461–465, 1991.

    Google Scholar 

  171. Steinhelper, M.A., and Field, L.J.: Assignment of the angiogenin gene to mouse Chromosome 14 using a rapid PCR-RFLP mapping technique.Genomics 12: 177–179, 1992.

    Google Scholar 

  172. Stone, J.C., Crosby, J.L., Kozak, C.A., Schievella, A., Bernards, R., and Nadeau, J.H.: The murine retinoblastoma homolog maps to chromosome 14 nearEs-10.Genomics 5: 70–75, 1989.

    Google Scholar 

  173. Stoye, J.P., Fenner, S., Greenoak, G.E., Moran, C., and Coffin, J.M.: Role of endogenous retroviruses as mutagens: the hairless mutation of mice.Cell 54: 383–391, 1988.

    Google Scholar 

  174. Strobel, M.: Personal communication, 1990.

  175. Tabas, J.A., Zasloff, M., Wasmuth, J.J., Emanuel, B.S., Altherr, M.R., McPherson, J.D., Wozney, J.M., and Kaplan, F.S.: Bone morphogenetic protein: chromosomal localization of human genes for BMP1, BMP2A, and BMP3.Genomics 9: 283–289, 1991.

    Google Scholar 

  176. Taylor, B.A.: Linkage ofNp-2.Mouse News Lett 65: 28, 1981.

    Google Scholar 

  177. Todd, J.A., Aitman, T.J., Cornall, R.J., Ghosh, S., Hall, J.R.S., Hearne, C.M., Knight, A.M., Love, J.M., McAleer, M.A., Prins, J.-B., Rodrigues, N., Lathrop, M., Pressey, A., DeLarato, N.H., Peterson, L.B., and Wicker, L.S.: Genetic analysis of autoimmune type 1 diabetes mellitus in mice.Nature 351: 542–547, 1991.

    Google Scholar 

  178. Traina, V.L., Taylor, B.A., and Cohen, J.C.: Genetic mapping of endogenous mammary tumor viruses: locus characterization, segregation, and chromosomal distribution.J Virol 40: 735–744, 1981.

    Google Scholar 

  179. Traystman, M.D., Chow, L.H., McManus, B.M., Herskowitz, A., Nesbitt, M.N., and Beisel, K.W.: Susceptibility to coxsackievirus 83-induced chronic myocarditis maps near the murineTcra-alpha andMyhc-alpha loci on Chromosome 14.Am J Pathol 138: 721–726, 1991.

    Google Scholar 

  180. Tripputi, P., Blasi, F., Verde, P., Cannizzaro, L.A., Emanuel, B.S., and Crose, C.M.: Human urokinase gene located on the long arm of chromosome 10.Proc Natl Acad Sci USA 82: 4448–4452, 1985.

    Google Scholar 

  181. Tzimagiorgis, G., Adamson, M.C., Kozak, C.A., and Moschonas, N.K.: Chromosomal mapping of glutamate dehydrogense gene sequences to mouse Chromosomes 7 and 14.Genomics 10: 83–88, 1991.

    Google Scholar 

  182. Ward, P., Packman, S., Loughman, W., Sparkes, M., Sparkes, R., McMahon, A., Gregory, T., and Ablin, A.: Location of the retinoblastoma susceptibility genes(s) and the human esterase D locus.J Med Genet 21: 92–95, 1984.

    Google Scholar 

  183. Weller, P.A., Ogryzko, E.P., Corben, E.B., Zhidkova, N.I., Patel, B., Price, G.J., Spurr, N.K., Koteliansky, V.E., and Critchley, D.R.: Complete sequence of human vinculin and assignment of the gene to chromosome 10.Proc Natl Acad Sci USA 87: 5667–5671, 1990.

    Google Scholar 

  184. Welsh, J., and McClelland, M.: Genomic fingerprinting using arbitrarily primed PCR and a matrix of pairwise combinations of primers.Nucleic Acids Res 19: 5275–5279, 1991.

    Google Scholar 

  185. Weremowicz, S., Fox, E.A., Morton, C.C., and Vallee, B.L.: Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/beta locus.Am J Hum Genet 47: 973–981, 1990.

    Google Scholar 

  186. Weydert, A., Daubas, P., Lazaridis, I., Barton, P., Garner, I., Leader, D.P., Bonhomme, F., Catalan, J., Simon, D., Guénet, J.-L., Gros, F., and Buckingham, M.E.: Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.Proc Natl Acad Sci USA 82: 7183–7187, 1985.

    Google Scholar 

  187. Williamson, P., Lang, J., and Boyd, Y.: The gonadotropin-releasing hormone (Gnrh) gene maps to mouse Chromosome 14 and identifies a homologous region on human Chromosome 8.Somatic Cell Mol Genet 17: 609–615, 1991.

    Google Scholar 

  188. Womack, J.E., Davisson, M.T., Eicher, E.M., and Kendall, D.A.: Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14.Biochem Genet 15: 347–355, 1977.

    Google Scholar 

  189. Womack, J.E., and Sharp, M.: Comparative autosomal linkage in mammals: genetics of esterases inMus musculus andRattus norvegicus.Genetics 82: 665–675, 1976.

    Google Scholar 

  190. Woodward, S.R., Sudweeks, J., and Teuscher, C.: Random sequence oligonucleotide primers detect polymorphic DNA products which segregate in inbred strains of mice.Mammalian Genome 3: 73–78, 1992.

    Google Scholar 

  191. Wozney, J.M., Rosen, V., Celeste, A.J., Mitsock, L.M., Whitters, M.J., Kriz, R.W., Hewick, R.M., and Wang, E.A.: Novel regulators of bone formation: molecular clones and activities.Science 242: 1528–1534, 1988.

    Google Scholar 

  192. Yang-Feng, T.L., Seeburg, P.H., and Francke, U.: Human luteinizing hormone-releasing gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2-p21).Somatic Cell Mol Genet 12: 95–100, 1986.

    Google Scholar 

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Nadeau, J.H., Cox, R. Mouse Chromosome 14. Mammalian Genome 3 (Suppl 1), S206–S219 (1992). https://doi.org/10.1007/BF00648432

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