Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

Mouse chromosome 11

This is a preview of subscription content, log in to check access.


  1. Adler, I.D. and Neuhäuser-Klaus: Seventeen stocks of mice with reciprocal or Robertsonian translocations.Mouse News Lett 77: 139–142, 1987.

  2. Adolf, S. and Klein, J.: Robertsonian variation inMus musculus from Central Europe, Spain and Scotland.J Hered 72: 219–221, 1981.

  3. Archer, B.T., III, Ozcelik, T., Jahn, R., Francke, U., and Sudhof, T.C.: Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2.J Biol Chem 265: 17267–17273, 1990.

  4. Artwert, F., Porck, H.J., Frater-Schroder, M., Brahe, C., Geurts van Kessel, A., Westerveld, A., Meera Khan, P., Zang, K., Frants, R.R., Kortbeek, H.T., and Eriksson, A.W.: Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells.Hum Genet 74: 378–381, 1986.

  5. Ashworth, A. and Willison, K.: Chromosomal localization of mouse cDNAs homologous to theDrosophila gene Krüppel.Mouse News Lett 79: 84, 1987.

  6. Ashworth, A. and Willison, K.: Cloning of zinc finger related genes expressed during mouse embryogenesis.Mouse News Lett 82: 82, 1988.

  7. Ashworth, A., Williams, B.P., Buchberg, A.M., Goodfellow, P.N., Solomon, E., Potter, J., and Willison, K.R.: Chromosomal localization of zinc finger protein genes in man and mouse.Genomics 4: 323–327, 1989.

  8. Bailey, D.W. and Bunker, H.P.: Located histocompatibility genes.Mouse News Lett 47: 18, 1972.

  9. Barker, D., Wright, E., Nguyen, K., Cannon, L., Fain, P., Goldgar, D., Bishop, D.T., Carey, J., Baty, B., Kivlin, J., Willard, H., Waye, J.S., Greig, G., Leinwand, L., Nakamura, Y., O'Connell, P., Leppert, M., Lalouel, J.-M., White, R., and Skolnick, M.: Gene for von Recklinghausen neurofibromatosis is the pericentromeric region of chromosome 17.Science 236: 1100–1102, 1987.

  10. Barletta, C., Batticane, N., Ragusa, R.M., Leube, R.E., Peschle, C., and Romano, V.: Subchromosomal localization of two human cytokeratin genes (KRT4 andKRT15) by in situ hybridization.Cytogenet Cell Genet 54: 148–150, 1990.

  11. Barlow, D.P., Bucan, M., Lehrach, H., Hogan, B.L.M., and Gough, N.M.: Close genetic and physical linkage between the murine haemopoietic growth factor genesGM-CSF and MULTI-CSF (IL3).EMBO J 6: 617–623, 1987.

  12. Bartke, A.: Histology of the anterior hypophysis, thyroid and gonads of two types of dwarf mice.Anatomy Rec 149: 225–235, 1964.

  13. Bartke, A.:df andRe.Mouse News Lett 32: 52–53, 1965.

  14. Bartolomei, M.S. and Corden, J.L.: Localization of an α-amanitin resistance mutation in the gene encoding the largest subunit of mouse RNA polymerase II.Mol Cell Biol 7: 586–594, 1987.

  15. Beechey, C.V. and Searle, A.G.:Mouse News Lett 59: 19–20, 1978.

  16. Beechey, C.V. and Searle, A.G.:Mouse News Lett 70: 81, 1984.

  17. Beechey, C.V. and Searle, A.G.:Mouse News Lett 72: 103–104, 1985.

  18. Beeson, D., Jeremiah, S., West, L.F., Povey, S., and Newsom-Davis, J.: Assignment of the human nicotinic acetylcholine receptor genes: The α and δ subunit genes to chromosome 2 and the β subunit gene to chromosome 17.Ann Hum Genet 54: 199–208, 1990.

  19. Bell, G.I., Murray, J.C., Nakamura, Y., Kayano, T., Eddy, R.L., Fan, Y.S., Byers, M.G., and Shows, T.B.: Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13.Diabetes 38: 1072–1075, 1989.

  20. Benchimol, S., Lamb, P., Crawford, L.V., Sheer, D., Shows, T.B., Bruns, G.A.P., and Peacock, J.: Transformation associated p53 protein is encoded by a gene on human chromosome 17.Som Cell Mol Genet 11: 505–509, 1985.

  21. Bernier, L., Colman, D.R., and D'Eustachio, P.: Chromosomal locations of genes encoding 2′,3′ cyclic nucleotide 3′-phosphodiesterase and glial fibrillary acidic protein in the mouse.J Neurosci Res 20: 496–504, 1988.

  22. Berube, D., Seralini, G.E., Gagne, R., and Hammond, G.L.: Localization of the human sex hormone-binding globulin gene (SHBG) to the short arm of chromosome 17 (17p12–p13).Cytogenet Cell Genet 54: 65–67, 1990.

  23. Biddle, F.:Es-3-oe-co linkage.Mouse News Lett 46: 20, 1972.

  24. Blatt, C., Mileham, K., Haas, M., Nesbitt, M.N., Harper, M.E., and Simon, M.I.: Chromosomal mapping of the mink cell focusinducing and xenotropicenv gene family in the mouse.Proc Natl Acad Sci USA 80: 6298–6302, 1983.

  25. Bogarad L.D., Utset, M.F., Awgulewitsch, A., Miki, T., Hart, C.P., and Ruddle F.H.: The developmental expression pattern of a new murine homeo box gene:Hox-2.5.Devel Biol 133: 537–549, 1989.

  26. Boone, C., Chen, T.R., and Ruddle, F.H.: Assignment of three human genes to chromosomes (LHD-A to 11,TK to 17, andIDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids.Proc Natl Acad Sci USA 69: 510–514, 1972.

  27. Brooker, P.C. and Berry, R.J.:Mouse News Lett 64: 65–66, 1981.

  28. Brooker, P.C.: Robertsonian translocation inMus musculus from N.E. Scotland and Orkney.Heredity 48: 305–309, 1982.

  29. Brownell, E., Kozak, C.A., Fowle, J.R., III, Modi, W.S., Rice, N.R., and O'Brien, S.J.: Comparative genetic mapping of cellularrel sequences in man, mouse, and the domestic cat.Am J Hum Genet 39: 194–202, 1986.

  30. Buchberg, A.M., Bedigian, H.G., Taylor, B.A., Brownell, E., Ihle, J.N., Nagata, S., Jenkins, N.A., and Copeland, N.G.: Localization ofEvi-2 to Chromosome 11: Linkage to other protooncogenes and growth factor loci using interspecific backcross mice.Oncogene Res 2: 149–165, 1988.

  31. Buchberg, A.M., Brownell, E., Nagata, S., Jenkins, N.A., and Copeland, N.G.: A comprehensive genetic map of murine Chromosome 11 reveals extensive linkage conservation between mouse and human.Genetics 122: 153–161, 1989.

  32. Buchberg, A.M., Gilbert, D.J., Cho, B., Jenkins, N.A., and Copeland, N.G.: Abstract: The linkage map of the distal half of mouse chromosome 11 reveals extensive synteny with human chromosome 17. Fourth International Workshop for Mouse Genome Mapping, Annapolis MD, 1990.

  33. Buckle, V.J., Higgs, D.R., Wilkie, A.O., and Weatherall, D.J.: Localisation of human α globin to 16p13.3-pter.J Med Genet 25: 847–849, 1988.

  34. Buckwalter, M.S., Katz, R.W., and Camper, S.A.: Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backross.Genomics 10: 515–526, 1991.

  35. Budarf, M., Emanuel, B.S., Mohandas, T., Goeddel, D.V., and Lowe, D.G.: Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint on 22q.Cytogenet Cell Genet 52: 19–22, 1989.

  36. Cannizzaro, L.A., Emanuel, B.S., Cho, K.W.Y., and Weinmann, R.: The gene encoding the large subunit of human RNA polymerase II is located on the short arm of chromosome 17.Am J Hum Genet 38: 812–818, 1986.

  37. Capanna, E., Cristaldi, M., Perticone, P., and Rizone, M., Identification of chromosomes involved in the 9 Robertsonian fusions of the Apennine mouse with a 22-chromosome karyotype.Experientia 31: 294–296, 1975.

  38. Capanna, E., Gropp, A., Winking, H., Noack, G., and Civitelli, M.V.: Robertsonian metacentrics in the mouse.Chromosoma 58: 341–353, 1976.

  39. Carlin, C.R., Aden, D.P., and Knowles, B.B.: Abstract: S6 is the human receptor for epidermal growth factor (EGF).Cytogenet Cell Genet 32: 256, 1982.

  40. Carter, T.C.: Wavy-coated mice: Phenotypic interactions and linkage tests between rex and (a) waved-1, (b) waved-2.J Genet 50: 268–276, 1951.

  41. Carter, T.C. and Phillips, R.J.S.: The sex distribution of waved-2, shaker-2 and rex in the house mouse.Z. Indukt Abstammungs-Vererbungsl 85: 564–578, 1953.

  42. Cattanach, B.M.: Chemically induced mutations in mice.Mutat Res 3: 346–353, 1966.

  43. Cattanach, B.M. and Moseley, H.J.: Assignment of LG VII to Chromosome 11.Mouse News Lett 48: 31, 1973.

  44. Cattanach, B.M. and Kirk, M.: Differential activity of maternally and paternally derived chromosome regions in mice.Nature 315: 496–498, 1985.

  45. Chang, K.S., Schroeder, W., Siciliano, M.J., Thompson, L.H., McCredie, K., Beran, M., Freireich, E.J., Liang, J.C., Trujillo, J.M., and Stass, S.A.: The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia.Leukemia 1: 458–462, 1987.

  46. Cheng, S.V., Lugo, T.G., Tanzi, R.E., Whitney, J.B., III, Fornier, R.E.K., and Gusella, J.F.: Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker.DNA 6: 401–407, 1987.

  47. Cho, M., Villani, V., and D'Eustachio, P.: A linkage map of distal mouse Chromosome 12.Mammalian Genome 1: 30–36, 1991.

  48. Chrivia, J.C., Uhler, M.D., and McKnight, G.S.: Characterization of genomic clones coding for the Cα and Cβ subunits of mouse cAMP-dependent protein kinase.J Biol Chem 263: 5739–5744, 1988.

  49. Cohen-Haguenauer, O., Barton, P.J.R., Van Cong, N., Cohen, A., Masset, M., Buckingham, M., and Frezal, J.: Chromosomal assignment of two myosin alkali light-chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/fetal muscle isoform (MYL3, MYL4).Hum Genet 81: 278–282, 1989.

  50. Compton, J.G., Phillips, S., and Nadeau, J.H.: Keratin genes. Proximity to mutant loci on Chr 11 and Chr 15 that affect the epidermis, and linkage to homeobox, homolog genes.Mouse News Lett 80: 165–166, 1988.

  51. Coussens, L., Yang-Feng, T.L., Liao, Y.-C., Chen, E., Gray, A., McGrath, J., Seeburg, P.H., Libermann, T.A., Schlessinger, J., Francke, U., Levinson, A., and Ullrich, A.: Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location withneu oncogene.Science 230: 1132–1139, 1985.

  52. Coussens, L., Parker, P.J., Rhee, L., Yang-Feng, T.L., Chen, E., Waterfield, M.D., Francke, U., and Ulrich, A.: Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways.Science 233: 859–866, 1986.

  53. Czosnek, H., Nudel, U., Shani, M., Barker, P.E., Pravtcheva, D.D., Ruddle, F.H., and Yaffe, D.: The genes coding for the muscle contractile proteins, myosin heavy chain myosin light chain 2, and skeletal muscle actin are located on three different mouse chromosomes.EMBO J 1: 1299–1305, 1982.

  54. Czosnek, H.H., Bienz, B., Givol, D., Zakut-Houri, R., Pravtcheva, D.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.

  55. Danciger, M., Tuteja, N., Kozak, C.A., and Farber, D.B.: The gene for the γ-subunit of retinal cGMP-phosphodiesterase is on mouse Chromosome 11.Exp Eye Res 48: 303–308, 1989.

  56. Davies, A.A., Moss, S.E., Crompton, M.R., Jones, T.A., Spurr, N.K., Sheer, D., Kozak, C., and Crumpton, M.J.: The gene coding for the p68 calcium-binding protein is localised to bands q32–q34 of human chromosome 5, and to mouse chromosome 11.Hum Genet 82: 234–238, 1989.

  57. Davisson, M.T., Hawes, N., and Roderick, T.H.:Mouse News Lett 57: 19–20, 1977.

  58. Davisson, M.T. and Akeson, E.C.:Mouse News Lett 69: 26, 1983.

  59. Davison, M.T.: Symbol change forEnv andXp loci.Mouse News Lett 75: 5, 1986.

  60. Davisson, M.T.: New chromosome aberrations.Mouse News Lett 80: 166, 1988.

  61. Davisson, M.T. and Roderick, T.H.: Localization of cytologic breakpoints in induced chromosome rearrangements in the mouse. (Mus musculus). Manuscript in preparation, 1988.

  62. Dayton, A.I., Selden, J.R., Laws, G., Dorney, D.J., Finan, J., Tripputi, P., Emanuel, B.S., Rovera, G., Nowel, P.C., and Croce, C.M.: A human c-erbA oncogene homologue is closely proximal to the chromosome 17 breakpoint in acute promyelocytic leukemia.Proc Natl Acad Sci USA 81: 4495–4499, 1984.

  63. Debuire, B., Henry, C., Benaissa G., Claverie, J.M., Saule, S., Martin, P., and Stehelin, D.: Sequencing theerbA gene of avian erythroblastosis virus reveals a new type of oncogene.Science 224: 1456–1459, 1984.

  64. Deisseroth, A., Nienhuis, A., Turner, P., Velez, R., Anderson, W.F., Ruddle, F.H., Lawrence, J., Creagan, R.P., and Kucherlapati, R.S.: Localization of the human α globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay.Cell 12: 205–218, 1977.

  65. de Jonge, A.J.R., de Smit, S., Kroos, M.A., and Reuser, A.J.J.: Contransfer of syntenic human genes into mouse cell using isolated metaphase chromosomes or cellular DNA.Hum Genet 69: 32–38, 1985.

  66. D'Eustachio, P., Brown, M., Watson, M., and Paul, W.E.: TheIl-4 gene maps to Chromosome 11, near the gene encodingIl-3.J Immunol 141: 3067–3071, 1988.

  67. Dickie, M.M.: Alopecia, a dominant mutation in the house mouse.J Hered 46: 31–34, 1955.

  68. Dickie, M.M. and Deol, M.S.:Mouse News Lett 36: 39, 1967.

  69. Dickie, M.M.: Lustrous, (lt).Mouse News Lett 40: 29, 1969.

  70. Disteche, C.M., Tantravahi, U., Gandy, S., Eisenhard, M., Adler, D., and Kunkel, L.M.: Isolation and characterization of two repetitive DNA fragments located near the centromere of the mouse X Chromosome.Cytogenet Cell Genet 39: 262–268, 1985.

  71. Do, M.S. and Lonai, P.: Gene organization of murine homeoboxcontaining gene clusters.Genomics 3: 195–200, 1988.

  72. Dobrovolskaia-Zavadskaia, N.: L'irradiation des testicules et l'hérédité chez la souris.Archives Biol 38: 457–501, 1928.

  73. Edwards, Y.H., Parkar, M., Povey, S., West, L.F., Parrington, J.M., and Solomon, E.: Human myosin heavy chain genes assigned to chromosome 17 using a human cDNA clone as probe.Ann Hum Genet 49: 101–109, 1985.

  74. Eiberg, H., Moller, N., Mohr, J., and Nielsen, L.S.: Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22.Clin Genet 29: 354–359, 1986.

  75. Eicher, E.M. and Varnum, D.: Allelism ofDen andRe.Mouse News Lett 75: 29, 1986.

  76. Eicher, E.M. and Lee, B.K.: The NXSM recombinant inbred strains of mice: Genetic profile for 58 loci including theMtv proviral loci.Genetics 125: 431–446, 1990.

  77. Elliott, R.W., Lee, B.K., and Eicher, E.M.: Localization of the growth hormone gene to the distal half of mouse Chromosome 11.Genomics 8: 591–594, 1990.

  78. Elsevier, S.M., Kucherlapati, R.S., Nichols, E.A., Willecke, K., Creagan, R.P., Giles, R.E., McDougall, J.K., and Ruddle, F.H.: Assignment and regional localization of a gene coding for galactokinase to human chromosome 17q21–22.Cytogenet Cell Genet 14:287–289, 1975.

  79. Evans, E.P., Beechey, C.V., and Searle, A.G.:Mouse News Lett 57: 17, 1977.

  80. Evans, E.P., Burtenshaw, M.D., and Lyon, M.F.: A repositioning of the X chromosome breakpoint of T(X;11)38H.Mouse News Lett 77: 147, 1987.

  81. Falconer, D.S.: Linkage of rex with shaker-2 in the house mouse.Heredity 1: 133–135, 1947.

  82. Falconer, D.S.: Two new mutants, “trembler” and “reeler”, with neurological action in the house mouse (Mus musculus L).J Genet 50: 192–201, 1951.

  83. Falconer, D.S. and Sobey, W.R.: The location, of “trembler” in linkage group VII.J Hered 44: 159–160, 1953.

  84. Ferguson, J.M. and Wallace, M.E.:Mouse News Lett 57: 11, 1977.

  85. Ferguson-Smith, A.C. and Ruddle, F.H.: The genomics of human homeobox-containing loci.Pathol Immunopathol Res 7: 119–126, 1988.

  86. Fisher, R.A., Lyon, M.F., and Owen, A.R.G.: The sex chromosomes in the house mouse.Heredity 1: 355–366, 1947.

  87. Flanagan, S.P.: “Nude” a new hairless gene with pleiotropic effects in the mouse.Genet Res 8: 294–309, 1966.

  88. 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, 1989a.

  89. 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 viral restriction locusFv-1.J Virol 63: 1763–1774, 1989b.

  90. Frankel, W.N., Stoye, J.P., Taylor, B.A., and Coffin, J.M.: A linkage map of endogenous murine leukemia proviruses.Genetics 124: 221–236, 1990.

  91. Frankel, W.N., Coffin, J.M., Cote, M., Seyfried, T.N., Rise, M., Rajan, T.V., Nelson, F.K., Selsing, E., and Gerstein, R.: Backcross data for endogenousMpmv, Pmv, andXmv proviruses.Mouse Genome 89, in press, 1991.

  92. Frater-Schroder, M., Haller, O., Gmur, R., Kierat L., and Anastasi, S.: Allelic forms of mouse transcobalamin 2.Biochem Genet 20: 1001–1014, 1982.

  93. Frater-Schroder, M., Prochazka, M., Haller, O., Arwert, F., Porck, H.J., Skow, L.C., Lundin, L.G., Hilkens, J., and Hilgers, J.: Localization of the gene for the vitamin B12 binding protein transcobalamin II, near the centromere on mouse Chromosome 11, linked with the hemoglobin α-chain locus.Bichem Genet 23: 139–153, 1985.

  94. Fukushige, S.-I., Matsubara, K.-I., Yoshida, M., Sasaki, M., Suzuki, T., Semba, K., Toyoshima, K., and Yamamoto, T.: Localization of a novel v-erbB-related gene, c-erbB-2, on human chromosome 17 and its amplification in a gastric cancer cell line.Mol Cell Biol 6: 955–958, 1986.

  95. George, D.L., Phillips, J.A., III, Francke, U., and Seeburg, P.H.: The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21-to-qter.Hum Genet 57: 138–141, 1981.

  96. Goldgar, D.E., Green, P., Parry, D.M., and Mulvihill, J.J.: Multipoint linkage analysis in neurofibromatosis type 1: An international collaboration.Am J Hum Genet 44: 6–12, 1989.

  97. Goldman, D. and Pikus, H.J.: Fourteen genetically variant proteins of mouse brain: Discovery of two new variants and chromosomal mapping of four loci.Biochem Genet 24: 183–194, 1986.

  98. Gough, N.M., Gough, J., Metcalf, D., Kelso, A., Grail, D., Nicola, N.A., Burgess, A.W., and Dunn, A.R.: Molecular cloning of cDNA encoding a murine haematopoietic growth regulator, granulocyte-macrophage colony stimulating factor.Nature 309: 763–767, 1984.

  99. Graham, A., Papalopulu, N., and Krumlauf, R.: The murine andDrosophila homeobox gene complexes have common features of organization and expression.Cell 57: 367–378, 1989.

  100. Green, E.L.: Shambling, a neurological mutant of the mouse.J Heredity 58: 65–68, 1967.

  101. Green, E.L.: Linkage of shambling with rex in linkage group VII of the mouse.J Hered 59, 1968.

  102. Gropp, A., Tettenborn, U., and von Lehmann, E.: Chromosomenuntersuchungen bei der Tabakmaus (M. poschiavinus) und bei Tabakmaus-Hybriden.Experientia 25: 875–876, 1969.

  103. Gropp, A., Tettenborn, U., and von Lehmann, E.: Chromosomen-variationen vom Robertson'schen Typus bei der Tabakmaus,M. poschiavinus, und ihren Hybriden mit der Laboratoriumsmaus.Cytogenetics 9: 9–23, 1970.

  104. Gropp, A., Winking, H., Zech, L., and Müller, H.: Robertsonian chromosomal variation and identification of metacentric chromosomes in feral mice.Chromosoma 39: 265–288, 1972.

  105. Gropp, A., Kolbus, U., and Giers, D.: Systematic approach to the study of trisomy in the mouse.Cytogenet Cell Genet 14: 42–62, 1975.

  106. Gropp, A.:Mouse News Lett 57: 27–28, 1977.

  107. Guénet, J.-L. and Changeux, J.P.: Acetylcholine receptor symbol changes.Mouse News Lett 80: 5, 1988.

  108. Guénet, J.-L.: Personal communication. Fourth International Workshop for Mouse Genome Mapping, Annapolis MD, 1990.

  109. Gusella, J.F., Gibbons, K., Hobbs, W. Heft, R., Anderson, M., Rashtchian, R., Folstein, S., Wallace, P., Conneally, P.M., and Tanzi, R.: Abstract: TheG8 locus linked to Huntington's disease.Am J Hum Genet 36: 139S, 1984.

  110. Harper, M.E., Barrera-Saldana, H.A., and Saunders, G.F.: Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22–24.Am J Hum Genet 34: 227–234, 1982.

  111. Hart, C.P., Dalton, D.K., Nichols, L., Hunihan, L., Roderick, T.H., Langley, S.H., Taylor, B.A., and Ruddle, F.H.: TheHox-2 homeobox gene complex on mouse Chromosome 11 is closely linked toRe.Genetics 118: 319–327, 1988.

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

  113. Henry, E.W., Cowens, J.S., and Sidman, R.L.: Comparison of trembler and trembler-J mouse phenotypes: Varying severity of peripheral hypomyelination.J Neuropath Exp Neurol 42: 688–706, 1983.

  114. Heston, W.E.: A relationship between susceptibility to induced pulmonary tumors and certain known genes in mice.J Natl Cancer Inst 2: 127–132, 1941.

  115. Heston, W.E.: The “vestigial tail” mouse.J Heredity, 42: 71–74, 1951.

  116. Hilgers, J. and Poort-Keesom, R.: Strain distribution of genetic polymorphisms between BALB/cHeA and STS/A strains.Mouse News Lett 76: 14–26, 1986.

  117. Hoggan, M.D., O'Neill, R.R., and Kozak, C.A.: Nonecotropic murine leukemia viruses in BALB/c and NFS/N mice: Characterization of the BALB/cBxv-1 provirus and the single NFS endogenous xenotrope.J Virol 60: 980–986, 1986.

  118. Holmes, R.S., Popp, R.A., and VandeBerg, J.L.: Genetics of ocular NAD〈+〉-dependent alcohol dehydrogenase in the mouse: Evidence for genetic identity with stomach isozymes and localization ofAhd-4 on Chromosome 11 near, trembler.Biochem Genet 26: 191–205, 1988.

  119. Holmes, R.S. and Rout, U.K.: Distribution ofAhd-4 variants among mouse strains.Mouse News Lett 81: 53, 1988.

  120. Hozier, J., Applegate, M., deVassal, N., and Sawyer, J.: Localization of the cytoplasmic thymidine kinase gene (Tk-1) on mouse Chromosome 11 by in situ molecular hybridization and comparison of human and mouse mapping sites at high cytogenetic resolution.Cytogenet Cell Genet 46: 631, 1987.

  121. Hsieh, C.-L., Birnbaum, M.J., and Francke, U.: Abstract: Assignment of glucose transporter genes to mouse chromosomes 4 (Glut-1) and 11 (Glut-4). Fourth International Workshop for Mouse Genome Mapping, Annapolis MD, 1990a.

  122. Hsieh, C.L., Cheng-Deutsch, A., Gloor, S., Schachner, M., and Francke, U.: Assignment ofAmog (adhesion molecule on glia) gene to mouse Chromosome 11 nearZfp-3 andAsgr-1,2 and to human Chromosome 17.Som Cell Mol Genet 16: 401–405, 1990b.

  123. Huebner, K., Isobe, M., Croce, C.M., Golde, D.W., Kaufman, S.E., and Gasson, J.C.: The human gene encodingGM-CSF is at 5q21–q32, the chromosome region deleted in the 5q- anomaly.Science 230: 1282–1285, 1985.

  124. Huebner, K., Isobe, M., Chao, M., Bothwell, M., Ross, A.H., Finan, J., Hoxie, J.A., Sehgal, A., Buck, C.R., Lanahan, A., Nowell, P.C., Koprowski, H., and Croce, C.M.: The nerve growth factor receptor gene is at human chromosome region 17q12–17q22, distal to the chromosome 17 breakpoint in acute leukemias.Proc Natl Acad Sci USA 83: 1403–1407, 1986.

  125. Heubner, K., Nagarajan, L., Besa, E., Angert, E., Lange, B.J., Cannizzaro, L.A., van den Berghe, H., Santoli, D., Finan, J., Croce, C.M., and Nowell, P.C.: Order of genes on human chromosome 5q with respect to 5q interstitial deletions.Am J Hum Genet 46: 26–36, 1990.

  126. Huerre, C., Junien, C., Weil, D., Chu, M.-L., Morabito, M., Van Cong, N., Myers, J.C., Foubert, C., Gross, M.-S., Prockop, D.J., Boue, A., Kaplan, J.-C., de la Chapelle, A., and Ramirez, F.: Human type I procollagen genes are located on different chromosomes.Proc Natl Acad Sci USA 79: 6627–6630, 1982.

  127. Ihle, J.N., Silver, J., and Kozak, C.A.: Genetic mapping of the mouse interleukin 3 gene to Chromosome 11.J Immunol 138: 3051–3054, 1987.

  128. Irving, S.G., Zipfel, P.F., Balke, J., McBride, O.W., Morton, C.C., Burd, P.R., Siebenlist, U., and Kelly, K.: Two inflammatory mediator cytokine genes are closely linked and variably amplified on chromosome 17q.Nucl Acids Res 18: 3261–3270, 1990.

  129. Isobe, M., Emanuel, B.S., Givol, D., Oren, M., and Croce, C.M.: Localization of gene for human p53 tumour antigen to band 17p13.Nature 320: 84–85, 1986.

  130. Jackson-Grusby, L.L., Pravtcheva, D., Ruddle, F.H., and Linzer, D.I.H.: Chromosomal mapping of the prolactin/growth hormone family in the mouse.Endocrinology 122: 2462–2466, 1988.

  131. Jackson, I.: An anonymous cDNA clone maps to the distal tip of Chromosome 11.Mouse Genome 86: 226, 1990.

  132. Jaenisch, R., Jahner, D., Nobis, P., Simon, I., Lohler, J., Harbers, K., and Grotkopp, D.: Chromosomal position and activation of retroviral genomes inserted into the germ line of mice.Cell 24: 519–529, 1981.

  133. Jenkins, N.A., Copeland, N.G., Taylor, B.A., and Lee, B.K.: Dilute (d) coat colour mutation in DBA/2J mice is associated with the site of integration of an ecotropic MuLV, genome.Nature 293: 370–374, 1981.

  134. Jenkins, N.A., Copeland, N.G., Taylor, B.A., and Lee, B.K.: Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes ofMus musculus.J Virol 43: 26–36, 1982.

  135. Jhanwar, S.C., Chaganti, R.S.K., and Croce, C.M.: Germ-line chromosomal localization of human c-erb-A oncogene.Som Cell Mol Genet 11: 99–102, 1985.

  136. Joseph, D.R., Adamson, M.C., and Kozak, C.A.: Genetic mapping of the gene for androgen-binding protein/sex hormone-binding globulin to mouse chromosome 11.Cytogenet Cell Genet in press, 1991.

  137. Joyner, A.L., Lebo, R.V., Kan, Y.W., Tjian, R., Cox, D.R., and Martin, G.R.: Comparative chromosome mapping of a conserved homoeobbox region in mouse and human.Nature 314: 173–175, 1985.

  138. Kanda, N., Fukushige, S., Murotsu, T., Yoshida, M.C., Tsuchiya, M., Asano, S., Kaziro, Y., and Nagata, S.: Human gene coding for granulocyte-colony stimulating factor assigned to the q21–q22 region of chromosome 17.Som Cell Mol Genet 13: 679–684, 1987.

  139. Kaneko, Y., Homma, C., Maseki, N., Sakurai, M., Toyoshima, K., and Yamamoto, T.: Human c-erbB-2 remains on chromosome 17 in band q21 in the 15, 17 translocation associated with acute promyelocytic leukemia.Jpn J Cancer Res 78: 16–19, 1987.

  140. Keeler, C.E.: A second rexoid coat character in the house mouse.J Heredity 26: 189–191, 1935.

  141. Keir, W.J., Kozak, C.A., Chakraborti, A., Deitrich, R.A., and Sikela, J.M.: The cDNA sequence and chromosomal location of the murine GABA>A<α1 receptor, gene.Genomics 9: 390–395, 1991.

  142. Kelton, D.E., and Rauch, H.: Linkage of open eyelids with linkage group VII of the mouse.J Hered 59: 27–28, 1968.

  143. Killary, A.M., and Fournier, R.E.K.: A genetic analysis of extinction: Transdominant loci regulate expression of liver-specific traits in hepatoma hybrid cells.Cell 38: 523–534, 1984.

  144. Kirk, K.M. and Searle, A.G.: Phenotypic consequences of chromosome imbalance in the mouse.In A. Daniael, (ed.);The Cytogenetics of Mammalian Autosomal Rearrangements, pp. 739–768, Alan Liss, New York, 1988.

  145. Klobutcher, L.A. and Ruddle, F.H.: Phenotype stabilisation and integration of transferred material in chromosome-mediated gene transfer.Nature 280: 657–660 1979.

  146. Koeffler, H.P., Sparkes, R.S., Stang, H., and Mohandas, T.: Regional assignment of genes for human α-globin and phosphoglycollate phosphatase to the short arm of chromosome 16.Proc Natl Acad Sci USA 78: 7015–7018, 1981.

  147. Kola, I., Davey, A., and Gough, N.M.: Localization of the murine leukemia inhibitor factor gene near the centromere on, Chromosome 11.Growth Factors 2: 235–240, 1990.

  148. Kondo, I. and Shimizu, N.: Mapping of the human gene for epidermal growth factor receptor (EGFR) on the p13–p22 region of chromosome 7.Cytogenet Cell Genet 35: 9–14, 1983.

  149. Kozak, C.A. and Ruddle, F.H.: Assignment of the genes for thymidine kinase and galactokinase toMus musculus Chromosome 11 and the preferential segregation of this chromosome in Chinese hamster mouse somatic cell hybrids.Som Cell Genet 3: 121–133, 1977.

  150. Kozak, C.A. and Rowe, W.P.: Genetic mapping of ecotropic murine leukemia virus-inducing loci in six inbrid strains.J Exp Med 155: 524–534, 1982.

  151. Kozak, C., Danciger, M., and Farber, D.: Abstract: Chromosome assignment in the mouse of the genes for several proteins involved in visual transduction.Cytogenet Cell Genet 51: 1025, 1989.

  152. Kucherlapati, R., McDougall, J.K., and Ruddle, F.H.: Regional localization of the human genes for thymidine kinase, lactate dehydrogenase-A and esterase-A4.Cytogenet Cell Genet 13: 108–110, 1974.

  153. Landegent, J.E., Jansen in de Wal, N., Fisser-Groen, Y.M., Bakker, E., van der Ploeg, M., and Pearson, P.L.: Fine mapping of the Huntington disease linkedD4S10 locus by non-radioactive in situ hybridization.Hum Genet 73: 354–357, 1986.

  154. Lane, P.W.:tn. Mouse News Lett 37: 34, 1967.

  155. Lane, P.W.: Vibrator,vb. Mouse News Lett 50: 44, 1974.

  156. Lane, P.W.: Linkage; Chrs 1, 2, 4, 6, 10, 11, 14, 16, X. Personal communication, 1982.

  157. Lane, P.W., Ganser, A.L., Kerner, A.L., and White, W.F.: Spasmodic, a mutation on Chromosome 11 in the mouse.J Hered 78: 353–356, 1987.

  158. Law, M.L., Cai, G.-Y., Hartz, J., Kao, F.-T., Hogg, D., Breitman, M.L., and Tsui, L.-C.: Localization of a β-crystallin, gene,Hu-β-A3/A1 (gene symbol:CRYB1), to the long arm of human chromosome 17.Cytogenet Cell Genet 42: 202–207, 1986.

  159. Le Beau, M.M., Westbrook, C.A., Diaz, M.O., Rowley, J.D., and Oren, M.: Translocation of the p53 gene in t(15,17) in acute promyelocytic leukemia.Nature 316: 826–828, 1985.

  160. Le Beau, M.M., Westbrook, C.A., Diaz, M.O., Larson, R.A., Rowley, J.D., Gasson, J.C., Golde, D.W., and Sherr, C.J.: Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders.Science 231: 984–987, 1986.

  161. Le Beau, M.M., Epstein, N.D., O'Brien, S.J., Nienhuis, A.W., Yang, Y.-C., Clark, S.C., and Rowley, J.D.: The interleukin 3 gene is located on human chromosome 5 and is, deleted in myeloid leukemias with a deletion of 5q.Proc Natl Acad Sci USA 84: 5913–5917, 1987a.

  162. Le Beau, M.M., Lemons, R.S., Carrino, J.J., Pettenati, M.J., Souza, L.M., Diaz, M.O., and Rowley, J.D.: Chromosomal localization of the human G-CSF gene to 17q11 proximal to the breakpoint of the t(15,17) in acute promyelocytic leukemia.Leukemia 1: 795–799, 1987b.

  163. Ledbetter, D.H., Ledbetter, S.A., vanTuinen, P., Summers, K.M., Robinson, T.J., Nakamura, Y., Wolff, R., White, R., Barker, D.F., Wallace, M.R., Collins, F.S., and Dobyns, W.B.: Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated “island” in the Miller-Dieker chrormosome region.Proc Natl Acad Sci USA 86: 5136–5140, 1989.

  164. Lee, J.S. and Young, I.G.: Fine-structure mapping of the murineIL-3 and GM-CSF genes by pulsed-field gel electrophoresis and molecular cloning.Genomics 5: 359–362, 1989.

  165. Lee, J.S., Campbell, H.D., Kozak, C.A., and Young, I.G.: TheIl-4 andIl-5 genes are closely linked and are part of a cytokine gene cluster on mouse Chromosome 11.Som Cell Mol Genet 15: 143–152, 1989.

  166. Leinwand, L.A., Fournier, R.E.K., Nadel-Ginard, B., and Shows, T.B.: Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: Localization on a single chromosome.Science 221: 766–768, 1983.

  167. Levine, M., Rubin, G.M., and Tjian, R.: Human DNA sequences homologous to a protein coding region conserved between homeotic genes ofDrosophila.Cell 38: 667–673, 1984.

  168. Lonai, P., Arman, E., Czosnek, H., Ruddle, F.R., and Blatt, C.: New murine homeoboxes: Structure, chromosomal assignment, and differential expression in adult erythropoiesis.DNA 6: 409–418, 1987.

  169. Love, J.M., Knight, A.M., McAlleer, M.A., and Todd, J.A.: Toward construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites.Nucl. Acid Res 18: 4123–4130, 1990.

  170. Lyon, M.F., Mason, I.M., and Bigger, T.R.L.:Mouse News Lett 56: 37, 1977.

  171. Lyon, M.F. and Glenister, P.H.: Bareskin (Bsk).Mouse News Lett 71: 26, 1984.

  172. Lyon, M.F. and Glenister, P.H.: Chylous ascites (Chy) on Chromosome 11.Mouse News Lett 72: 106–107, 1985.

  173. Lyon, M.F. and Glenister, P.H.: Gene order ofChy-vt-Re on Chromosome 11.Mouse News Lett 74: 96, 1986.

  174. Lyon, M.F. and Zenthon, J.F.: Close linkage of bareskin (Bsk) and rex (Re).Mouse News Lett 74: 96, 1986.

  175. Mackensen, J.S.: “Open eyelids” in newborn mice.J Heredity 51: 188–190, 1960.

  176. Magenis, E., Gusella, J., Weliky, K., Haight, G., and Sheehy, B.: Abstract: Huntington disease-linked (HD) restriction fragment polymorphism localized to band p16 of chromosome 4 by in situ hybridization.Cytogenet Cell Genet 40: 685, 1985.

  177. Magenis, R.E., Gusella, J., Weliky, K., Olson, S., Haight, G., Toth-Fejel, S., and Sheehy, R.: Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization.Am J Hum Genet 39: 383–391, 1986.

  178. Malo, D., Schurr, E., Levenson, R., and Gros, P.: Assignment of Na,K-ATPase β<2<-subunit gene (Atpb-2) to mouse Chromosome 11.Genomics 6: 697–699, 1990.

  179. Manfioletti, G., Ruaro, M.E., Del Sal, G., Philipson, L., and Schneider, C.: A growth arrest-specific (gas) gene codes for a membrane protein.Mol Cell Biol 10: 2924–2930, 1990.

  180. Mason, I.J., Murphy, D., Munke, M., Francke, U., Elliott, R.W., and Hogan, B.L.M.: Developmental and transformation-sensitive expression of theSparc gene on mouse Chromosome 11.EMBO J 5: 1831–1837, 1986.

  181. Mather, P.B. and Holmes, R.S.: Biochemical genetics of aldehyde dehydrogenase isozymes in the mouse: Evidence for stomach-and testis-specific isozymes.Biochem Genet 22: 981–995, 1985.

  182. Mattei, M.G., Dautigny, A., Pham-Dinh, D., Passage, E., Mattei, J.F., and Jolles, P.: The gene encoding the large human neurofilament subunit (NF-H) maps to the q12.1–q13.1 region on human chromosome 22.Hum Genet 80: 293–295, 1988.

  183. Mattei, M.G., Passage, E., Mattei, J.F., Dautigny, A., Pham-Dinh, D., and Jolles, P.: Localization of the gene coding for the large mouse neurofilament subunitNfh.Mouse News Lett 84: 96, 1989.

  184. Mazan, S. and Bachellerie, J.P.: Structure and organization of mouse U3B RNA functional genes.J Biol Chem 263: 19461–19467, 1988.

  185. Mazan, S. and Bachellerie, J.P.: Organization of the gene family encoding mouse U3B RNA: Role of gene conversions in its concerted evolution.Gene 94: 263–272, 1990.

  186. Mazan, S., Mattei, M.G., Passage, E., and Bachellerie, J.P.: Composition and chromosomal localization of the small multigene family encoding mouse U3B nucleolar RNA.Cytogenet Cell Genet, in press, 1991.

  187. McAleer, M.A. and Todd, J.: Personal communication. Fourth International Workshop for Mouse Genome Mapping, Annapolis MD, 1990.

  188. McBride, O.W., Merry, D. and Givol, D.: The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13).Proc Natl Acad Sci USA 83: 130–134, 1986.

  189. McMahon, A.P. and Bradley, A.: TheWnt-1 (Int-1) proto-oncogene is required for development of a large region of the mouse brain.Cell 62: 1073–1085, 1990.

  190. Mehrabian, M., Sparkes, R.S., Mohandas, T., Fogelman, A.M., and Lusis, A.J.: Localization of monocyte chemotactic protein-1 gene (SCYA2) to human chromosome 17q11.2–q21.1.Genomics 9: 200–203, 1991.

  191. Meier, H.: The neuropathy of teetering, a neurological mutation in the mouse.Archives Neurol 16: 59–66, 1967.

  192. Meruelo, D., Rossomando, A., Scandalis, S., d'Eustachio, P., Fournier, R.E.K., Roop, D.R., Saxe, D., Blatt, C., and Nesbitt, M.N.: Assignment of theLy-6-Ril-1-Sis-H-30-Pol5/Xmmv-72-Ins-3-Krt-1-Int-1-Gdc-1 region to murine chromosome 15.Immunogenetics 25: 361–372, 1987.

  193. Metcalf, D.: The granulocyte-macrophage colony stimulating factors.Cell 43: 5–6, 1985.

  194. Michael, S.K., Hilgers, J., Kozak, C., Whitney, J.B., III, and Howard, E.F.: Characterization and mapping of DNA sequence homologous to mouse U1a1 snRNA: Localization on Chromosome 11 near theDlb-1 andRe loci.Som Cell Mol Genet 12: 215–223, 1986.

  195. Michie, D.: Genetical studies with “vestigial tail” mice. I. The sex difference in crossing-over between vestigial and rex.J Genet 53: 270–279, 1955a.

  196. Michie, D.: Genetical studies with “vestigial tail” mice. II. The position of vestigial in the seventh linkage group.J Genet 53: 280–284, 1955b.

  197. Migeon, B.R. and Miller, C.S.: Human-mouse somatic cell hybrids with single human chromosome (group E): Link with thymidine kinase activity.Science 162: 1005–1006, 1968.

  198. Miki, T., Murphy, P.D., Pletcher, B.A., Kidd, J.R., Ferguson-Smith, A.C., Ruddle, F.H., and Kidd, K.K.: Abstract:HOX2 maps to 17q nearPPY andNGFR.Cytogenet Cell Genet 46: 662, 1987.

  199. Miller, O.J., Allderdice, P.W., and Miller, D.A.: Human thymidine kinase gene locus: Assignment to chromosome 17 in a hybrid of man and mouse cells.Science 173: 244–245, 1971.

  200. Miller, C., Mohandas, T., Wolf, D., Prokocimer, M., Rotter, V., and Koeffler, H.P.: Human p53 gene localized to short arm of chromosome 17.Nature 319: 783–784, 1986.

  201. Miller, M.D., Wilson, S.D., Dorf, M.E., Seuanez, H.N., O'Brien, S.J., and Krangel, M.S.: Sequence and chromosomal location of the I-309 gene: Relationship to genes encoding a family of inflammatory cytokines.J Immunol 145: 2737–2744, 1990.

  202. Mishkin, J.D., Taylor, B.A., and Mellman, W.J.:Glk: A locus controlling galactokinase activity in the mouse.Biochem Genet 14: 637–640, 1976.

  203. Mitelman, F., Manolov, G., Manolova, Y., Billstrom, R., Heim, S., Kristoffersson, U., Mandahl, N., Ferro, M.T., and San Roman, C.: High resolution chromosome analysis of constitutional and acquired t(15,17) maps c-erbA to subband 17q11.2.Cancer Genet Cytogenet 22:95–98, 1986.

  204. Miyatake, S., Otsuka, T., Yokota, T., Lee, F., and Arai, K.: Structure of the chromosomal gene for granulocyte-macrophage colony stimulating factor: comparison of the mouse and human genes.EMBO J 4: 2561–2568, 1985a.

  205. Miyatake, S., Yokota, T., Lee, F., and Arai, K.I.: Structure of the chromosomal gene for murine interleukin 3.Proc Natl Acad Sci USA 82: 316–320, 1985b.

  206. Moore, S.K., Kozak, C., Robinson, E.A., Ullrich, S.J., and Appella, E.: Murine 86 and 84 kDa heat shock proteins, cDNA sequences, chromosome assignments and evolutionary origins.J Biol Chem 264: 5343–5351, 1989.

  207. Morgan, W.C.: A new tail-short mutation in the mouse.J Heredity 41: 208–215, 1950.

  208. Munke, M., Harbers, K., Jaenisch, R., and Francke, U.: Chromosomal mapping of four different integration sites of Moloney murine leukemia virus including the locus for α1(I) collagen in mouse.Cytogenet Cell Genet 43: 140–149, 1986a.

  209. Munke, M., Cox, D.R., Jackson, I.J., Hogan, B.L.M., and Francke, U.: The murineHox-2 cluster of homeo box containing genes maps distal on Chromosome 11 near the tail-short (Ts) locus.Cytogenet Cell Genet 42: 236–240, 1986b.

  210. Munke, M. and Francke, U.: The physical map ofMus musculus Chromosome 11 reveals evolutionary relationships with different syntenic groups of genes inHomo sapiens.J Mol Evol 25: 134–140, 1987.

  211. Nadeau, J.H.: Maps of linkage and synteny homologies between mouse and man.Trends Genet 5: 82–86, 1989.

  212. Nadeau, J.H., Berger, F.G., Cox, D.R., Crosby, J.L., Davisson, M.T., Ferrara, D., Fuchs, C., Hart, E., Hunihan, L., Lalley, P.A., Langley, S.H., Martin, G.R., Nichols, L., Phillips, S.J., Roderick, T.H., Roop, D.R., Ruddle, F.H., Skow, L.C., and Compton, J.G.: A family of type I keratin genes and the homeobox-2 gene complex are closely linked to theRex locus on mouse Chromosome 11.Genomics 5: 454–462, 1989.

  213. Nadeau, J.H., Birkenmeier, C.S., Chowdhury, K., Crosby, J.L., and Lalley, P.A., Zinc finger protein gene complexes on mouse Chromosomes 8 and 11.Genomics 8: 469–476, 1990.

  214. Nasrat, G.E.: Estimation of the recombination fraction between the two linked genesRe andsh-2 in the house mouse when the female is the heterozygous parent.Proc Zool Soc (Bengal) 9: 85–87, 1956.

  215. Neumann, P., Hayes, L.A., and Sidman, R.L.: Linkage data: Cerebellar outflow degeneration (cod).Mouse News Lett 80: 162, 1988.

  216. Nusse, R., de Moes, J., Hilkens, J., and van Nie, R.: Localization of a gene for expression of mouse mammary tumor virus antigens in the GR/Mtv-2〈-〉 mouse strain.J Exp Med 152: 712–719, 1980.

  217. Nusse, R., Brown, A., Papkoff, J., Scambler, P., Shackleford, G., McMahon, A., Moon, R., and Varmus, H.: Establishment ofWnt-series and substitution for certain members of theInt-series.Cell, in press, 1991.

  218. O'Connell, P., Viskochil, D., Buchberg, A.M., Fountain, J., Cawthon, R.M., Culver, M., Stevens, J., Rich, D.C., Ledbetter, D.H., Wallace, M., Carey, J.C., Jenkins, N.A., Copeland, N.G., Collins, F.S., and White, R.: The human homolog of murineEvi-2 lies between two von Recklinghausen neurofibromatosis translocations.Genomics 7: 547–554, 1990.

  219. Owerbach, D., Rutter, W.J., Martial, J.A., Baxter, J.D., and Shows, T.B.: Genes for growth hormone, chorionic somatomammotropin and growth hormone-like genes on chromosome 17 in humans.Science 209: 289–292, 1980.

  220. Pagliusi, S., Antonicek, H., Gloor, S., Frank, R., Moos, M., and Schachner, M., Identification of a cDNA clone specific for the neural cell adhesion moleculeAMOG.J Neurosci Res 22: 113–119, 1989.

  221. Pajunen, L., Myllyla, R., Helaakoski, T., Pihlajaniemi, T., Tasanen, K., Hoyhtya, M., Tryggvason, K., Solomon, E., and Kivirikko, K.I.: Assignment of the gene coding for both the β-subunit of prolyl 4-hydroxylase and the enzyme disulfide isomerase to human chromosome region 17p11-qter.Cytogenet Cell Genet 47: 37–41, 1988.

  222. Peters, J. and Nash, H.R.: Esterases ofMus musculus: Substrate and inhibition characteristics, new isozymes, and homologies with man.Biochem Genet 16: 553–569, 1978.

  223. Peterson, A. and Biddle, F.: Cocked,co.Mouse News Lett 43: 19, 1970.

  224. Peterson, T.C., Killary, A.M., and Fournier, R.E.K.: Chromosomal assignment andtrans regulation of the tyrosine aminotransferase structural gene in hepatoma hybrid cells.Mol Cell Biol 5: 2491–2494, 1985.

  225. Pettenati, M.J., Le Beau, M.M., Lemons, R.S., Shima, E.A., Kawasaki, E.S., Larson, R.A., Sherr, C.J., Diaz, M.O., and Rowley, J.D.: Assignment ofCSF-1 to 5q33.1: Evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders.Proc Natl Acad Sci USA 84: 2970–2974, 1987.

  226. Ponder, B.A.J., Festing, M.F.W., and Wilkinson, M.M.: An allelic difference determines reciprocal patterns of expression of binding sites for Dolichos biflorus lectin in inbred strains of mice.J Embryol Exp Morphol 87: 229–239, 1985.

  227. Popescu, N.C., Cheng, S., and Pastan, I., Chromosomal localization of the gene for a human thyroid hormone-binding protein.Am J Hum Genet 42: 560–564, 1988.

  228. Popescu, N.C., King, C.R., and Kraus, M.H.: Localization of the humanerbB-2 gene on normal and rearranged chromosomes 17 to bands q12–21.32.Genomics 4: 362–366, 1989.

  229. Popp, R.A.: Studies on the mouse hemoglobin loci. II, III, IV.J Heredity 53: 73–80, 1962.

  230. Popp, R.A.: Inheritance of an erythrocyte and kidney esterase in the mouse.J Heredity 57: 197–201, 1966.

  231. Pravtcheva, D., Rabin, M., Bartolomei, M., Corden, J., and Ruddle, F.H.: Chromosomal assignment of gene encoding the largest subunit of RNA polymerase II in the mouse.Som Cell Mol Genet 12: 523–528, 1986.

  232. Prochazka, M., Gaskins, H.R., and Leiter, E.H.:Emv-30: A novel ecotropic MuLV present in NOD/Lt and NON/Lt strains.Mouse Genome 89, in press, 1991.

  233. Rabin, M., Hart, C.P., Ferguson-Smith, A., McGinnis, W., Levine, M., and Ruddle, F.H.: Two homoeo box loci mapped in evolutionarily related mouse and human chromosomes.Nature 314: 175–178, 1985.

  234. Rappold, G.A. and Vosberg, H.P.: Chromosomal localization of a human myosin heavy-chain gene by in situ hybridization.Hum Genet 65: 195–197, 1983.

  235. Retief, E., Parker, M.I., and Retief, A.E.: Regional chromosome mapping of human collagen genes α 2(I) and α 1(I) (COLIA2 andCOLIA1).Hum Genet 69: 304–308, 1985.

  236. Rettig, W.J., Thomson, T.M., Spengler, B.A., Biedler, J.L., and Old, L.J.: Assignment of human nerve growth factor receptor gene to chromosome 17 and regulation of receptor expression in somatic cell hybrids.Som Cell Mol Genet 12: 441–447, 1986.

  237. Rider, S.H., Gorman, P.A., Shipley, J., Roeling, H., Nusse, R., Xu, W., Sheer, D., and Solomon, E.: Abstract: Localisation of the humanInt-4 (INT4) gene.Cytogenet Cell Genet 51: 1066, 1989.

  238. Robert, B., Barton, P., Minty, A., Daubas, P., Weydert, A., Bonhomme, F., Catalan, J., Chazottes, D., Guénet, J.-L., and Buckingham, M.: Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross.Nature 314: 181–183, 1985.

  239. Robinson, T.J., Morris, D.J., and Ledbetter, D.H.: Chromosomal assignment and regional localization of myeloperoxidase in the mouse.Cytogenet Cell Genet 53: 83–86, 1989.

  240. Roderick, T.H., Hutton, J.J., and Ruddle, F.H.: Linkage of esterase-3 (Es-3) and rex (Re) on linkage group VII of the mouse.J Hered 61: 278–279, 1970.

  241. Roderick, T.H.: Position of jackson shaker.Mouse News Lett 47: 37, 1972.

  242. Roelink, H., Wagenaar, E., Lopes da Silva, S., and Nusse, R.:Wnt-3, a gene activated by proviral insertion in mouse mammary tumors, is homologous toInt-1/Wnt-1 and is normally expressed in mouse embryos and adult brain.Proc Natl Acad Sci USA 87: 4519–4523, 1990.

  243. Romano, V., Bosco, P., Rocchi, M., Costa, G., Leube, R.E., Franke, W.W., and Romeo, G.: Chromosomal assignments of human type I and type II cytokeratin genes to different chromosomes.Cytogenet Cell Genet 48: 148–151, 1988.

  244. Rosenberg, M., RayChaudhury, A., Shows, T.B., Le Beau, M.M., and Fuchs, E.: A group of type I keratin genes on human chromosome 17: Characterization and expression.Mol Cell Biol 8: 722–736, 1988.

  245. Rotter, V., Wolf, D., Pravtcheva, D., and Ruddle, F.H.: Chromosomal assignment of the murine gene encoding the transformation-related protein p53.Mol Cell Biol 4: 382–385, 1984.

  246. Rout, U.K. and Holmes, R.S.: Mapping ofAhd-4 andAhd-6 to Chromosome 11.Mouse News Lett 81: 54, 1988.

  247. Russell, E.S., Blake, S.L., and McFarland, E.C.: Characterization and strain distribution of four alleles at the hemoglobin α-chain structural locus in the mouse.Biochem Genet 7: 313–330, 1972.

  248. Russell, E.S. and McFarland, E.C.: Genetics of mouse hemoglobins.Ann NY Acad Sci 241: 25–38, 1974.

  249. Said, K., Jacquart, T., Montgelard, C., Sonjaya, H., Helal, A.N., and Britton-Davidian, J.: Robertsonian house mouse populations in Tunisia: A karyological and biochemical study.Genetica 68: 151–156, 1986.

  250. Sanford, J.P., Elliott, R.W., and Doyle, D.: Asialoglycoprotein receptor genes are linked on Chromosome 11 in the mouse.DNA 7: 721–728, 1988.

  251. Santisteban, I., Povey, S., West, L.F., Parrington, J.M., and Hopkinson, D.A.: Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase,ALDH3.Ann Hum Genet 49: 87–100, 1985.

  252. Schneider, C., King, R.M., and Philipson, L.: Genes specifically expressed at growth arrest of mammalian cells.Cell 54: 787–793, 1988.

  253. Searle, A.G.: Tipsy, a new mutant in linkage group VII of the mouse.Genet Res 2: 122–126, 1961.

  254. Searle, A.G., Ford, C.E., Evans, C.V., Beechey, M.D., Burtenshaw, M.D., and Clegg, H.M.: The induction of translocations in mouse spermatozoa. I. Kinetics of dose response with acute x-irradiation.Mutat Res 22: 157–174, 1974.

  255. Searle, A.G., Beechey, C.V., Evans, E.P., and Kirk, M.: Two new X-autosome translocations in the mouse.Cytogenet Cell Genet 35: 279–292, 1983.

  256. Seharaseyon, J., Bober, E., Hsieh, C.L., Fodor, W.L., Francke, U., Arnold, H.H., and Vanin, E.F.: Human embryonic/atrial myosin alkali light chain gene: Characterization, sequence and chromosomal location.Genomics 7: 289–293, 1990.

  257. Seizinger, B.R., et al.: Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.Cell 49: 589–594, 1987.

  258. Seldin, M.F.: Personal communication. Fourth International Workshop for Mouse Genome Mapping, Annapolis MD, 1990.

  259. Shimizu, N., Behzadian, M.A., and Shimizu, Y.: Genetics of cell surface receptors for bioactive polypeptides: Binding of epidermal growth factor is associated with the presence of human chromosome 7 in human-mouse cell hybrids.Proc Natl Acad Sci USA 77: 3600–3604, 1980.

  260. Showe, L.C., Ballantine, M., and Huebner, K.: Localization of the gene for the erythroid anion exchange protein, band 3 (EMPB3), to human chromosome 17.Genomics 1: 71–76, 1987.

  261. Shultz, L.D., Bedigian, H.G., Heiniger, H.J., and Eicher, E.M.: The congenitally athymic streaker mouse.Proc Third Intl Workshop Nude Mice: 33–39, 1982.

  262. Shupp Byrne, D.E. and Church, R.L.: Assignment of the genes for the mouse type I procollagen to chromosome 16 using mouse fibroblast-Chinese hamster somatic cell hybrids.Som Cell Genet 9: 313–331, 1983.

  263. Silver, J., Whitney, J.B., III, Kozak, C., Hollis, G., and Kirsch, I.:Erbb is linked to the α-globin locus on mouse Chromosome 11.Mol Cell Biol 5: 1784–1786, 1985.

  264. Simmers, R.N., Smith, J., Shannon, M.F., Wong, G., Lopez, A.F., Baker, E., Sutherland, G.R., and Vadas, M.A.: Localization of the humanG-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia.Hum Genet 78: 134–136, 1988.

  265. Smith, A., Lalley, P.A., Killary, A.M., Ghosh-Choudhury, G., Wang, L.M., Han, E.S., Martinez, L., Naylor, S.L., and Sakaguchi, A.Y.:Sigje, a member of the small inducible gene family that includes platelet factor 4 and melanoma growth stimulatory activity, is on mouse Chromosome 11.Cytogenet Cell Genet 52: 194–196, 1989.

  266. Snell, G.D., and Law, L.W.: A linkage between shaker-2 and wavy-2 in the house mouse.J Hered 30, 447, 1939.

  267. Sparkes, R.S., Mohandas, T., Heinzmann, C., Gorin, M.B., Zollman, S., and Horwitz, J.: Assignment of a human β-crystallin gene to 17cen-q23.Hum Genet 74: 133–136, 1986.

  268. Spurr, N.K., Solomon, E., Jansson, M., Sheer, D., Goodfellow, P.N., Bodmer, W.F., and Vennstrom, B.: Chromosomal localisation of the human homologues to the oncogeneserbA andB.EMBO J 3: 159–163, 1984.

  269. Staats, J.: Standardized nomenclature for inbred strains of mice: Sixth listing.Cancer Res 36: 4333–4377, 1976.

  270. Staats, J.: List of inbred strains.In M.C. Green (ed.);Genetic Variants and Strains of the Laboratory Mouse, Gustav Fischer Verlag, Stuttgart, pp. 373–376, 1981.

  271. Stahl, J., Gearing, D.P., Willson, T.A., Brown, M.A., King, J.A., and Gough, N.M.: Structural organization of the genes for murine and human leukemia inhibitory factor. Evolutionary conservation of coding and non-coding regions.J Biol Chem 265: 8833–8841, 1990.

  272. Steffen, D.L., Taylor, B.A., and Weinberg, R.A., Continuing germ line integration of AKV proviruses during the breeding of AKR mice and derivative recombinant inbred strains.J Virol 42: 165–175, 1982.

  273. Summar, M.L., Phillips, J.A., III, Krishnamani, M.R.S. Keefer, J., Trofatter, J., Schwartz, R.C., Tsipouras, P., Willard, H., and Ullrich, A.: Protein kinase C: A new linkage marker for growth hormone and forCOL1A1.Genomics 5: 163–165, 1989.

  274. Sundar Raj, C.V., Church, R.L., Klobutcher, L.A., and Ruddle, F.H.: Genetics of the connective tissue proteins: Assignment of the gene for human type I procollagen to chromosome 17 by analysis of cell hybrids and microcell hybrids.Proc Natl Acad Sci USA 74: 4444–4448, 1977.

  275. Sutherland, G.R., Baker, E., Callen, D.F., Hyland, V.J., Wong, G., Clark, S., Jones, S.S., Eglinton L.K., Shannon, M.F., Lopez, A.F., and Vadas, M.A.: Interleukin 4 is at 5q31 and interleukin 6 is at 7p15.Hum Genet 79: 335–337, 1988a.

  276. Sutherland, G.R., Baker, E., Callen, D.F., Campbell, H.D., Young, Y.G., Sanderson, C.J., Garson, O.M., Lopez, A.F., and Vadas, M.A.: Interleukin-5 is at 5q31 and is deleted in the 5q- syndrome.Blood 71: 1150–1152, 1988b.

  277. Sutherland, G.R., Baker, E., Hyland, V.J., Callen, D.F., Stahl, J., and Gough, N.M.: The gene for human leukemia inhibitory factor (LIF) maps to 22q12.Leukemia 3: 9–13, 1989.

  278. Swallow, D.M., Turner, V.S., and Hopkinson, D.A.: Isozymes of rodent 5′ nucleotidase: Evidence for two independent structural lociUmph-1 andUmph-2.Ann Hum Genet 47: 9–17, 1983.

  279. Swaroop, A., Hogan, B.L.M., and Francke, U.: Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: Sequence, expression, and localization of the gene to chromosome 5q31–q33.Genomics 2: 37–47, 1988.

  280. Sweet, H.O., Roderick, T.H., and Davisson, M.T.: Linkage of Tail short (Ts).Mouse News Lett 60: 51, 1979.

  281. Sweet, H.O. and Lane, P.W.: Chr 19 and Chr 11 linkages.Mouse News Lett 59: 27, 1979.

  282. Takahashi, M., Yoshida, M.C., Satoh, H., Hilgers, J., Yaoita, Y., and Honjo, T.: Chromosomal mapping of the mouseIL-4 and humanIL-5 genes.Genomics 4: 47–52, 1989.

  283. Taylor, B.A., Rowe, L., Jenkins, N.A., and Copeland, N.G.: Chromosomal assignment of two endogenous ecotropic murine leukemia virus proviruses of the AKR/J mouse strain.J Virol 56: 172–175, 1985.

  284. Taylor, B.A.: RI strain distribution patterns.Mouse News Lett 77: 130, 1987.

  285. Taylor, B.A. and Rowe, L.: A mouse linkage testing stock possessing multiple copies of the endogenous ecotropic murine leukemia virus genome.Genomics 5: 221–232, 1989.

  286. Tsipouras, P., Schwartz, R. C., Phillips, J. A., III, and Willard, H.F.: A centromere-based linkage group on the long arm of human chromosome 17.Cytogenet Cell Genet 47: 109–110, 1988.

  287. Tweardy, D.J., Cannizzaro, L.A., Palumbo, A.P., Shane, S., Huebner, K., van Tuinen, P., Ledbetter, D.H., Finan, J.B., Nowell, P.C., and Rovera, G.: Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiform cell line and localization of theG-CSF gene to chromosome band 17q21.Oncogene Res 1: 209–220, 1987.

  288. Uiterdijk, H.G., Ponder, B.A.J., Festing, M.F.W., Hilgers, J., Skow, L., and Van Nie, R.: The gene controlling the binding sites of Dolichos biflorus agglutinin,Dlb-1, is on Chromosome 11 of the mouse.Genet Res 47: 125–129, 1986.

  289. van Tuinen, P. and Ledbetter, D.H.: Abstract: Construction and utilization of a detailed somatic cell hybrid mapping panel for human chromosome 17: Localization of an anonymous clone to the critical region of Miller-Dieker syndrome, deletion 17q13.Cytogenet Cell Genet 46: 708–709, 1987.

  290. Wainscoat, J.S., Kanavakis, E., Weatherall, D.J., Walker, J., Holmes-Seidle, M., Bobrow, M., and Donnison, A.B.: Regional localisation of the human α-globin genes.Lancet II: 301–302, 1981.

  291. Wallace, M.E. and Ferguson, J.: Linkage for bald-arthritic,Bda.Mouse News Lett 71: 19, 1984.

  292. Wang, H.S., Greenberg, C.R., Kalousek, D., Gusella, J., Horsman, D., and Hayden, M.R.: Abstract: Subregional assignment of the linked markerD4S10 (G8) for Huntington disease by in situ hybridization.Cytogenet Cell Genet 40: 772, 1985.

  293. Wang, H.S., Greenberg, C.R., Hewitt, J., Kalousek, D., and Hayden, M.R.: Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1–16.3.Am J Hum Genet 39: 392–396, 1986.

  294. Watanabe, T., Masaki, S., Takahashi, N., Nishimura, M., and Kato, H.: Restriction fragment length polymorphism and chromosome mapping of a mouse homeo box gene,Hox-2.1.Biochem Genet 26: 805–813, 1988.

  295. Webb, G.C., Lee, J.S., Campbell, H.D., and Young, I.G.: The genes for interleukins 3 and 5 map to the same locus on mouse Chromosome 11.Cytogenet Cell Genet 50: 107–110, 1989.

  296. Weimar, W.R., Lane, P.W., and Sidman, R.L.: “Vibrator” (vb): Autosomal recessive inheritance of spongiform spinocerebellar degeneration in mice.Brain Res 251: 357–364, 1982.

  297. 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 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.

  298. Whitney, J.B., III and Russell, E.S.: Linkage of genes for adult α-globin and embryonic α-like globin chains.Proc Natl Acad Sci USA 77: 1087–1090, 1980.

  299. Wilson, D.E., Swallow, D.M., and Povey, S.: Assignment of the human gene for uridine 5-prime-monophosphate phosphohydrolase (UMPH2) to the long arm of chromosome 17.Ann Hum Genet 50: 223–227, 1986.

  300. Wilson, D.E., Woodard, D., Sandler, A., Erickson, J., and Gurney, A.: Provisional assignment of the gene for uridine monophosphatase-2 (Umph-2) to mouse Chromosome 11.Biochem Genet 25: 1–6, 1987.

  301. Wilson, S.D., Billings, P.R., D'Eustachio, P., Fournier, R.E.K., Geissler, E., Lalley, P.A., Burd, P.R., Housman, D.E., Taylor, B.A., and Dorf, M.E.: Clustering of cytokine genes on mouse Chromosome 11.J Exp Med 171: 1301–1314, 1990.

  302. Winking, H., Dulic, B., and Gropp, A.:Mouse News Lett 60: 55, 1979a.

  303. Winking, H., Noack, G., Gropp, A., and Capanna, E.:Mouse News Lett 60: 55, 1979b.

  304. Wright, M.E.: Two sex-linkages in the house mouse with unusual recombination values.Heredity 1: 349–354, 1947.

  305. Xu, W., Gorman, P.A., Rider, S.H., Hedge, P.J., Moore, G., Prichard, C., Sheer, D., and Solomon, E.: Construction of a genetic map of human chromosome 17 by use of chromosomemediated gene transfer.Proc Natl Acad Sci USA 85: 8563–8567, 1988.

  306. Yang-Feng, T.L., Schechter, A.L., Weinberg, R.A., and Francke, U.: Abstract: Oncogene from rat neuro/glioblastomas (human gene symbolNGL) is located on the proximal long arm of human chromosome 17 andEGFR is confirmed at 7p13–q11.2.Cytogenet Cell Genet 40: 784, 1985.

  307. Yang-Feng, T.L., Ullrich, A., and Francke, U.: Abstract: Protein kinase C genes in mouse:Pkca maps to MMU 11 andPkcc to MMU 7.Cytogenet Cell Genet 46: 723, 1987.

  308. Yang-Feng, T.L., Xue, F., Zhong, W., Cotecchia, S., Frielle, T., Caron, M.G., Lefkowitz, R.J., and Francke, U.: Chromosomal organization of adrenergic receptor genes.Proc Natl Acad Sci USA 87: 1516–1520, 1990.

  309. Zabel, B.U., Fournier, R.E., Lalley, P.A., Naylor, S.L., and Sakaguchi, A.Y.: Cellular homologs of the avian erythroblastosis viruserb-A anderb-B genes are syntenic in mouse but asyntenic in man.Proc Natl Acad Sci USA 81: 4874–4878, 1984.

  310. Zabel, B.U., Naylor, S.L., Sakaguchi, A.Y., and Gusella, J.F.: Mapping of the DNA locusD4S10 and the linked Huntington's disease gene to 4p16-p15.Cytogenet Cell Genet 42: 187–190, 1986.

  311. Zakut-Houri, R., Oren, M., Bienz, B., Lavie, V., Hazum, S., and Givol, D.: A single gene and a pseudogene for the cellular tumor antigen p53.Nature 306: 594–597, 1983.

  312. Zech, L., Evans, E.P., Ford, C.E., and Gropp, A.: Banding patterns in the mitotic chromosomes of tobacco mouse.Exp Cell Res 70: 263–268, 1972.

Download references

Author information

Correspondence to Arthur M. Buchberg.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Buchberg, A.M., Moskow, J.J., Buckwalter, M.S. et al. Mouse chromosome 11. Mammalian Genome 1, S158–S191 (1991).

Download citation


  • Mouse Chromosome