Faint lined (Fnl): A novel X-linked coat mutant in the mouse

Genetical Research

Volumn 72, Issue 3, 1998, Pages 211-216

  Gormally, Emmanuelle ^a   Boyd, Yvonne ^a  

^a MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIRTH WEIGHT; CHROMOSOME MARKER; CONTROLLED STUDY; FEMALE; FETUS DEATH; GENE LOCATION; HAPLOTYPE; HETEROZYGOTE; HISTOPATHOLOGY; LETHAL MUTANT; MALE; MOUSE; MOUSE MUTANT; NONHUMAN; SKIN PIGMENTATION; WEANING; X CHROMOSOME LINKAGE;

ANIMALS; CHROMOSOME MAPPING; FEMALE; GENES, LETHAL; GENETIC MARKERS; HAIR; HUMANS; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; MALE; MICE; MICE, INBRED STRAINS; MUTATION; PHENOTYPE; POLYMERASE CHAIN REACTION; SKIN; X CHROMOSOME;

ANIMALIA; MUS SPRETUS; RODENTIA;

EID: 0032443898     PISSN: 00166723     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0016672398003449     Document Type: Article

References (30)

1. Angel, T. A., Faust, C. J., Gonzales, J. C., Kenwrick, S., Lewis, R. A. & Herman, G. E. (1993). Genetic mapping of the X-linked dominant mutations (Str) and bare patches (Bpd) to a 600 kb region of the mouse X chromosome: implications for mapping human disorders in Xq28. Mammalian Genome 4, 171-176.
2. Barber, B. R. (1971). Research news. Mouse News Letter 45, 35.
3. Blaschke, R. J. & Rappold, G. A. (1997). Man to mouse: lessons learnt from the distal end of the human X chromosome. Genome Research 7, 1114-1117.
4. Blair, H. J. & Boyd, Y. (1994). Positioning of 14 simple sequence repeat loci relative to markers on the gene-based map of the mouse X chromosome. Mouse Genome 92, 127-129.
5. Blair, H. J., Gormally, E., Uwechue, I. C. & Boyd, Y. (1998). Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Human Molecular Genetics 7, 549-555.
6. Boyd, Y., Blair, H. J., Cunliffe, P., Denny, P., Gormally, E. & Herman, G. E. (1998). Mouse X chromosome. Mammalian Genome 9, in press.
7. Brockdorff, N., Fisher, E. M. C., Cavanna, J. S., Lyon, M. F. & Brown, S. D. M. (1987). Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses. EMBO J. 6, 3291-3297.
8. Cattanach, B. M., Crocker, A. J. M. & Peters, J. (1984). A further new X-linked gene. Research news. Mouse News Letter 70, 80-81.
9. Cattanach, B. M., Rasberry, C., Evans, E. P., Dandalo, L., Simmler, M. C. & Avner, P. (1991). Genetic and molecular characterisation of an X-chromosome deletion spanning tabby (To) and testicular feminisation (Tfm). Cytogenetics Cell Genetics 56, 137-143.
10. Dietrich, W. F., Miller, J., Steen, R., Merchant, M. A., Damron-Boles, D., Husain, Z., Dredge, R., Daly, M., Ingalls, K. A., O'Connor, T. J., Evans, C. A., De Angelis, M. M., Levinson, D. M., Kruglyak, L., Goodman, N., Copeland, N. G., Jenkins, N. A., Hawkins, T. L., Stein, L., Page, D. C. & Lander, E. S. (1996). A comprehensive genetic map of the mouse genome. Nature 380, 149-152.
11. Ellison, J. W., Salido, E. C. & Shapiro, L. J. (1996). Genetic mapping of the adenine nucleotide translocase-2 gene (Ant2) to the mouse proximal X chromosome. Genomics 36, 369-371.
12. Falconer, D. S. & Isaacson, J. H. (1972). Harlequin and brindled: linkage and differences between coupling and repulsion phenotypes. Mouse News Letter 47, 28.
13. Figuera, L., Pandolfo, M., Dunne, P. W., Cantú, J. M. & Patel, P. I. (1995). Mapping of generalized hypertrichosis locus to chromosome Xq24-q27.1. Nature Genetics 10, 202-207.
14. Glenister, P. H. (1987). Incidence of chromosome anomalies in first cleavage embryos obtained from frozen-thawed mouse embryos fertilized in vitro. Gamete Research 16, 205-216.
15. 2 receptor gene (Agtr2) to the mouse X chromosome. Genomics 30, 369-371.
16. Kidd, A., Carson, L., Gregory, D. W., de Silva, D., Holmes, J., Dean, J. C. S. & Haites, N. (1996). A Scottish family with Bazex-Dupré-Christol syndrome: follicular atrophoderma, congenital hypotrichosis and basal cell carcinoma. Journal of Medical Genetics 33, 493-497.
17. Laval, S. H. & Boyd, Y. (1993). Novel conserved sequences on the mouse and human X chromosomes. Genomics 15, 483-191.
18. Lyon, M. F. (1961). Gene action in the X chromosome of the mouse (Mus musculus L.). Nature 190, 372-373.
19. Lyon, M. F. (1963). Attempts to test the inactive X theory of dosage compensation in mammals. Genetical Research 4, 93-103.
20. Lyon, M. F. (1972). X-chromosome inactivation and developmental patterns in mammals. Biological Reviews 47, 1-35.
21. Ohno, S. (1969). Evolution of sex chromosomes in mammals. Annual Review of Genetics 3, 495-521.
22. Phillips, R. J. S. (1963). Striated, a new sex-linked gene in the house mouse. Genetical Research 4, 151-153.
23. Phillips, R. J. S., Hawker, S. G. & Mosely, H. (1973). Bare patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments. Genetical Research 22, 91-99.
24. Rasberry, C., Beechey, C. & Cattanach, B. M. (1995). Time of death of tattered males. Research news. Mouse Genome 93, 1028.
25. H0). Mammalian Genome 8, 578-580.
26. Sutton, K. A. & Wilkinson, M. F. (1997). The rapidly evolving Pem Homeobox gene and Agtr2, Ant2 and Lamp2 are closely linked in the proximal region of the mouse X chromosome. Genomics 45, 447-450.
27. Uwechue, I. C., Cooper, B. F., Goble, C., Hacker, T., Blair, H. J., Burke, D. T., Herman, G. & Boyd, Y. (1996). The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization. Genomics 37, 238-241.
28. Vabres, P., Lacombe, D., Rabinowitz, L., Aubert, G., Anderson, C. E., Taieb, A., Bonafe, J. L. & HorsCayla, M. C. (1995). The gene for Bazex-Dupré-Christol syndrome maps to chromosome Xq. Journal of Investigative Dermatology 105, 87-91.
29. Yang-Feng, T. L., Degennaro, L. J. & Francke, U. (1986). Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of the human and murine X chromosomes. Proceedings of the National Academy of Sciences of the USA 83, 8679-8683.
30. Zhou, B. K., Boissy, R. E., Pifko-Hirst, S., Moran, D. & Orlow, S. J. (1993). Lysosome-associated membrane protein-1 (LAMP-1) is the melanocyte vesicular membrane glycoprotein band II. Journal of Investigative Dermatology 100, 110-114.