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Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV

Published online by Cambridge University Press:  14 April 2009

Mary F. Lyon
Affiliation:
M.R.C. Radiobiology Unit, Harwell, Berkshire
R. Meredith
Affiliation:
M.R.C. Radiobiology Unit, Harwell, Berkshire
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The autosomal recessive gene muted, mu, which arose spontaneously, dilutes coat and eye colour and causes absence of otoliths in some but not all homozygotes. Its locus is in linkage group XIV of the mouse, and the order of loci was shown to be bg–Xt–sa–mu–f–pe.

Type
Short Papers
Copyright
Copyright © Cambridge University Press 1969

References

REFERENCES

Erway, L., Hurley, L. S. & Fraser, A. (1966). Neurological defect: manganese in pheno-copy and prevention of a genetic abnormality of inner ear. Science, N. Y. 152, 17661768.CrossRefGoogle Scholar
Erway, L., Shrader, R. & Hurley, L. S. (1968). Private communication. Mouse News Letter 39, 20.Google Scholar
Lane, P. W. (1965). Private communication. Mouse News Letter 32, 47.Google Scholar
Lyon, M. F. (1951). Hereditary absence of otoliths in the house mouse. J. Physiol., Lond. 114, 110118.CrossRefGoogle ScholarPubMed
Lyon, M. F. (1954). Stage of action of the litter-size effect on absence of otoliths in mice. Z. indukt. Abstamm.- u. VererbLehre 86, 289292.Google Scholar
Lyon, M. F. (1966). Private communication. Mouse News Letter 34, 28.Google Scholar
Lyon, M. F. & Meredith, R. (1965). Private communication. Mouse News Letter 32, 38.Google Scholar
Lyon, M. F., Morris, T., Searle, A. G. & Butler, J. (1967). Occurrences and linkage relations of the mutant ‘extra-toes’ in the mouse. Genet. Res. 9, 383385.CrossRefGoogle ScholarPubMed