Mapping of Multiple Intestinal Neoplasia ( Min) to Proximal Chromosome 18 of the Mouse
The Min ( multiple intestinal neoplasia) mutation of the mouse has been mapped by analyzing the inheritance of restriction fragment length polymorphisms and simple sequence length polymorphisms in progeny from two intraspecific crosses segregating for the Min mutation. Min , a mutant allele of Apc,...
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Published in | Genomics (San Diego, Calif.) Vol. 15; no. 1; pp. 3 - 8 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
1993
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The
Min (
multiple
intestinal
neoplasia) mutation of the mouse has been mapped by analyzing the inheritance of restriction fragment length polymorphisms and simple sequence length polymorphisms in progeny from two intraspecific crosses segregating for the
Min mutation.
Min , a mutant allele of
Apc, the mouse homolog of the human APC (
adenomatous
polyposis
coli) gene, maps to proximal chromosome 18. The synteny between
Apc and
Mcc, the mouse homolog of the human MCC (
mutated in
colorectal
cancer) gene, is conserved between mouse and human, although the gene order in the
Apc to
Mcc interval is different from that in the APC to MCC interval. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 None |
ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1006/geno.1993.1002 |