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Publication : Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1.

First Author  Epstein DJ Year  1991
Journal  Genomics Volume  10
Issue  1 Pages  89-93
PubMed ID  2045114 Mgi Jnum  J:11244
Mgi Id  MGI:59683 Doi  10.1016/0888-7543(91)90488-z
Citation  Epstein DJ, et al. (1991) Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1. Genomics 10(1):89-93
abstractText  We have used a set of markers newly assigned to the proximal portion of mouse chromosome 1 to characterize the chromosomal segment deleted in the splotch-retarded (Spr) mouse mutant. Among nine markers tested in the heterozygote Spr/+mouse, we have identified four genes, Vil, Des, Inha, and Akp-3, which map within the Spr deletion. The closest distal marker to the deletion is the Acrg gene, with the distal deletion breakpoint mapping within the 0.8-cM segment separating Akp-3 and Acrg. The most proximal gene to the Spr deletion is Tp1. The proximal deletion breakpoint maps within the 0.8-cM segment separating Tp1 and Vil. The minimum size of the Spr deletion would therefore be limited to 14 cM, the genetic distance between Vil and Akp-3. The maximum size of the Spr deletion is estimated to be 16 cM, the genetic distance between Tp1 and Acrg.
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