Mapping Data

Experiment

• Experiment
  TEXT-Genetic Cross
• Chromosome
  1
• Reference
  J:30570 Peters J, et al., Genetic and phenotypic analysis of Del(1)Sp^r3H and Pax3^Sp-4H. Mouse Genome. 1995;93(4):1041-3
• ID
  MGI:46006

Genes

Gene	Allele	Assay Type
Del(1)3H		visible phenotype
D1Mit19		PCR amplified length variant
D1Mit23		PCR amplified length variant
D1Mit24		PCR amplified length variant
D1Mit46		PCR amplified length variant
Pax3	Pax3^Sp-4H	visible phenotype
D1Mit8		PCR amplified length variant
D1Mit10		PCR amplified length variant
D1Mit26		PCR amplified length variant

Notes

• Experiment
  Del(1)3H, D1Mit19, D1Mit23, D1Mit24, D1Mit46, Pax3, D1Mit8, D1Mit10, D1Mit26.
  The extent of mouse Chromosome 1 deleted in Del(1)3H was analysed in crosses involving C3H/HeH, 101/H and Mus spretus. The deletion is referred to by the authors as Del(1)Sp^r3H and is phenotypically identified by a white spot which results from Pax3 being deleted. DNA from informative Del(1)Sp^r3H/+ mice were tested for polymorphic SSR markers in the region of the deletion. Del(1)3H does not include the proximal marker D1Mit19 or the distal markers D1Mit18, D1Mit10 and D1Mit26. Markers D1Mit23, D1Mit24 and D1Mit46 are included within the deleted region.