Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  2
• Reference
  J:6129 Searle AG, et al., Colinearity in the mouse genome: a study of chromosome 2. Cytogenet Cell Genet. 1979;23(4):255-63
• ID
  MGI:39908

Genes

Gene	Assay Type	Description
T(2;4)1Ca	visible phenotype	G-banding
T(2;4)13H	visible phenotype	G-banding
T(2;6)7Ca	visible phenotype	G-banding
T(2;3)24H	visible phenotype	G-banding
T(2;9)11H	visible phenotype	G-banding
T(2;11)30H	visible phenotype	G-banding
T(2;8)26H	visible phenotype	G-banding
T(1;2)5Ca	visible phenotype	G-banding
T(2;4)1Sn	visible phenotype	G-banding
T(2;16)28H	visible phenotype	G-banding

Notes

• Experiment
  The authors review the genetic and cytogenetic placement of breakpoints on Chromosome 2 for reciprocal translocations T(2;4)1Ca, T(2;4)13H, T(2;6)7Ca, T(2;3)24H, T(2;9)11H, T(2;11)30H, T(2;8)26H, T(1;2)5Ca, T(2;4)1Sn, T(2;16)28H. The placement of these breakpoints agree in their proximal to distal ordering, but there is not good correspondence between the genetic distance and the cytologic distance. The Chromosome 2 breakpoint for T1Ca is localized to band B, T13H to C1, T7Ca to D, T24H to E2, T11H to E4, T30H, T26H and T5Ca to H1, T1Sn to H3 and T28H to H4.