Mapping Data

Experiment

• Experiment
  TEXT-Genetic Cross
• Chromosome
  8
• Reference
  J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
• ID
  MGI:47621

Genes

Gene	Assay Type	Description
D8Mit343	PCR amplified length variant
D8Mit75	PCR amplified length variant
D8Mit102	PCR amplified length variant
D8Mit104	PCR amplified length variant
D8Mit134	PCR amplified length variant
D8Mit135	PCR amplified length variant
D8Mit234	PCR amplified length variant
D8Mit263	PCR amplified length variant
D8Mit306	PCR amplified length variant
D8Mit195	PCR amplified length variant
D8Mit346	PCR amplified length variant
D8Mit236	PCR amplified length variant
D8Mit238	PCR amplified length variant
D8Mit247	PCR amplified length variant
D8Mit264	PCR amplified length variant
D8Mit265	PCR amplified length variant
Cacna1a	Southern analysis	Ccha1a probe1
Lyl1	Southern analysis	Lyl1 cDNA1
Nfix	Southern analysis	Nfix cDNA1
Junb	Southern analysis	Junb cDNA1
Gcdh	Southern analysis	Gcdh cDNA2
D8Mit283	PCR amplified length variant
D8Mit79	PCR amplified length variant
Cbln1	Southern analysis	Cbln1 cDNA2

Notes

• Reference
  Authors state that the mouse tg phenotype is coded by the mouse Chromosome 8 locus Cacna1a.
• Experiment
  The following order of loci was determined in 600 backcross progeny derived from a cross between (B6.D2-tg/tg x CAST/Ei)F1 x B6.D2-tg/tg mice: D8Mit343 - D8Mit75 - D8Mit102 - D8Mit104 - D8Mit134 - D8Mit135 - D8Mit234 - D8Mit263 - D8Mit306 - D8Mit195 - D8Mit346 - D8Mit236 - D8Mit283 - D8Mit247 - D8Mit264 - D8Mit265 - Cacna1a - Lyl1 - Nfix - Junb - Gcdh - D8Mit283 - D8Mit79 - Cbln1. Lyl1 was nonrecombinant with Cacna1a in this cross.