Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  X
• Reference
  J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
• ID
  MGI:1202376

Genes

Gene	Assay Type	Description
DXMit98	PCR amplified length variant
Phex	Southern analysis	CD1
DXMit180	PCR amplified length variant
DXMit179	PCR amplified length variant
DXMit70	PCR amplified length variant
DXMit28	PCR amplified length variant
DXMit33	PCR amplified length variant
DXMit99	PCR amplified length variant
DXMit189	PCR amplified length variant
Rps6ka3	Southern analysis	Rsk2 cDNA
Pdha1	Southern analysis
DXMit220	PCR amplified length variant
DXMit121	PCR amplified length variant
DXMit21	PCR amplified length variant

Notes

• Experiment
  The authors tested DNA prepared from (Li/+ x M. spretus)F1 females and from the mutant male embryos for the presence of other microsatellites known to map in the vicinity of DXMit28. The lined deletion was found to remove DXMit70, DXMit33, DXMit99, DXMit189, DXMit28 and Rps6ka3. This deletion is flanked proximally by DXMit98, Phex , DXMit180 and DXMit179, and distally by Pdha1, DXMit220, DXMit121 , 221 and DXMit21.