Mapping Data

Experiment

• Experiment
  TEXT-Radiation Hybrid
• Chromosome
  13
• Reference
  J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
• ID
  MGI:1341569

Genes

Gene	Assay Type	Description
D13Mit81
D13Mit206
Foxq1	PCR amplified length variant	Hfh1-pA, Hfh1-pB , Hfh1-pC, Hfh1-pD
Foxc1
D13Mit294
D13Mit307
D13Mit265
D13Mit116

Notes

• Experiment
  Hfh1 was localized in relation to other SSLP markers on mouse Chromosome 13 by radiation hybrid mapping using the T31 RH panel. The order of markers was: centromere - D13Mit81 - D13Mit206 - Hfh1 - Mf1 - D13Mit294 - D13Mit307 - D13Mit265 - D13Mit116. Thisis consistent with the results obtained from the genetic and physical map. Analysis of the radiation hybrid data suggested that the Hfh1 gene was ~470kb proximal to Mf1.