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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
GeneAlleleAssay TypeDescription
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory