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Mapping Data
Experiment
  • Experiment
    CROSS
  • 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:1341566
Genes
GeneAlleleAssay TypeDescription
D13Mit206
Foxc1 Foxc1ch visible phenotype
D13Mit294
D13Mit307
CROSS
  • Type
    Intercross
  • Female Parent
    <n> <n> <n> <n>/<b> <b> <b> <b>
  • Strain
    (CHMU/Le-+ Foxc1 MOLF/Ei or CHMU/Le-+ Foxc1 CAST/Ei)F1
  • Male Parent
    <n> <n> <n> <n>/<b> <b> <b> <b>
  • Strain
    (CHMU/Le-+ Foxc1 MOLF/Ei or CHMU/Le-+ Foxc1 CAST/Ei)F1
  • Allele 1
    n from CHMU/LeJ
  • Allele 2
    b from CAST/Ei or MOLF/Ei
2x2 Data Reported
Marker 1 Marker 2 # Recombinants # Parentals
D13Mit206 Foxc1 18 606
Foxc1 D13Mit294 0 556
Foxc1 D13Mit307 1 604
D13Mit294 D13Mit307 1 604

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
11/12/2024
MGI 6.24
The Jackson Laboratory