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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    17
  • Reference
    J:89010 Paffenholz R, et al., Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase. Genes Dev. 2004 Mar 1;18(5):486-91
  • ID
    MGI:3579558
Genes
GeneAlleleAssay TypeDescription
Nox3
Tiam2
D17Ingm4
D17Ingm9
D17Brg18
D17Brg198
Notes
  • Experiment
    The head-tilt R96 (hetR96) mutation was mapped to an interval on proximal mouse Chromosome 17 between D17Ing9 and the centromere using 375 (C3HeB/FeJ-Nox3het-R96 x C57BL/6J)F2 intercross animals. BAC clone RP23-27N1 was found to carry the gene as evidenced by BAC transgenic rescue experiments. This clone carries the following candidate genes in descending order from the centromere: Racgef1 - Tiam2 - Cldn20 - Nox3. Sequence analysis revealed a premature stop mutation in the Nox3 gene in hetR96 animals.

    (Racgef1 and Cldn20 do not exist in MGI as of 6/14/05)

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
04/16/2024
MGI 6.23
The Jackson Laboratory