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Mapping Data
Experiment
  • Experiment
    TEXT
  • Chromosome
    X
  • Reference
    J:38621 Strom TM, et al., Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia. Hum Mol Genet. 1997 Feb;6(2):165-71
  • ID
    MGI:48342
Genes
GeneAlleleAssay TypeDescription
Phex PhexHyp Southern analysis Phex cDNA15, Phex cDNA13
Notes
  • Experiment
    Southern analysis using probes specific for the 3' portion of Phex against C57BL/6J, C57BL/6J-Hyp/Y and (C57BL/6J-Hyp/Y)F1 genomic DNA showed that the 3' portion of Phex, corresponding to human exons 16-22, is deleted in Hyp mice. This data maps the Hyp deletion breakpoint within Phex exons 15 and 16 on mouse Chromosome X, making Hyp allelic to Phex.

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
11/19/2024
MGI 6.24
The Jackson Laboratory