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| Nomenclature |
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Symbol:
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PhexHyp-2J
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Name:
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phosphate regulating gene with homologies to endopeptidases on the X chromosome (hypophosphatemia, vitamin D resistant rickets);
hypophosphatemia 2 Jackson
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MGI ID: |
MGI:2181653 |
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Gene:
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Phex
Location:
ChrX:157162075-157415312 bp, - strand
Genetic Position: ChrX,
72.38 cM
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Mutation
origin |
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Strain of Origin:
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C57BL/6J
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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Mutation details: A deletion of at least 7.3 kb containing exon 15 of the Phex gene was identified and confirmed by RT-PCR, genomic PCR and Southern blot analysis
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:88352
Lorenz-Depiereux B et al.,
"New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice."
Mamm Genome 2004 Mar;15(3):151-61
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All: |
1 reference(s)
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Analysis Tools
