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| Nomenclature |
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Symbol:
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PhexHyp
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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
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MGI ID: |
MGI:1857312 |
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Synonyms: |
Hyp |
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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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PhexHyp/Y male or PhexHyp/Phex+ female (front) with wild type mouse (rear)
Show the 6 image(s) involving this allele.
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Mutation
origin |
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Strain of Origin:
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Not Specified
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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The mutation in the Hyp mouse is a deletion that includes exons 16-22 of the gene. (J:34935, J:38621, J:39093, J:47232, J:54052)
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Inheritance: | |
Semidominant |
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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:13533
Eicher EM et al.,
"Hypophosphatemia (Hyp); Chr 7 linkage."
Mouse News Lett 1972;47():36
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All: |
100 reference(s)
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Analysis Tools
