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PhexHyp
Spontaneous Allele Detail
Nomenclature
Symbol: PhexHyp
Name: phosphate regulating endopeptidase homolog, X-linked; hypophosphatemia
MGI ID: MGI:1857312
Synonyms: Hyp
Gene: Phex  Location: ChrX:157162075-157415312 bp, - strand  Genetic Position: ChrX, 72.38 cM
PhexHyp/Y male or PhexHyp/Phex+ female (front) with wild type mouse (rear)

Show the 6 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
    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)
Inheritance:    Semidominant
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 5 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Phex Mutation:  11 strains or lines available
References
Original:  J:13533 Eicher EM, et al., Hypophosphatemia (Hyp); Chr 7 linkage. Mouse News Lett. 1972;47:36
All:  104 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/23/2015
MGI 5.22
The Jackson Laboratory