About   Help   FAQ
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
Loading...
View phenotypes for all genotypes (concatenated display).
Disease models
Loading...
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:  100 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
07/23/2014
MGI 5.18
The Jackson Laboratory