Phex^Hyp
Spontaneous Allele Detail

Summary

• Symbol: Phex^Hyp
• Name: phosphate regulating endopeptidase homolog, X-linked; hypophosphatemia
• MGI ID: MGI:1857312
• Synonyms: Hyp, Op
• Gene: Phex Location: ChrX:155945071-156198282 bp, - strand Genetic Position: ChrX, 72.38 cM
• Alliance: Phex^Hyp page

Phex^Hyp/Y male or Phex^Hyp/Phex⁺ female (front) with wild type mouse (rear)

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

Mutation origin

• Strain of Origin: B6.Cg-Qki^qk-v

Mutation description

• Allele Type: Spontaneous (Not Specified)
• 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, J:85297)
• Inheritance: Semidominant

Disease models

Expression

In Mice Carrying this Mutation:	5 assay results 4 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	19 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Phex Mutation: 21 strains or lines available

References

• Original: J:30724 Dickie MM, New Mutants: chs-1, Op, lm, sh-1^r, A^sy, td. Mouse News Lett. 1969;41:30-1
• All: 150 reference(s)