Ppp1r13l^woe2
Spontaneous Allele Detail

Summary

• Symbol: Ppp1r13l^woe2
• Name: protein phosphatase 1, regulatory subunit 13 like; waved with open eyelids 2
• MGI ID: MGI:5449625
• Synonyms: Ppp1r13l^{deltaexon9-11}
• Gene: Ppp1r13l Location: Chr7:19093674-19112458 bp, + strand Genetic Position: Chr7, 9.62 cM
• Alliance: Ppp1r13l^woe2 page

Ppp1r13l^woe2/Ppp1r13l^woe2 mice exhibit open eyelids at birth and eye abnormalities

Show the 4 phenotype image(s) involving this allele.

Mutation origin

• Strain of Origin: C57BL/6 x 129X1/SvJ

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: This allele contains a spontaneous 1308 bp deletion between intron 8 and intron 11. The resulting protein is truncated at amino acid 608 of 824. (J:190557)
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

11 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Ppp1r13l Mutation: 39 strains or lines available

References

• Original: J:190557 Toonen J, et al., Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene. BMC Genet. 2012;13:76
• All: 1 reference(s)