Ppp1r13l^wa3-J
Spontaneous Allele Detail

Summary

• Symbol: Ppp1r13l^wa3-J
• Name: protein phosphatase 1, regulatory subunit 13 like; waved 3 Jackson
• MGI ID: MGI:3813487
• Gene: Ppp1r13l Location: Chr7:19093674-19112458 bp, + strand Genetic Position: Chr7, 9.62 cM
• Alliance: Ppp1r13l^wa3-J page

Sparse hair phenotype of the Ppp1r13l^wa3-J/Ppp1r13l^wa3-J mouse

Show the 2 phenotype image(s) involving this allele.

Mutation origin

• Strain of Origin: BALB/cJ

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• The underlying mutation is a 4 base pair deletion in exon 12.
• Inheritance: Recessive

Disease models

Expression

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	4 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Ppp1r13l Mutation: 39 strains or lines available

Notes

Phenotypic Similarity to Human Syndrome: novel autosomal recessive cardio-cutaneous syndrome (J:264272).

References

• Original: J:146206 Karst SY, et al., Waved 3 Jackson; a new remutation in the Ppp1r13l gene. MGI Direct Data Submission. 2009
• All: 2 reference(s)