Mip⁺
Allele Detail

Summary

• Symbol: Mip⁺
• Name: major intrinsic protein of lens fiber; wild type
• MGI ID: MGI:2153197
• Gene: Mip Location: Chr10:128061707-128067681 bp, + strand Genetic Position: Chr10, 76.49 cM, cytoband D1

Mutation origin

• Strain of Origin: Not Applicable

Mutation description

• Allele Type: Not Specified
• Inheritance: Not Specified

Disease models

Expression

In Mice Carrying this Mutation:	11 assay results
In Structures Affected by this Mutation:	3 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 Mip Mutation: 31 strains or lines available

References

• Original: J:70225 Sidjanin DJ, et al., A 76-bp deletion in the mip gene causes autosomal dominant cataract in hfi mice. Genomics. 2001 Jun 15;74(3):313-9
• All: 4 reference(s)