About   Help   FAQ
MipCat-Lop
Spontaneous Allele Detail
Summary
Symbol: MipCat-Lop
Name: major intrinsic protein of lens fiber; cataract lens opacity
MGI ID: MGI:1857105
Gene: Mip  Location: Chr10:128061707-128067681 bp, + strand  Genetic Position: Chr10, 76.49 cM, cytoband D1
Alliance: MipCat-Lop page
Mutation
origin
Strain of Origin:  STOCK Rb(6.15)1Ald
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA G-to-C transversion at position 151 of the encoded mRNA results in a non-conservative change at amino acid 51 from alanine to proline (p.A51P). This mutation inhibits targeting of the mutant product to the cell membrane. (J:31574)
Inheritance:    Semidominant
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
Expression
In Mice Carrying this Mutation: 5 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: 1 strain available      Cell Lines: 0 lines available
Carrying any Mip Mutation:  33 strains or lines available
References
Original:  J:6702 Lyon MF, et al., Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse. Genet Res. 1981 Dec;38(3):337-41
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory