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MipCat
Spontaneous Allele Detail
Summary
Symbol: MipCat
Name: major intrinsic protein of lens fiber; dominant cataract
MGI ID: MGI:1856474
Synonyms: cataracta hereditaria subcapsularis
Gene: Mip  Location: Chr10:128061707-128067681 bp, + strand  Genetic Position: Chr10, 76.49 cM, cytoband D1
Alliance: MipCat page
Mutation
origin
Strain of Origin:  albino stock
Mutation
description
Allele Type:    Spontaneous
Mutation:    Transposon insertion
Inheritance:    Semidominant
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:  33 strains or lines available
Notes
This mutation was first described, under the imposing name cataracta hereditaria subcapsularis, in an albino strain of unknown origin (J:285). The probably identical "cataract Fraser" allele, MipCat-Fr, was found in the A/J strain. Most of the studies characterizing these cataract causing mutations in Mip have been carried out using MipCat-Fr, and are described under that mutation.
References
Original:  J:285 PAGET OE, [Hereditary subcapsular cataract; a new dominant allelomorph in house mouse.]. Z Indukt Abstamm Vererbungsl. 1953;85(2):238-44
All:  1 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)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory