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Mipnat
Spontaneous Allele Detail
Summary
Symbol: Mipnat
Name: major intrinsic protein of lens fiber; nat
MGI ID: MGI:5688484
Gene: Mip  Location: Chr10:128061707-128067681 bp, + strand  Genetic Position: Chr10, 76.49 cM, cytoband D1
Alliance: Mipnat page
Mutation
origin
Strain of Origin:  SJL/J
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsSpontaneous mutation resulted in a G to A point mutation that codes for the amino acid substitution of arginine for glycine at position 211 (G211R). (J:273897)
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:273897 Takahashi G, et al., A novel missense mutation of Mip causes semi-dominant cataracts in the Nat mouse. Exp Anim. 2017 Aug 5;66(3):271-282
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
01/28/2026
MGI 6.24
The Jackson Laboratory