About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5449367
Allelic
Composition
MitfMi/Mitf+
Vsx2tm1.1Eml/Vsx2tm1.1Eml
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MitfMi mutation (3 available); any Mitf mutation (72 available)
Vsx2tm1.1Eml mutation (0 available); any Vsx2 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

The dominant negative MitfMi allele restores retinal development in the Vsx2 mutants

vision/eye
• substantial improvements in eye size, tissue histology and retinal neurogenesis compared to mice homozygous for Vsx2tm2.1Eml alone
• substantial improvements in eye size compared to mice homozygous for Vsx2tm1.1Eml alone


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
05/07/2024
MGI 6.23
The Jackson Laboratory