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Phenotypes Associated with This Genotype
Genotype
MGI:5426907
Allelic
Composition
Rgs11tm1Lex/Rgs11tm1Lex
Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rgs11tm1Lex mutation (2 available); any Rgs11 mutation (31 available)
Rgs7tm1Cjch mutation (0 available); any Rgs7 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Rgs7tm1Cjch/Rgs7tm1Cjch Rgs11tm1Lex/Rgs11tm1Lex mice have no ERG b-waves and contain ultrastructural defects in the retinal outer plexiform layer

mortality/aging
N
• normal viability

reproductive system
N
• normal fertility

vision/eye
• fewer triads per spherule compared to in wild-type mice
• fewer spherules with ribbons compared to in wild-type mice
• absent b-wave under scotopic and photopic conditions
• absent b-wave under scotopic and photopic conditions


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
03/18/2025
MGI 6.24
The Jackson Laboratory