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Phenotypes Associated with This Genotype
Genotype
MGI:5462243
Allelic
Composition		 Optctm1.1Pnb/Optctm1.1Pnb
Genetic
Background		 involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Optctm1.1Pnb mutation (0 available); any Optc mutation (43 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
cardiovascular system
abnormal induced retina neovascularization ( J:191528 )
• in an oxygen-induced retinopathy model, mice exhibit more preretinal neovascularization compared with wild-type mice

vision/eye
abnormal induced retina neovascularization ( J:191528 )
• in an oxygen-induced retinopathy model, mice exhibit more preretinal neovascularization compared with wild-type mice

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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Send questions and comments to User Support. 		last database update
06/12/2024
MGI 6.13 		The Jackson Laboratory