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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Opn1sw
opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
MGI:99438
3 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Opn1swtm1.1Pugh/Opn1swtm1.1Pugh
involves: 129S6/SvEvTac * C57BL/6 * SJL 		abnormal cone electrophysiology J:185275
normal vision/eye phenotype J:185275
Opn1swtm1Pugh/Opn1swtm1Pugh
involves: 129S6/SvEvTac * C57BL/6J 		disorganized photoreceptor outer segment J:185275
normal vision/eye phenotype J:185275
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
04/16/2024
MGI 6.23 		The Jackson Laboratory