Opn1sw Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Opn1sw^tm1.1Pugh/Opn1sw^tm1.1Pugh involves: 129S6/SvEvTac * C57BL/6 * SJL	abnormal cone electrophysiology	J:185275
	normal vision/eye phenotype	J:185275
Opn1sw^tm1Pugh/Opn1sw^tm1Pugh 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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