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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Opn1mw
opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)
MGI:1097692
2 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Opn1mwtm1(OPN1LW)Nat/Opn1mw+
involves: 129 		abnormal vision J:85849
Opn1mwtm1(OPN1LW)Nat/Y
involves: 129 		abnormal vision J:85849
Opn1mwtm1(OPN1LW)Nat/Opn1mwtm1(OPN1LW)Nat
involves: 129 		abnormal vision J:85849
Opn1mwtm1(OPN1LW)Nat/Opn1mwtm1(OPN1LW)Nat
Opn4tm1Yau/Opn4tm1Yau
involves: 129 		abnormal visual contrast sensitivity J:199509
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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04/16/2024
MGI 6.23 		The Jackson Laboratory