Opn1mw Phenotype Annotations - Multigenic Genotypes

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Opn1mw^{tm1(OPN1LW)Nat}/Opn1mw⁺ involves: 129	abnormal vision	J:85849
Opn1mw^{tm1(OPN1LW)Nat}/Y involves: 129	abnormal vision	J:85849
Opn1mw^{tm1(OPN1LW)Nat}/Opn1mw^{tm1(OPN1LW)Nat} involves: 129	abnormal vision	J:85849
Opn1mw^{tm1(OPN1LW)Nat}/Opn1mw^{tm1(OPN1LW)Nat} Opn4^tm1Yau/Opn4^tm1Yau 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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