All Phenotypes Opn5<tm1.1Lan> MGI Mouse

Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Opn5^tm1.1Lan
targeted mutation 1.1, Richard A Lang
MGI:5897189

Summary

2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
cx1	Opn5^tm1.1Lan/Opn5^tm1.1Lan Per2^tm1Jt/Per2⁺	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6N * FVB/N	MGI:5897196
cx2	Opn5^tm1.1Lan/Opn5^tm1.1Yau Per2^tm1Jt/Per2⁺	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6N * FVB/N	MGI:5897197

Allelic Composition	Opn5^tm1.1Lan/Opn5^tm1.1Lan Per2^tm1Jt/Per2⁺
Genetic Background	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6N * FVB/N

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Opn5^tm1.1Lan mutation (0 available); any Opn5 mutation (19 available)
Per2^tm1Jt mutation (2 available); any Per2 mutation (71 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

vision/eye

abnormal eye physiology ( J:227078 )

• ex vivo corneal photoentrainment is abolished

Allelic Composition	Opn5^tm1.1Lan/Opn5^tm1.1Yau Per2^tm1Jt/Per2⁺
Genetic Background	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6N * FVB/N

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Opn5^tm1.1Lan mutation (0 available); any Opn5 mutation (19 available)
Opn5^tm1.1Yau mutation (0 available); any Opn5 mutation (19 available)
Per2^tm1Jt mutation (2 available); any Per2 mutation (71 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

vision/eye

abnormal eye physiology ( J:227078 )

• ex vivo corneal photoentrainment is abolished

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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