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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Efnb3tm1.1Henk
targeted mutation 1.1, Mark Henkemeyer
MGI:3026702
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Efnb3tm1.1Henk/Efnb3tm1.1Henk either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1) MGI:3026745
hm2
Efnb3tm1.1Henk/Efnb3tm1.1Henk involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3851496
cx3
Efnb3tm1.1Henk/Efnb3tm1.1Henk
Ephb2tm1Jf/Ephb2tm1Jf
Lnx1tm1Henk/Lnx1tm1Henk
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:8228084


Genotype
MGI:3026745
hm1
Allelic
Composition
Efnb3tm1.1Henk/Efnb3tm1.1Henk
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb3tm1.1Henk mutation (0 available); any Efnb3 mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice retain Eph-ephrin forward signaling and do not exhibit a hopping gait




Genotype
MGI:3851496
hm2
Allelic
Composition
Efnb3tm1.1Henk/Efnb3tm1.1Henk
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb3tm1.1Henk mutation (0 available); any Efnb3 mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mossy fiber pruning is defective
• infra-pyramidal bundle (IPB) axons are longer than in wild-type mice

cellular
• mossy fiber pruning is defective




Genotype
MGI:8228084
cx3
Allelic
Composition
Efnb3tm1.1Henk/Efnb3tm1.1Henk
Ephb2tm1Jf/Ephb2tm1Jf
Lnx1tm1Henk/Lnx1tm1Henk
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb3tm1.1Henk mutation (0 available); any Efnb3 mutation (11 available)
Ephb2tm1Jf mutation (0 available); any Ephb2 mutation (68 available)
Lnx1tm1Henk mutation (0 available); any Lnx1 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• disruption of mossy fiber axon terminal targeting





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last database update
08/05/2025
MGI 6.24
The Jackson Laboratory