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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Epha4tm1.1Bzh
targeted mutation 1.1, Binhai Zheng
MGI:4430285
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Epha4tm1.1Bzh/Epha4tm1.1Bzh involves: 129S7/SvEvBrd * C57BL/6 * SJL MGI:4430289
cn2
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129S7/SvEvBrd MGI:5614429
cn3
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Tg(Slc17a6-icre)1Oki/0
involves: 129S7/SvEvBrd * C57BL/6 MGI:5614433
cn4
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Tg(Hoxb8-cre)1403Uze/0
involves: 129S7/SvEvBrd * C57BL/6 * DBA/2 MGI:5614430
cn5
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Isl1tm1(cre)Sev/Isl1+
Tg(Hlxb9-GFP)1Tmj/0
involves: 129S/Sv * Black Swiss * C57BL/6J * CD-1 * FVB/N MGI:6406420
cn6
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Tg(Hlxb9-GFP)1Tmj/0
Twist2tm1(cre)Dor/Twist2+
involves: 129S/Sv * C57BL/6J * CD-1 * FVB/N MGI:6406424


Genotype
MGI:4430289
hm1
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:5614429
cn2
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Emx1tm1(cre)Krj/Emx1+
Genetic
Background
involves: 129S2/SvPas * 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Krj mutation (2 available); any Emx1 mutation (34 available)
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
Epha4tm1.2Bzh mutation (0 available); any Epha4 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• unlike in germ line null mice, the gait is similar to that in wild-type mice

nervous system
• increased midline re-crossing of axons dorsal to the central canal in both the cervical enlargement and lumbar spinal cord




Genotype
MGI:5614433
cn3
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Tg(Slc17a6-icre)1Oki/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
Epha4tm1.2Bzh mutation (0 available); any Epha4 mutation (66 available)
Tg(Slc17a6-icre)1Oki mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• quadrupedal hopping gait is dominant at all locomotor frequencies
• occasional alternating gait is seen at lower frequencies

nervous system
• increase in axon midline crossing
• significantly wider gap between the central canal and the ventral edge of the dorsal funiculus
• wider and the distance from the ventral edge to the surface of the spinal cord is shorter; however, the total area is not different from controls
• chemically and electrically stimulated locomotor-like activity in isolated spinal cord preparations induces a synchronous "hopping" locomotor-like activity rather than an alternating locomotor-like activity




Genotype
MGI:5614430
cn4
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.2Bzh
Tg(Hoxb8-cre)1403Uze/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
Epha4tm1.2Bzh mutation (0 available); any Epha4 mutation (66 available)
Tg(Hoxb8-cre)1403Uze mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• dominant hopping hindlimb gait at all frequencies of locomotion with occasional alternating gait at frequencies around and less than 4 Hz

nervous system
• significantly wider gap between the central canal and the ventral edge of the dorsal funiculus
• wider and the distance from the ventral edge to the surface of the spinal cord is shorter; however, the total area is not different from controls




Genotype
MGI:6406420
cn5
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Isl1tm1(cre)Sev/Isl1+
Tg(Hlxb9-GFP)1Tmj/0
Genetic
Background
involves: 129S/Sv * Black Swiss * C57BL/6J * CD-1 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
Isl1tm1(cre)Sev mutation (1 available); any Isl1 mutation (33 available)
Tg(Hlxb9-GFP)1Tmj mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• embryos show an increase in the number of abducens nerve bundles following exit from the hindbrain, reductions in both abducens nerve length and diameter at the orbit and larger wandering abducens nerve bundles that exhibit enhanced nerve pausing at the midpoint decision within the abducens fasciculation region
• however, trochlear nerve and first cervical spine projections are normal
• abducens nerve length is reduced and nerve diameter is thinner near the orbit in embryos




Genotype
MGI:6406424
cn6
Allelic
Composition
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Tg(Hlxb9-GFP)1Tmj/0
Twist2tm1(cre)Dor/Twist2+
Genetic
Background
involves: 129S/Sv * C57BL/6J * CD-1 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm1.1Bzh mutation (1 available); any Epha4 mutation (66 available)
Tg(Hlxb9-GFP)1Tmj mutation (3 available)
Twist2tm1(cre)Dor mutation (0 available); any Twist2 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the abducens nerve exits the hindbrain with fewer nerve bundles, which initially wander in the mesenchymal area adjacent to the hindbrain exit before completely stalling in the mesenchyme leading to a reduction in abducens length and complete lack of both abducens innervation near the orbit and aberrant tracking with the facial nerve
• however, trochlear nerve and first cervical spine projections are normal





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory