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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Efnb2tm1Kln
targeted mutation 1, Rudiger Klein
MGI:2182626
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Efnb2tm1Kln/Efnb2tm1Kln involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3795265


Genotype
MGI:3795265
hm1
Allelic
Composition
Efnb2tm1Kln/Efnb2tm1Kln
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb2tm1Kln mutation (0 available); any Efnb2 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
N
• early branchial arch and neural crest formation and migration appears to occur normally in mutants at E8.5
• principal pattern of crainial neural crest cell migration is maintained
• agenesis of aortic arches is found in >90% of embryos at E9.5, even if only mild hypoplasia of the hyoid arch is present
• at E9.5, late migration of neural crest cells into branchial arches is severely disrupted
• few crabp1-positive cells are detected in second aortic arch, but are found scattered and invading adjacent areas that are devoid of these cells in controls
• in hindbrain, stream of migrating cells is much wider than in controls without the clear separation from adjacent tissue seen in controls
• defect is specific and does not cause general disruption of patterning and migration in hindbrain region
• some embryos display mild hypoplasia of hyoid arches
• defect is most pronounced in central part and less prominent in distal and proximal regions
• second branchial arch is absent in some embryos (34%) at E9.5
• second branchial arch is reduced in size in some embryos (55%) at E9.5
• general growth retardation observed at E9.5

growth/size/body
• general growth retardation observed at E9.5

cardiovascular system
• intersomitic vessels form defectively, with numerous aberrant branches and sprouts invading somitic tissue instead of respecting somitic boundaries as seen in wild-type embryos at E9.5
• arrest of angiogenesis in the head at primitive capillary plexus stage is observed at E9.5
• agenesis of aortic arches is found in >90% of embryos at E9.5, even if only mild hypoplasia of the hyoid arch is present
• defects in formation of cardinal veins are seen in E9.5 embryos

craniofacial
• agenesis of aortic arches is found in >90% of embryos at E9.5, even if only mild hypoplasia of the hyoid arch is present
• some embryos display mild hypoplasia of hyoid arches
• defect is most pronounced in central part and less prominent in distal and proximal regions
• second branchial arch is absent in some embryos (34%) at E9.5
• second branchial arch is reduced in size in some embryos (55%) at E9.5

cellular
• at E9.5, late migration of neural crest cells into branchial arches is severely disrupted
• few crabp1-positive cells are detected in second aortic arch, but are found scattered and invading adjacent areas that are devoid of these cells in controls
• in hindbrain, stream of migrating cells is much wider than in controls without the clear separation from adjacent tissue seen in controls
• defect is specific and does not cause general disruption of patterning and migration in hindbrain region





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory