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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Efnb2tm3.1Kln
targeted mutation 3.1, Rudiger Klein
MGI:2182632
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Efnb2tm3.1Kln/Efnb2tm3.1Kln involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3795270


Genotype
MGI:3795270
hm1
Allelic
Composition
Efnb2tm3.1Kln/Efnb2tm3.1Kln
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Efnb2tm3.1Kln mutation (0 available); any Efnb2 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
N
• principal pattern of crainial neural crest cell migration is maintained
• about 8% of embryos have branchial arches that are reduced in size
• general growth retardation observed at E9.5
• defects are observed in yolk sac vasculature

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
• at E9.5, anterior cardinal veins have not formed; endothelial cells are arranged loosely and irregularly and do not form a tubular structure
• inflation of pericard is observed at E9.5

craniofacial
• about 8% of embryos have branchial arches that are reduced in size





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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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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory