About   Help   FAQ
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 (28 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory