About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3641316
Allelic
Composition
Tbx1tm1(Fgf8)Vite/Tbx1tm1(Fgf8)Vite
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx1tm1(Fgf8)Vite mutation (1 available); any Tbx1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• hypoplasia of the caudal pharyngeal apparatus is observed at E 10.5

craniofacial
• hypoplasia of the caudal pharyngeal apparatus is observed at E 10.5

cardiovascular system
• one incidence of double aortic arch with aortic dilation was observed
• PTA associated with the right or left aortic arch is observed at E18.5; in all affected mutants, PTA communicates solely with the right ventricle
• a ventricular septal defect is observed
• there is a loss of continuity between the mitral and semilunar valves


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
04/16/2024
MGI 6.23
The Jackson Laboratory