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Phenotypes Associated with This Genotype
Genotype
MGI:4839089
Allelic
Composition
Fbn1tm1.2Lysa/Fbn1+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbn1tm1.2Lysa mutation (0 available); any Fbn1 mutation (171 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Fragmentation of aortic root elastic lamellae in Fbn1tm1.2Lysa/Fbn1+ mice

cardiovascular system
• at 2 months, mice exhibit progressive fragmentation of the aortic elastic lamellae with age unlike wild-type mice

muscle
• at P8, mice exhibit fragmentation of the microfibril network unlike in wild-type mice
• however, early postnatal assembly of microfibril networks is normal
• at P8, mice exhibit fragmentation of the microfibril network unlike in wild-type mice
• however, early postnatal assembly of microfibril networks is normal

skeleton
• at P8, mice exhibit fragmentation of the microfibril network unlike in wild-type mice
• however, early postnatal assembly of microfibril networks is normal

integument
• at P8, mice exhibit fragmentation of the microfibril network unlike in wild-type mice
• however, early postnatal assembly of microfibril networks is normal


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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory