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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Flnatm1.1Caw
targeted mutation 1.1, Christopher A Walsh
MGI:3699305
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Flnatm1.1Caw/Y
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S4/SvJae * C57BL/6 * CBA MGI:3699953


Genotype
MGI:3699953
cn1
Allelic
Composition
Flnatm1.1Caw/Y
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Flnatm1.1Caw mutation (1 available); any Flna mutation (18 available)
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• males survive until birth but die on first postnatal day

cardiovascular system
• blood vessels in brain are dilated
• males show abnormal outflow tracts including interrupted aortic arch, but less severe than Flnatm1.1Caw mutant males
• some adherens junctions (AJs) are unidentifiable, with excessive membrane ruffles at sites where AJs normally form
• endothelial cells are poorly organized with clusters or multiple layers and gaps in outflow tract
• males show abnormal outflow tracts including PTA, but less severe than Flnatm1.1Caw mutant males
• endothelial cells are poorly organized with clusters or multiple layers and gaps in endocardial cushion

homeostasis/metabolism
• males are cyanotic at birth, indicating hypoxemia

nervous system
• at E14.5, surviving mutants have smaller but grossly normal brains, with thinner cortical plate

behavior/neurological
N
• no heterotopic neurons or migratory arrest are seen in mutant brains





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory