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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nfibtm1Hsch
targeted mutation 1, Heinrich Schrewe
MGI:2178748
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nfibtm1Hsch/Nfibtm1Hsch involves: 129S1/Sv * C57BL/6 MGI:2178810
ht2
Nfibtm1Hsch/Nfib+ involves: 129S1/Sv * C57BL/6 MGI:3653744


Genotype
MGI:2178810
hm1
Allelic
Composition
Nfibtm1Hsch/Nfibtm1Hsch
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfibtm1Hsch mutation (0 available); any Nfib mutation (91 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes are born alive but die within 15 min after birth due to respiratory failure

respiratory system
• at E18.5 and shortly after birth, mutant lungs appear developmentally immature with a gland-like appearance
• mutant lungs fail to develop beyond the late pseudoglandular or early canalicular stage
• at E16.5, branching morphogenesis is slightly inhibited
• at E18.5, lobar branching from the primary bronchi is observed but further branching generates an undifferentiated primordial respiratory system
• at E18.5, the terminal buds are embedded within extensive mesenchyme and terminal sacs are absent
• at E18.5, terminal sacs are absent
• at E18.5, mutant lungs exhibit undifferentiated type I and II pneumocytes
• despite normal size and lobation, homozygous mutant lungs have a 40% higher wet weight than wild-type lungs; however, no difference in lung dry weight is observed
• newborn homozygotes display severe lung hypoplasia
• mutant lungs fail to float on water, indicating that they were never inflated with air
• at autopsy, all E18.5 mutant embryos and neonates contain air in their stomach and intestine, suggesting improper breathing
• newborn homozygotes exhibit respiratory distress; however, no abnormalities are noted in the ribs, larynx, trachea, or other skeletal elements
• newborn homozygotes make visible efforts to breathe but die of respiratory failure

vision/eye
• all homozygous mutant E18.5 embryos and neonates have open eyes due to failure of eyelid fusion

homeostasis/metabolism
• newborn homozygotes become cyanotic shortly after birth




Genotype
MGI:3653744
ht2
Allelic
Composition
Nfibtm1Hsch/Nfib+
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfibtm1Hsch mutation (0 available); any Nfib mutation (91 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• heterozygous mutant lungs are arrested at the late canalicular stage with only focal transition of tissue to the terminal sac stage
• the already developed terminal sacs protect heterozygotes from death due to asphyxia; as a result, all heterozygotes survive and appear overtly normal
• continued postnatal maturation of lungs proceeds and lung histology is indistinguishable from that of wild-type mice at 8 weeks postpartum
• at E18.5, only a few terminal sacs surrounded by thick mesenchyme are observed
• at E18.6, heterozygous mutant lungs display a larger mesenchymal compartment and thicker interalveolar septae
• heterozygous mutant lungs have a 16% higher wet weight than wild-type lungs, despite normal size and lobation; however, no difference in lung dry weight is observed
• at E18.5 and shortly after birth, heterozygous mutant lungs are slightly hypoplastic and premature relative to wild-type lungs





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory