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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bmpertm1Cpat
targeted mutation 1, Cam Patterson
MGI:3840517
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bmpertm1Cpat/Bmpertm1Cpat involves: 129P2/OlaHsd * C57BL/6 MGI:3840521
ht2
Bmpertm1Cpat/Bmper+ involves: 129P2/OlaHsd * C57BL/6 MGI:3840522


Genotype
MGI:3840521
hm1
Allelic
Composition
Bmpertm1Cpat/Bmpertm1Cpat
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bmpertm1Cpat mutation (0 available); any Bmper mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Bmpertm1Cpat/Bmpertm1Cpat mice die at birth and have widespread tissue-specific defects

mortality/aging

embryo
• mice exhibit widespread tissue-specific defects during embryonic development




Genotype
MGI:3840522
ht2
Allelic
Composition
Bmpertm1Cpat/Bmper+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bmpertm1Cpat mutation (0 available); any Bmper mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Delayed branching morphogenesis and inadequately expanded alveoli in Bmpertm1Cpat/Bmper+ lungs

respiratory system
• overgrowth of mesenchymal cells appears to prevent complete alveoli expansion with smaller and fewer terminal sacs that are separated by thickened interstitial mesenchyme unlike in wild-type mice
• at E18.5, lungs have fewer apoptotic cells than in wild-type lungs
• branching morphogenesis in the lung is delayed compared to in wild-type mice
• however, lung differentiation and cell proliferation are normal
• smaller and fewer terminal sacs separated by thickened interstitial mesenchyme
• at E18.5, the ratio of type II epithelial cells to total distal cells is increased compared to in wild-type mice

embryo
• mice exhibit widespread tissue-specific defects during embryonic development

cardiovascular system
• in a model of oxygen-induced retinopathy (5 days of hyperoxia followed by hypoxia), mutants show an increased rate of retinal revascularization and faster recovery of the retinal vascular bed
• hypoxic retinas show a more dense and complex network of newly formed vessels, with increased numbers of branching points and angiogenic sprouts at the leading edge of the newly formed vasculature

vision/eye
• in a model of oxygen-induced retinopathy (5 days of hyperoxia followed by hypoxia), mutants show an increased rate of retinal revascularization and faster recovery of the retinal vascular bed
• hypoxic retinas show a more dense and complex network of newly formed vessels, with increased numbers of branching points and angiogenic sprouts at the leading edge of the newly formed vasculature





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
11/12/2024
MGI 6.24
The Jackson Laboratory