respiratory system
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• lungs at E18.5 show arrested lung morphogenesis in late sacculation
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Analysis Tools|
Allele Symbol Allele Name Allele ID |
Sftpc+ wild type MGI:2434380 |
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| Summary |
14 genotypes
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• lungs at E18.5 show arrested lung morphogenesis in late sacculation
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• mice exhibit a median survival of 2.5 days due to lethal postnatal respiratory failure
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• lungs exhibit inflammatory infiltrate
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• mice exhibit distorted lung architecture, enlargement of airspaces, interstitial widening, and inflammatory infiltrate
• lungs at P2 exhibit heterogenous areas of thickened septae with proteinaceous fluid in the alveolar space
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• lungs exhibit interstitial widening
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• respiratory distress between P1.5 and P3.5
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• mice develop lethal postnatal respiratory failure
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• lungs exhibit inflammatory infiltrate
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| interstitial lung disease | DOID:3082 |
OMIM:PS619611 |
J:279196 | |
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• mice exhibit subtle airspace enlargement (simplified alveoli)
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• tamoxifen-treated mice develop alveolitis 2 weeks after treatment that is sustained to 4 weeks, although less severely than in homozygous mice
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• tamoxifen-treated mice develop alveolitis 2 weeks after treatment that is sustained to 4 weeks, although less severely than in homozygous mice
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| N |
• tamoxifen-treated mice do not show weight loss
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| N |
• tamoxifen-treated mice do not show early mortality
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• adult mice administered intraperitoneal tamoxifen develop moderate alveolitis and interstitial histological changes 2 weeks after induction
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• adult mice administered intraperitoneal tamoxifen develop moderate alveolitis and interstitial histological changes 2 weeks after induction
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| N |
• tamoxifen-treated mice do not show early mortality
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| N |
• tamoxifen-treated mice do not show weight loss
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• tamoxifen-treated mice show reduced density of alveoli
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• alveoli are enlarged in tamoxifen-treated mice
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• adult mice treated with tamoxifen exhibit enlargement of alveolar airspace and loss of alveolar density, indicating emphysematous changes
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
| N |
• lung morphology is not altered in tamoxifen-treated mice
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• many mice do not survive to 13 weeks after tamoxifen treatment due to high tumor burden
• mice display leaky cre expression without tamoxifen treatment and survive a few months longer than tamoxifen-treated animals
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• after tamoxifen treatment, mice show a more severe phenotype than animals with wild-type Trp53 (greater tumor size, tumor growth and tumor grade); by 3-4 weeks after tamoxifen treatment, several small adenomas of papillary nature are observed in alveoli
• at 10 weeks after tamoxifen injection, many alveoli have large tumors; tumors exhibit enlarged pleomorphic nuclei, aberrant mitosis; tumor giant cells are present
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• mice surviving to 13 weeks after tamoxifen treatment have adenocarcinomas in the alveoli of the lungs
• without tamoxifen treatment, mice develop invasive lung adenocarcinomas localized to the alveoli
• bronchioalveolar duct junctions (BADJs) appear normal ( in mice with or without tamoxifen treatment)
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• after tamoxifen treatment, mice show a more severe phenotype than animals with wild-type Trp53 (greater tumor size, tumor growth and tumor grade); by 3-4 weeks after tamoxifen treatment, several small adenomas of papillary nature are observed in alveoli
• at 10 weeks after tamoxifen injection, many alveoli have large tumors; tumors exhibit enlarged pleomorphic nuclei, aberrant mitosis; tumor giant cells are present
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• mice surviving to 13 weeks after tamoxifen treatment have adenocarcinomas in the alveoli of the lungs
• without tamoxifen treatment, mice develop invasive lung adenocarcinomas localized to the alveoli
• bronchioalveolar duct junctions (BADJs) appear normal ( in mice with or without tamoxifen treatment)
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• 8 days after tamoxifen treatment, extensive type II cell proliferation is observed compared to wild-type; however, proliferating bronchioalveolar stem cells (BASCs) are rarely observed (at 8 days, 3, 6, 10 and 13 weeks after tamoxifen treatment)
• tumor cells express type II cell markers and are highly proliferative, even without tamoxifen treatment
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• by 18 weeks after tamoxifen treatment, numerous adenomas develop in alveoli; small numbers of cells with features of malignant transformation are observed in some lung sections
• tumors are usually found in proximity to the airways, bronchioalveolar duct junctions (BADJs), or surface of the lung, but lesions are not found in the BADJs
• tumor cells are highly proliferative
• airways and BADJs retain normal architecture
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• by 18 weeks after tamoxifen treatment, numerous adenomas develop in alveoli; small numbers of cells with features of malignant transformation are observed in some lung sections
• tumors are usually found in proximity to the airways, bronchioalveolar duct junctions (BADJs), or surface of the lung, but lesions are not found in the BADJs
• tumor cells are highly proliferative
• airways and BADJs retain normal architecture
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• reduced glycolytic ATP production in AT2 cells
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• reduced glycolytic ATP production in AT2 cells
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• reduced number of AT1 cells 63 days after bleomycin-induced lung injury at age 12 months
• normal number of AT2 cells 63 days after bleomycin-induced lung injury at age 12 months
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• 63 days after bleomycin-induced lung injury at age 12 months
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• 63 days after bleomycin-induced lung injury at age 12 months
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• reduced forced vital capacity 63 days after bleomycin-induced lung injury at age 12 months
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• 63 days after bleomycin-induced lung injury at age 12 months
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• reduced lung fibrosis, better forced vital lung capacity, better lung compliance and increased number of alveolar type I (AT1) cells 63 days after bleomycin-induced lung injury at age 12 months
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• reduced lung fibrosis, better forced vital lung capacity, better lung compliance and increased number of alveolar type I (AT1) cells 63 days after bleomycin-induced lung injury at age 12 months
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• reduced lung fibrosis, better forced vital lung capacity, better lung compliance and increased number of alveolar type I (AT1) cells 63 days after bleomycin-induced lung injury at age 12 months
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• reduced lung fibrosis, better forced vital lung capacity, better lung compliance and increased number of alveolar type I (AT1) cells 63 days after bleomycin-induced lung injury at age 12 months
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• mice die 14 weeks or less after tamoxifen administration
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• at 6-8 weeks of age, animals administered 1dose or 4 doses of tamoxifen develop widespread adenomas in the alveoli by 14 weeks of age, but the bronchoalveolar duct junction remains tumor-free
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• at 6-8 weeks of age, animals administered 1dose or 4 doses of tamoxifen develop widespread adenocarcinomas in the alveoli by 14 weeks of age
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• at 6-8 weeks of age, animals administered 1dose or 4 doses of tamoxifen develop widespread adenomas in the alveoli by 14 weeks of age, but the bronchoalveolar duct junction remains tumor-free
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• at 2 weeks after tamoxifen treatement, brochioalveolar duct junctions (BADJ) appear normal, but small adenomas occur in the alveoli; these progress to adenocarcinoma but the BADJ remain histologically normal
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
| N |
• bleomycin, tamoxifen-treated mice develop fibrosis and lung collagen content as in control mice
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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 10/06/2026 MGI 6.29 |
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