Symbol Name ID |
Fbxw7
F-box and WD-40 domain protein 7 MGI:1354695 |
Darker colors indicate more annotations |
Human Phenotypes | Recurrent pneumonia |
Laryngeal cleft |
Disease(s) Associated with FBXW7 | ||
developmental delay, hypotonia, and impaired language |
Mouse Phenotypes | impaired lung alveolus development |
abnormal pulmonary alveolus wall morphology |
thick pulmonary interalveolar septum |
abnormal respiratory system physiology |
respiratory failure |
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Availability | Mouse Genotype | |||||
Fbxw7tm1.1Iken/Fbxw7+ | ||||||
Fbxw7tm1Itom/Fbxw7+ Tg(Pgk1-cre)1Lni/0 (conditional) |
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 04/30/2024 MGI 6.23 |
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