Symbol Name ID |
Pten
phosphatase and tensin homolog MGI:109583 |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Muscle weakness |
Abdominal wall muscle weakness |
Skeletal muscle atrophy |
Myopathy |
Disease(s) Associated with PTEN | |||||
Bannayan-Riley-Ruvalcaba syndrome | |||||
macrocephaly-autism syndrome |
Mouse Phenotypes | increased myocardial fiber mitochondrial DNA content |
increased myocardial fiber size |
decreased cardiac muscle contractility |
abnormal muscle fiber morphology |
enhanced skeletal muscle regeneration |
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Availability | Mouse Genotype | |||||
Ptentm1.1Yxy/Ptentm1.1Yxy | ||||||
Ptentm1Hwu/Ptentm1Hwu (conditional) | ||||||
Ptentm1Hwu/Ptentm1Hwu Tg(Ckmm-cre)5Khn/? (conditional) |
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Ptentm2Mak/Ptentm2Mak Tg(Ckmm-cre)5Khn/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 04/16/2024 MGI 6.23 |
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