Symbol Name ID |
Braf
Braf transforming gene MGI:88190 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertonia |
Hypotonia |
Generalized hypotonia |
Neonatal hypotonia |
Disease(s) Associated with BRAF | ||||
cardiofaciocutaneous syndrome | ||||
cardiofaciocutaneous syndrome 1 | ||||
Noonan syndrome 7 | ||||
Noonan syndrome with multiple lentigines 3 |
Mouse Phenotypes | abnormal myocardial fiber morphology |
increased myocardial fiber size |
abnormal myocardial trabeculae morphology |
thin myocardium compact layer |
increased cardiac muscle contractility |
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Availability | Mouse Genotype | |||||
Braftm1Bbd/Braf+ | ||||||
Braftm1Tumg/Braf+ Tg(CAG-cre)2Osb/0 (conditional) |
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Braftm2Cpri/Braf+ Tg(CMV-cre)1Cgn/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 03/12/2024 MGI 6.23 |
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