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Symbol Name ID |
Fryl
FRY like transcription coactivator MGI:1919563 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intraventricular hemorrhage |
Dextrocardia |
Atrial septal defect |
Patent foramen ovale |
Ventricular septal defect |
Atrioventricular canal defect |
Partial atrioventricular canal defect |
Tetralogy of Fallot |
Interrupted aortic arch |
Peripheral pulmonary artery stenosis |
Patent ductus arteriosus |
Aortic valve stenosis |
Pulmonic stenosis |
Pulmonary arterial hypertension |
Asplenia |
Polysplenia |
| Disease(s) Associated with FRYL | ||||||||||||||||
| Pan-Chung-Bellen syndrome |
| Mouse Phenotypes | abnormal placental labyrinth vasculature morphology |
placenta hemorrhage |
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| Availability | Mouse Genotype | ||
| Fryltm1b(KOMP)Wtsi/Fryltm1b(KOMP)Wtsi | |||
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 05/19/2026 MGI 6.24 |
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