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Symbol Name ID |
Eogt
EGF domain specific O-linked N-acetylglucosamine transferase MGI:2141669 |
| Darker colors indicate more annotations |
| Human Phenotypes | Gastrointestinal hemorrhage |
Portal vein thrombosis |
Right atrial enlargement |
Atrial septal defect |
Patent foramen ovale |
Ventricular septal defect |
Right ventricular hypertrophy |
Tetralogy of Fallot |
Bicuspid aortic valve |
Abnormal pulmonary valve morphology |
Hypoplastic left heart |
Pulmonary artery atresia |
Pulmonary artery stenosis |
Patent ductus arteriosus |
Arteriovenous malformation |
Aortic valve stenosis |
Pulmonic stenosis |
Hypertension |
Portal hypertension |
Pulmonary arterial hypertension |
Splenomegaly |
Hypersplenism |
Cavernous hemangioma |
Cutis marmorata |
| Disease(s) Associated with EOGT | ||||||||||||||||||||||||
| Adams-Oliver syndrome |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal angiogenesis |
increased vascular permeability |
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| Availability | Mouse Genotype | |||
| Eogttm1.2Okaj/Eogttm1.2Okaj | ||||
| Eogttm1.1Okaj/Eogttm1.1Okaj Tg(Tek-cre)1Ywa/0 (conditional) |
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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 07/05/2024 MGI 6.24 |
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