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Symbol Name ID |
Acvrl1
activin A receptor, type II-like 1 MGI:1338946 |
| Darker colors indicate more annotations |
| Human Phenotypes | Pulmonary hemorrhage |
Pulmonary arteriovenous malformation |
Pulmonary arterial hypertension |
Pulmonary embolism |
Hypoxemia |
Dyspnea |
Exertional dyspnea |
Hemothorax |
Hemoptysis |
Reduced FEV1/FVC ratio |
Restrictive ventilatory defect |
| Disease(s) Associated with ACVRL1 | |||||||||||
| hereditary hemorrhagic telangiectasia |
| Mouse Phenotypes | abnormal lung vasculature morphology |
lung hemorrhage |
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| Availability | Mouse Genotype | ||
| Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Acvrl1-cre)L1Spo/0 (conditional) |
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| Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ (conditional) |
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| Acvrl1tm2Spo/Acvrl1tm2Spo Tg(Acvrl1-cre)L1Spo/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 04/23/2024 MGI 6.23 |
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