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Symbol Name ID |
Ptpn22
protein tyrosine phosphatase, non-receptor type 22 (lymphoid) MGI:107170 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal arteritis |
Keratoconjunctivitis sicca |
Abnormality of the cardiovascular system |
Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis |
Pericarditis |
Abdominal aortic aneurysm |
Aortic dissection |
Premature coronary artery atherosclerosis |
Vasculitis |
Hypertension |
Raynaud phenomenon |
Cerebral ischemia |
Arrhythmia |
Sudden cardiac death |
Tachycardia |
Myocardial infarction |
Congestive heart failure |
Lymphadenopathy |
Mediastinal lymphadenopathy |
Thymoma |
Hepatosplenomegaly |
Erythema |
Telangiectasia |
| Disease(s) Associated with PTPN22 | |||||||||||||||||||||||
| Addison's disease | |||||||||||||||||||||||
| Behcet's disease | |||||||||||||||||||||||
| coronary artery disease | |||||||||||||||||||||||
| graft-versus-host disease | |||||||||||||||||||||||
| Graves' disease | |||||||||||||||||||||||
| myasthenia gravis | |||||||||||||||||||||||
| rheumatoid arthritis | |||||||||||||||||||||||
| Sjogren's syndrome | |||||||||||||||||||||||
| systemic lupus erythematosus | |||||||||||||||||||||||
| systemic scleroderma | |||||||||||||||||||||||
| temporal arteritis |
| Mouse Phenotypes | vascular inflammation |
|
| Availability | Mouse Genotype | |
| Ptpn22tm1.1Draw/Ptpn22tm1.1Draw | ||
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 05/21/2024 MGI 6.23 |
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