Symbol Name ID |
Trex1
three prime repair exonuclease 1 MGI:1328317 |
Darker colors indicate more annotations |
Human Phenotypes | Gastrointestinal hemorrhage |
Hematemesis |
Hematochezia |
Retinal hemorrhage |
Purpura |
Petechiae |
Cardiomyopathy |
Hypertrophic cardiomyopathy |
Pericardial effusion |
Pericarditis |
Cardiomegaly |
Aortic aneurysm |
Calcification of the aorta |
Moyamoya phenomenon |
Vasculitis |
Vasculitis in the skin |
Punctate vasculitis skin lesions |
Stroke |
Hypertension |
Raynaud phenomenon |
Abnormality of the hepatic vasculature |
Lymphadenopathy |
Generalized lymphadenopathy |
Splenomegaly |
Hepatosplenomegaly |
Abnormal retinal vascular morphology |
Retinal neovascularization |
Cutis marmorata |
Erythema |
Telangiectasia |
Urticaria |
Disease(s) Associated with TREX1 | |||||||||||||||||||||||||||||||
Aicardi-Goutieres syndrome | |||||||||||||||||||||||||||||||
Chilblain lupus | |||||||||||||||||||||||||||||||
retinal vasculopathy with cerebral leukodystrophy | |||||||||||||||||||||||||||||||
systemic lupus erythematosus |
Mouse Phenotypes | liver vascular congestion |
abnormal myocardial fiber morphology |
myocardial fiber degeneration |
abnormal heart morphology |
dilated heart atrium |
enlarged heart |
dilated heart ventricle |
cardiac fibrosis |
vascular inflammation |
cardiomyopathy |
congestive heart failure |
heart inflammation |
myocarditis |
|
Availability | Mouse Genotype | |||||||||||||
Trex1tm1.1Fwpe/Trex1tm1.1Fwpe | ||||||||||||||
Trex1tm1Tld/Trex1tm1Tld |
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 09/03/2024 MGI 6.24 |
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