Symbol Name ID |
Trex1
three prime repair exonuclease 1 MGI:1328317 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal hemorrhage |
Macular edema |
Abnormal retinal vascular morphology |
Retinal neovascularization |
Developmental glaucoma |
Retinopathy |
Retinal cotton wool spot |
Retinal exudate |
Abnormality of eye movement |
Strabismus |
Nystagmus |
Visual impairment |
Visual field defect |
Hemianopia |
Progressive visual loss |
Glaucoma |
Ptosis |
Disease(s) Associated with TREX1 | |||||||||||||||||
Aicardi-Goutieres syndrome | |||||||||||||||||
retinal vasculopathy with cerebral leukodystrophy | |||||||||||||||||
systemic lupus erythematosus |
Mouse Phenotypes | lacrimal gland inflammation |
|
Availability | Mouse Genotype | |
Trex1tm1.1Fwpe/Trex1tm1.1Fwpe |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 09/03/2024 MGI 6.24 |
![]() |
|