|
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 |
|
|
|
||
Analysis Tools