|
Symbol Name ID |
Trex1
three prime repair exonuclease 1 MGI:1328317 |
| Darker colors indicate more annotations |
| Human Phenotypes | Weakness of facial musculature |
Limb hypertonia |
Myositis |
Flexion contracture |
Multiple joint contractures |
Hypertonia |
Rigidity |
Extrapyramidal muscular rigidity |
Spasticity |
Lower limb spasticity |
Spastic paraparesis |
Spastic paraplegia |
Spastic tetraparesis |
Spastic tetraplegia |
Hypotonia |
Axial hypotonia |
Generalized hypotonia |
Difficulty walking |
Muscle stiffness |
Poor head control |
| Disease(s) Associated with TREX1 | ||||||||||||||||||||
| Aicardi-Goutieres syndrome | ||||||||||||||||||||
| retinal vasculopathy with cerebral leukodystrophy |
| Mouse Phenotypes | abnormal myocardial fiber morphology |
myocardial fiber degeneration |
cardiomyopathy |
myositis |
|
| Availability | Mouse Genotype | ||||
| 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 04/23/2024 MGI 6.23 |
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