Symbol Name ID |
Twnk
twinkle mtDNA helicase MGI:2137410 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Depression |
Dysphonia |
Fatigue |
Myalgia |
Disease(s) Associated with TWNK | ||||
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 |
Mouse Phenotypes | behavior/neurological phenotype |
impaired coordination |
|
Availability | Mouse Genotype | ||
Tg(ACTB-Twnk*)DSuom/0 | * | ||
Tg(ACTB-Twnk*A360T)HSuom/0 | * | ||
Tg(Th-Twnk*,-EGFP)2Gcor/0 |
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 04/30/2024 MGI 6.23 |
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