Symbol Name ID |
Twnk
twinkle mtDNA helicase MGI:2137410 |
Darker colors indicate more annotations |
Human Phenotypes | Elevated circulating alanine aminotransferase concentration |
Elevated circulating aspartate aminotransferase concentration |
Diabetes mellitus |
Increased circulating lactate concentration |
Elevated circulating follicle stimulating hormone level |
Elevated circulating luteinizing hormone level |
Increased circulating gonadotropin level |
Decreased serum estradiol |
Exercise intolerance |
Disease(s) Associated with TWNK | |||||||||
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | |||||||||
mitochondrial DNA depletion syndrome 7 | |||||||||
Perrault syndrome |
Mouse Phenotypes | abnormal autophagy |
abnormal DNA repair |
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Availability | Mouse Genotype | ||
Tg(ACTB-Twnk*)DSuom/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 08/02/2024 MGI 6.24 |
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