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Symbol Name ID |
Timm22
translocase of inner mitochondrial membrane 22 MGI:1929742 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties in infancy |
| Disease(s) Associated with TIMM22 | |
| combined oxidative phosphorylation deficiency 43 |
| Mouse Phenotypes | hyperactivity |
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| Availability | Mouse Genotype | |
| Timm22tm1b(KOMP)Wtsi/Timm22+ | ||
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 04/09/2024 MGI 6.23 |
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