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Symbol Name ID |
Qrsl1
glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 MGI:1923813 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intrauterine growth retardation |
| Disease(s) Associated with QRSL1 | |
| combined oxidative phosphorylation deficiency 40 |
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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