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Symbol Name ID |
Fastkd2
FAST kinase domains 2 MGI:1922869 |
| Darker colors indicate more annotations |
| Human Phenotypes | Nystagmus |
| Disease(s) Associated with FASTKD2 | |
| combined oxidative phosphorylation deficiency 44 |
| Mouse Phenotypes | abnormal eye anterior chamber depth |
decreased total retina thickness |
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| Availability | Mouse Genotype | ||
| Fastkd2tm1b(EUCOMM)Wtsi/Fastkd2tm1b(EUCOMM)Wtsi | |||
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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