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Symbol Name ID |
Nup62
nucleoporin 62 MGI:1351500 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Decreased light- and dark-adapted electroretinogram amplitude |
Pendular nystagmus |
Ophthalmoparesis |
| Disease(s) Associated with NUP62 | ||||
| striatonigral degeneration |
| Mouse Phenotypes | abnormal retina inner nuclear layer morphology |
decreased total retina thickness |
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| Availability | Mouse Genotype | ||
| Nup62tm1b(KOMP)Wtsi/Nup62+ | |||
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 04/16/2024 MGI 6.23 |
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