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Symbol Name ID |
Whrn
whirlin MGI:2682003 |
| Darker colors indicate more annotations |
| Human Phenotypes | Rod-cone dystrophy |
Nyctalopia |
| Disease(s) Associated with WHRN | ||
| Usher syndrome type 2D |
| Mouse Phenotypes | abnormal retina photoreceptor morphology |
short photoreceptor outer segment |
thin retina outer nuclear layer |
retina degeneration |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | ||||||
| Whrntm1Tili/Whrntm1Tili | |||||||
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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