|
Symbol Name ID |
Mcoln1
mucolipin 1 MGI:1890498 |
| Darker colors indicate more annotations |
| Human Phenotypes | Corneal opacity |
Abnormality of retinal pigmentation |
Retinopathy |
Abnormal electroretinogram |
Strabismus |
Nystagmus |
Photophobia |
| Disease(s) Associated with MCOLN1 | |||||||
| mucolipidosis type IV |
| Mouse Phenotypes | abnormal optic nerve morphology |
thin retina inner nuclear layer |
thin retina inner plexiform layer |
abnormal retina outer nuclear layer morphology |
retina degeneration |
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| Availability | Mouse Genotype | |||||
| Mcoln1tm1Sasl/Mcoln1tm1Sasl | ||||||
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 07/02/2024 MGI 6.13 |
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