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Symbol Name ID |
Ush1c
USH1 protein network component harmonin MGI:1919338 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Cataract |
Iris hypopigmentation |
Abnormality of retinal pigmentation |
Rod-cone dystrophy |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
High hypermetropia |
Myopia |
Nyctalopia |
Visual impairment |
Blindness |
Visual field defect |
Hemianopia |
Scotoma |
Visual loss |
Progressive visual loss |
| Disease(s) Associated with USH1C | ||||||||||||||||||
| Usher syndrome | ||||||||||||||||||
| Usher syndrome type 1 | ||||||||||||||||||
| Usher syndrome type 1C |
| Mouse Phenotypes | vision/eye phenotype |
retina degeneration |
abnormal electroretinogram waveform feature |
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| Availability | Mouse Genotype | |||
| Ush1cdfcr-3J/Ush1cdfcr-3J | * | |||
| Ush1cdfcr/Ush1cdfcr | ||||
| Ush1ctm1Xzl/Ush1ctm1Xzl | * | |||
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 04/30/2024 MGI 6.23 |
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