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Symbol Name ID |
Tlcd3b
TLC domain containing 3B MGI:1916202 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of retinal pigmentation |
Color vision defect |
Nyctalopia |
Photophobia |
Visual impairment |
| Disease(s) Associated with TLCD3B | |||||
| cone-rod dystrophy |
| Mouse Phenotypes | decreased retina cone cell number |
abnormal retina morphology |
abnormal retina outer nuclear layer morphology |
thin retina outer nuclear layer |
decreased total retina thickness |
decreased b-wave amplitude |
abnormal cone electrophysiology |
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| Availability | Mouse Genotype | |||||||
| Tlcd3bem1(IMPC)Bay/Tlcd3bem1(IMPC)Bay | ||||||||
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 05/28/2024 MGI 6.13 |
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