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Symbol Name ID |
Bbs10
Bardet-Biedl syndrome 10 MGI:1919019 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Cataract |
Retinal dystrophy |
Cone/cone-rod dystrophy |
Rod-cone dystrophy |
Hypertelorism |
Abnormal electroretinogram |
Strabismus |
Nystagmus |
Color vision defect |
Nyctalopia |
Photophobia |
Reduced visual acuity |
Blindness |
| Disease(s) Associated with BBS10 | ||||||||||||||
| Bardet-Biedl syndrome | ||||||||||||||
| Bardet-Biedl syndrome 10 |
| Mouse Phenotypes | abnormal retina apoptosis |
photoreceptor inner segment degeneration |
abnormal photoreceptor outer segment morphology |
photoreceptor outer segment degeneration |
retina photoreceptor degeneration |
retina outer nuclear layer degeneration |
decreased total retina thickness |
retina degeneration |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||||
| Bbs10tm1.2Vmar/Bbs10tm1.2Vmar | ||||||||||
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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