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Symbol Name ID |
Bbs5
Bardet-Biedl syndrome 5 MGI:1919819 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Cataract |
Macular dystrophy |
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 BBS5 | |||||||||||||||
| Bardet-Biedl syndrome | |||||||||||||||
| Bardet-Biedl syndrome 5 |
| Mouse Phenotypes | abnormal retina morphology |
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| Availability | Mouse Genotype | |
| Bbs5tm1b(EUCOMM)Wtsi/Bbs5tm1b(EUCOMM)Wtsi | ||
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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