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Symbol Name ID |
Mkks
McKusick-Kaufman syndrome MGI:1891836 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Cataract |
Pigmentary retinopathy |
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 MKKS | |||||||||||||||
| Bardet-Biedl syndrome | |||||||||||||||
| Bardet-Biedl syndrome 6 |
| Mouse Phenotypes | eyelids open at birth |
increased susceptibility to age-related retinal degeneration |
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| Availability | Mouse Genotype | ||
| MkksGt(OST367255)Lex/MkksGt(OST367255)Lex | |||
| Mkkstm1Vcs/Mkkstm1Vcs | |||
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 05/21/2024 MGI 6.23 |
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