Symbol Name ID |
Mks1
MKS transition zone complex subunit 1 MGI:3584243 |
Darker colors indicate more annotations |
Human Phenotypes | Astigmatism |
Cataract |
Retinal dystrophy |
Cone/cone-rod dystrophy |
Hypertelorism |
Abnormal electroretinogram |
Strabismus |
Nystagmus |
Color vision defect |
Nyctalopia |
Photophobia |
Reduced visual acuity |
Blindness |
Disease(s) Associated with MKS1 | |||||||||||||
Bardet-Biedl syndrome |
Mouse Phenotypes | abnormal eye morphology |
enophthalmos |
ocular hypertelorism |
microphthalmia |
anophthalmia |
|
Availability | Mouse Genotype | |||||
Mks1hlb614/Mks1hlb614 | ||||||
Mks1tm1a(EUCOMM)Wtsi/Mks1tm1a(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 07/02/2024 MGI 6.13 |
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