|
Symbol Name ID |
Ttc8
tetratricopeptide repeat domain 8 MGI:1923510 |
| Darker colors indicate more annotations |
| Human Phenotypes | Attenuation of retinal blood vessels |
Astigmatism |
Cataract |
Macular degeneration |
Bone spicule pigmentation of the retina |
Retinal dystrophy |
Cone/cone-rod dystrophy |
Rod-cone dystrophy |
Hypertelorism |
Abnormal electroretinogram |
Abnormal light- and dark-adapted electroretinogram |
Strabismus |
Nystagmus |
High myopia |
Color vision defect |
Nyctalopia |
Photophobia |
Visual impairment |
Reduced visual acuity |
Blindness |
| Disease(s) Associated with TTC8 | ||||||||||||||||||||
| Bardet-Biedl syndrome | ||||||||||||||||||||
| Bardet-Biedl syndrome 8 | ||||||||||||||||||||
| retinitis pigmentosa 51 |
| Mouse Phenotypes | abnormal photoreceptor inner segment morphology |
retina degeneration |
|
| Availability | Mouse Genotype | ||
| Ttc8tm1Reed/Ttc8tm1Reed | |||
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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