|
Symbol Name ID |
Tulp1
TUB like protein 1 MGI:109571 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal arteriolar constriction |
Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Peripapillary atrophy |
Dull foveal reflex |
Abnormality of retinal pigmentation |
Pigmentary retinopathy |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Rod-cone dystrophy |
Slow pupillary light response |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
Impaired smooth pursuit |
Ophthalmoplegia |
Hypermetropia |
Myopia |
Color vision defect |
Hemeralopia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Reduced visual acuity |
Blindness |
Constriction of peripheral visual field |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with TULP1 | ||||||||||||||||||||||||||||||||||
| Leber congenital amaurosis 15 | ||||||||||||||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||||||||||||||
| retinitis pigmentosa 14 |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
increased retina apoptosis |
decreased retina photoreceptor cell number |
abnormal retina photoreceptor morphology |
abnormal photoreceptor inner segment morphology |
absent photoreceptor inner segment |
short photoreceptor inner segment |
abnormal photoreceptor outer segment morphology |
absent photoreceptor outer segment |
short photoreceptor outer segment |
photoreceptor outer segment degeneration |
retina photoreceptor degeneration |
abnormal retina pigment epithelium morphology |
abnormal retina morphology |
abnormal retina neuronal layer morphology |
abnormal retina inner nuclear layer morphology |
thin retina outer nuclear layer |
retina outer nuclear layer degeneration |
abnormal retina outer plexiform layer morphology |
increased susceptibility to age-related retinal degeneration |
retina degeneration |
retina spots |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
absent visual evoked potential |
|
| Availability | Mouse Genotype | |||||||||||||||||||||||||||
| Tulp1rd18/Tulp1rd18 | ||||||||||||||||||||||||||||
| Tulp1tm1Pjn/Tulp1tm1Pjn | ||||||||||||||||||||||||||||
| Tulp1tvrm124/Tulp1tvrm124 | ||||||||||||||||||||||||||||
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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