|
Symbol Name ID |
Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8 MGI:1919241 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal hemorrhage |
Retinal arteriolar constriction |
Conjunctivitis |
Keratoconjunctivitis sicca |
Abnormal eye morphology |
Abnormal cornea morphology |
Corneal ulceration |
Opacification of the corneal stroma |
Band keratopathy |
Lentiglobus |
Cataract |
Developmental cataract |
Optic atrophy |
Optic disc pallor |
Abnormality of retinal pigmentation |
Pigmentary retinopathy |
Retinal pigment epithelial mottling |
Retinal degeneration |
Retinal atrophy |
Retinal dystrophy |
Uveitis |
Deeply set eye |
Anophthalmia |
Microphthalmia |
Miosis |
Abnormal electroretinogram |
Abnormality of visual evoked potentials |
Strabismus |
Nystagmus |
Hypermetropia |
Photophobia |
Visual impairment |
Progressive visual loss |
Decreased lacrimation |
Alacrima |
| Disease(s) Associated with ERCC8 | |||||||||||||||||||||||||||||||||||
| Cockayne syndrome | |||||||||||||||||||||||||||||||||||
| Cockayne syndrome A |
| Mouse Phenotypes | photophobia |
retina photoreceptor degeneration |
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| Availability | Mouse Genotype | ||
| Ercc8tm1Jhjh/Ercc8tm1Jhjh | |||
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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