|
Symbol Name ID |
Ercc4
excision repair cross-complementing rodent repair deficiency, complementation group 4 MGI:1354163 |
| Darker colors indicate more annotations |
| Human Phenotypes | Conjunctival telangiectasia |
Blepharitis |
Attenuation of retinal blood vessels |
Keratitis |
Opacification of the corneal stroma |
Astigmatism |
Corneal scarring |
Cataract |
Optic atrophy |
Deeply set eye |
Neoplasm of the eye |
Strabismus |
Nystagmus |
Photophobia |
Visual impairment |
Blindness |
| Disease(s) Associated with ERCC4 | ||||||||||||||||
| xeroderma pigmentosum | ||||||||||||||||
| xeroderma pigmentosum group F | ||||||||||||||||
| XFE progeroid syndrome |
| Mouse Phenotypes | anophthalmia |
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| Availability | Mouse Genotype | |
| Ercc4em1(IMPC)J/Ercc4em1(IMPC)J | ||
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 04/09/2024 MGI 6.23 |
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