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Symbol Name ID |
Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2 MGI:95413 |
| Darker colors indicate more annotations |
| Human Phenotypes | Conjunctival telangiectasia |
Conjunctivitis |
Keratoconjunctivitis sicca |
Blepharitis |
Keratitis |
Opacification of the corneal stroma |
Microcornea |
Corneal neovascularization |
Cataract |
Developmental cataract |
Optic atrophy |
Deeply set eye |
Microphthalmia |
Neoplasm of the eye |
Strabismus |
Nystagmus |
Photophobia |
| Disease(s) Associated with ERCC2 | |||||||||||||||||
| cerebrooculofacioskeletal syndrome 2 | |||||||||||||||||
| photosensitive trichothiodystrophy 1 | |||||||||||||||||
| xeroderma pigmentosum | |||||||||||||||||
| xeroderma pigmentosum group D |
| Mouse Phenotypes | cornea opacity |
abnormal lens morphology |
lens vacuoles |
developmental cataract |
nuclear cataract |
small lens |
microphthalmia |
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| Availability | Mouse Genotype | |||||||
| Ercc2Mhdarco15/Ercc2Mhdarco15 | ||||||||
| Ercc2tm3Jhjh/Ercc2tm3Jhjh | ||||||||
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 05/14/2024 MGI 6.23 |
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