Symbol Name ID |
Ercc6
excision repair cross-complementing rodent repair deficiency, complementation group 6 MGI:1100494 |
Darker colors indicate more annotations |
Human Phenotypes | Conjunctivitis |
Keratoconjunctivitis sicca |
Splenomegaly |
Keratitis |
Uveitis |
Malar rash |
Recurrent pneumonia |
Disease(s) Associated with ERCC6 | |||||||
cerebrooculofacioskeletal syndrome 1 | |||||||
Cockayne syndrome | |||||||
Cockayne syndrome B | |||||||
De Sanctis-Cacchione syndrome |
Mouse Phenotypes | microgliosis |
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Availability | Mouse Genotype | |
Ercc6tm1Gvh/Ercc6tm1Gvh |
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 05/28/2024 MGI 6.13 |
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