Symbol Name ID |
Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8 MGI:1919241 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal hemorrhage |
Anemia |
Splenomegaly |
Disease(s) Associated with ERCC8 | |||
Cockayne syndrome | |||
Cockayne syndrome A |
Mouse Phenotypes | microgliosis |
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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 04/30/2024 MGI 6.23 |
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