|
Symbol Name ID |
Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8 MGI:1919241 |
| Darker colors indicate more annotations |
| Human Phenotypes | Telangiectasia |
Malar rash |
Sparse hair |
Dry hair |
Fine hair |
Anhidrosis |
Hypohidrosis |
Abnormality of skin pigmentation |
Freckling |
Hypermelanotic macule |
Pigmentation anomalies of sun-exposed skin |
Dry skin |
Reduced subcutaneous adipose tissue |
Cutaneous photosensitivity |
Prematurely aged appearance |
Premature skin wrinkling |
Progeroid facial appearance |
Atypical scarring of skin |
| Disease(s) Associated with ERCC8 | ||||||||||||||||||
| Cockayne syndrome | ||||||||||||||||||
| Cockayne syndrome A | ||||||||||||||||||
| UV-sensitive syndrome |
| Mouse Phenotypes | increased sensitivity to skin irradiation |
skin photosensitivity |
|
| 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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