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Symbol Name ID |
Ercc6
excision repair cross-complementing rodent repair deficiency, complementation group 6 MGI:1100494 |
| Darker colors indicate more annotations |
| Human Phenotypes | Deep longitudinal plantar crease |
Wide intermamillary distance |
Telangiectasia |
Malar rash |
Abnormal hair morphology |
Hirsutism |
Sparse hair |
Dry hair |
Fine hair |
Anhidrosis |
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 |
Dermal atrophy |
Atypical scarring of skin |
Poikiloderma |
Parakeratosis |
| Disease(s) Associated with ERCC6 | ||||||||||||||||||||||||
| cerebrooculofacioskeletal syndrome 1 | ||||||||||||||||||||||||
| Cockayne syndrome | ||||||||||||||||||||||||
| Cockayne syndrome B | ||||||||||||||||||||||||
| De Sanctis-Cacchione syndrome | ||||||||||||||||||||||||
| UV-sensitive syndrome |
| Mouse Phenotypes | skin photosensitivity |
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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 04/16/2024 MGI 6.23 |
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