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Symbol Name ID |
Ercc4
excision repair cross-complementing rodent repair deficiency, complementation group 4 MGI:1354163 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hepatosplenomegaly |
Ascites |
Peritoneal abscess |
Short stature |
Severe short stature |
Decreased body weight |
Failure to thrive |
Weight loss |
Cachexia |
Growth delay |
| Disease(s) Associated with ERCC4 | ||||||||||
| Fanconi anemia complementation group Q | ||||||||||
| pancreatic cancer | ||||||||||
| xeroderma pigmentosum | ||||||||||
| xeroderma pigmentosum group F | ||||||||||
| XFE progeroid syndrome |
| Mouse Phenotypes | decreased body weight |
postnatal growth retardation |
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| Availability | Mouse Genotype | ||
| Ercc4tm1Fwa/Ercc4tm1Fwa | |||
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 04/09/2024 MGI 6.23 |
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