Symbol Name ID |
Ercc4
excision repair cross-complementing rodent repair deficiency, complementation group 4 MGI:1354163 |
Darker colors indicate more annotations |
Human Phenotypes | Chromosome breakage |
Defective DNA repair after ultraviolet radiation damage |
Deficient excision of UV-induced pyrimidine dimers in DNA |
Hypoalbuminemia |
Elevated circulating hepatic transaminase concentration |
Diabetes mellitus |
Fever |
Proteinuria |
Aminoaciduria |
Ascites |
Corneal scarring |
Disease(s) Associated with ERCC4 | |||||||||||
Fanconi anemia complementation group Q | |||||||||||
pancreatic cancer | |||||||||||
xeroderma pigmentosum | |||||||||||
xeroderma pigmentosum group F | |||||||||||
XFE progeroid syndrome |
Mouse Phenotypes | abnormal DNA repair |
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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 04/16/2024 MGI 6.23 |
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