Symbol Name ID |
Ercc1
excision repair cross-complementing rodent repair deficiency, complementation group 1 MGI:95412 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Death in childhood |
Disease(s) Associated with ERCC1 | |
cerebrooculofacioskeletal syndrome 4 |
Mouse Phenotypes | increased susceptibility to xenobiotic induced morbidity/mortality |
lethality at weaning, complete penetrance |
premature death |
postnatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
embryonic lethality during organogenesis, incomplete penetrance |
premature aging |
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Availability | Mouse Genotype | |||||||
Ercc1tm1Dwm/Ercc1tm1Dwm | ||||||||
Ercc1tm1Dwm/Ercc1tm1Dwm Tg(Ttr-Ercc1)17Dwm/0 |
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Ercc1tm1Jhjh/Ercc1tm1Jhjh | ||||||||
Ercc1tm2Jhjh/Ercc1tm2Jhjh | ! | ! |
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 09/03/2024 MGI 6.24 |
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