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Symbol
Name
ID
Ercc1
excision repair cross-complementing rodent repair deficiency, complementation group 1
MGI:95412
Phenotype annotations related to mortality/aging
!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
Availability Mouse Genotype
Ercc1tm1Dwm/Ercc1tm1Dwm
Ercc1tm1Dwm/Ercc1tm1Dwm
Tg(Ttr-Ercc1)17Dwm/0
Ercc1tm1Jhjh/Ercc1tm1Jhjh
Ercc1tm2Jhjh/Ercc1tm2Jhjh ! !

Contributing Projects:
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
The Jackson Laboratory