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Symbol
Name
ID

Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2
MGI:95413

Phenotype annotations related to mortality/aging

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Death in childhood	Death in infancy	Sudden cardiac death
Disease(s) Associated with ERCC2	Death in childhood	Death in infancy	Sudden cardiac death
cerebrooculofacioskeletal syndrome 2
coronary artery disease
photosensitive trichothiodystrophy 1

Mouse Phenotypes		mortality/aging	premature death	embryonic lethality before implantation, complete penetrance	premature aging
Availability	Mouse Genotype	mortality/aging	premature death		premature aging
	Ercc2^tm1Jhjh/Ercc2^tm1Jhjh
	Ercc2^tm1Jmch/Ercc2^tm1Jmch
	Ercc2^{tm2(ERCC2)Jhjh}/Ercc2^{tm2(ERCC2)Jhjh}
	Ercc2^tm2Jmch/Ercc2^tm2Jmch
	Ercc2^tm3Jhjh/Ercc2^tm3Jhjh
	Ercc2^tm1Jhjh/Ercc2^{tm2(ERCC2)Jhjh}
	Ercc2^tm1Jmch/Ercc2^{tm2(ERCC2)Jhjh}	*
	Ercc2^{tm2(ERCC2)Jhjh}/Ercc2^tm2Jmch	*

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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