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Symbol
Name
ID
Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2
MGI:95413
Phenotype annotations related to growth/size/body
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Splenomegaly
Hepatosplenomegaly
Peritoneal abscess
Short stature
Tall stature
Failure to thrive
Small for gestational age
Weight loss
Obesity
Growth delay
Intrauterine growth retardation
Disease(s) Associated with ERCC2
cerebrooculofacioskeletal syndrome 2
chronic myeloid leukemia
coronary artery disease
multiple myeloma
pancreatic cancer
photosensitive trichothiodystrophy 1
xeroderma pigmentosum

Mouse Phenotypes
growth/size/body region phenotype
cachexia
decreased body size
disproportionate dwarf
postnatal growth retardation
enlarged spleen
Availability Mouse Genotype
Ercc2Mhdarco15/Ercc2Mhdarco15
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh
Ercc2tm3Jhjh/Ercc2tm3Jhjh
Ercc2tm1Jhjh/Ercc2tm2(ERCC2)Jhjh
Ercc2tm1Jmch/Ercc2tm2(ERCC2)Jhjh *
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2Jmch *

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
04/23/2024
MGI 6.23
The Jackson Laboratory