Symbol Name ID |
Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2 MGI:95413 |
* | 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 | * |
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 |
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