Symbol Name ID |
Ercc6
excision repair cross-complementing rodent repair deficiency, complementation group 6 MGI:1100494 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Delayed puberty |
Severe short stature |
Failure to thrive |
Severe failure to thrive |
Small for gestational age |
Cachexia |
Growth delay |
Intrauterine growth retardation |
Postnatal growth retardation |
Disease(s) Associated with ERCC6 | |||||||||||
cerebrooculofacioskeletal syndrome 1 | |||||||||||
Cockayne syndrome | |||||||||||
Cockayne syndrome B | |||||||||||
De Sanctis-Cacchione syndrome |
Mouse Phenotypes | decreased body weight |
postnatal growth retardation |
|
Availability | Mouse Genotype | ||
Ercc6tm1Gvh/Ercc6tm1Gvh |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/14/2024 MGI 6.23 |
|
|