Symbol Name ID |
Pcx
pyruvate carboxylase MGI:97520 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Disease(s) Associated with PC | |
pyruvate carboxylase deficiency disease |
Mouse Phenotypes | growth/size/body region phenotype |
decreased lean body mass |
increased susceptibility to weight loss |
increased kidney weight |
|
Availability | Mouse Genotype | ||||
Pcxtm1b(EUCOMM)Wtsi/Pcx+ | |||||
Pcxtm1c(EUCOMM)Wtsi/Pcxtm1c(EUCOMM)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
* |
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 04/30/2024 MGI 6.23 |
|
|