|
Symbol Name ID |
Pcca
propionyl-Coenzyme A carboxylase, alpha polypeptide MGI:97499 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hyperglycinemia |
Hyperammonemia |
Propionyl-CoA carboxylase deficiency |
Hypoglycemia |
Lactic acidosis |
Metabolic acidosis |
Dehydration |
Increased level of hippuric acid in urine |
Hyperglycinuria |
| Disease(s) Associated with PCCA | |||||||||
| propionic acidemia |
| Mouse Phenotypes | dehydration |
decreased liver glycogen level |
ketoaciduria |
|
| Availability | Mouse Genotype | |||
| Pccatm1Tmiy/Pccatm1Tmiy | ||||
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 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools