|
Symbol Name ID |
Pex13
peroxisomal biogenesis factor 13 MGI:1919379 |
| Darker colors indicate more annotations |
| Human Phenotypes | Infantile muscular hypotonia |
Severe muscular hypotonia |
| Disease(s) Associated with PEX13 | ||
| peroxisome biogenesis disorder 11A |
| Mouse Phenotypes | hypotonia |
|
| Availability | Mouse Genotype | |
| Pex13tm1.1Crne/Pex13tm1.1Crne | ||
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 |
|
|
|
||
Analysis Tools