Symbol Name ID |
Sprtn
SprT-like N-terminal domain MGI:2685351 |
Darker colors indicate more annotations |
Human Phenotypes | Cataract |
Posterior subcapsular cataract |
Disease(s) Associated with SPRTN | ||
Ruijs-Aalfs syndrome |
Mouse Phenotypes | cataract |
|
Availability | Mouse Genotype | |
Sprtntm1Yjm/Sprtntm1Yjm |
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 |
|
|