Symbol Name ID |
Ctsd
cathepsin D MGI:88562 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal atrophy |
Rod-cone dystrophy |
Visual loss |
Disease(s) Associated with CTSD | |||
neuronal ceroid lipofuscinosis 10 |
Mouse Phenotypes | retina photoreceptor degeneration |
abnormal retina morphology |
blindness |
|
Availability | Mouse Genotype | |||
Ctsdtm1Cptr/Ctsdtm1Cptr |
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 |
|
|