|
Symbol Name ID |
Slc25a46
solute carrier family 25, member 46 MGI:1914703 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
| Disease(s) Associated with SLC25A46 | |
| pontocerebellar hypoplasia type 1E |
| Mouse Phenotypes | decreased amacrine cell number |
abnormal retina ganglion cell morphology |
optic nerve atrophy |
|
| Availability | Mouse Genotype | |||
| Slc25a46atc/Slc25a46atc | ||||
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