Symbol Name ID |
Slc17a5
solute carrier family 17 (anion/sugar transporter), member 5 MGI:1924105 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertelorism |
Exotropia |
Nystagmus |
Disease(s) Associated with SLC17A5 | |||
sialuria |
Mouse Phenotypes | abnormal optic nerve morphology |
|
Availability | Mouse Genotype | |
Slc17a5tm1Lex/Slc17a5tm1Lex |
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 08/02/2024 MGI 6.24 |
|
|