|
Symbol Name ID |
Slc6a8
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 MGI:2147834 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertonia |
Spasticity |
Hypotonia |
Axial hypotonia |
Neonatal hypotonia |
| Disease(s) Associated with SLC6A8 | |||||
| cerebral creatine deficiency syndrome 1 |
| Mouse Phenotypes | abnormal muscle morphology |
skeletal muscle fiber atrophy |
abnormal muscle physiology |
hypotonia |
muscle weakness |
|
| Availability | Mouse Genotype | |||||
| Slc6a8tm1e(KOMP)Wtsi/Y | ||||||
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