Symbol Name ID |
Slc1a4
solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 MGI:2135601 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Gastrostomy tube feeding in infancy |
Urinary incontinence |
Hyperactivity |
Motor stereotypy |
Hair-pulling |
Disease(s) Associated with SLC1A4 | |||||
spastic tetraplegia, thin corpus callosum, and progressive microcephaly |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal response to novel object |
|
Availability | Mouse Genotype | ||
Slc1a4em2Tmg/Slc1a4em2Tmg | * |
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 |
![]() |
|