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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 |
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| 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) |
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last database update 08/02/2024 MGI 6.24 |
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