Symbol Name ID |
Slc32a1
solute carrier family 32 (GABA vesicular transporter), member 1 MGI:1194488 |
Darker colors indicate more annotations |
Human Phenotypes | Autistic behavior |
Obsessive-compulsive trait |
Disease(s) Associated with SLC32A1 | ||
generalized epilepsy with febrile seizures plus |
Mouse Phenotypes | abnormal food intake |
hunched posture |
increased locomotor activity |
no spontaneous movement |
increased kindling response |
tonic-clonic seizures |
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Availability | Mouse Genotype | ||||||
Slc32a1tm1.1Bgc/Slc32a1tm1.1Bgc | |||||||
Slc32a1tm1Bros/Slc32a1tm1Bros | |||||||
Slc32a1tm2(cre)Lowl/Slc32a1tm2(cre)Lowl | |||||||
Agrptm1(cre)Lowl/Agrp+ Slc32a1tm1Lowl/Slc32a1tm1Lowl (conditional) |
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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