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Symbol Name ID |
Slc6a8
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 MGI:2147834 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties in infancy |
Reduced social reciprocity |
Aggressive behavior |
Attention deficit hyperactivity disorder |
Motor stereotypy |
| Disease(s) Associated with SLC6A8 | |||||
| cerebral creatine deficiency syndrome 1 |
| Mouse Phenotypes | behavior/neurological phenotype |
impaired contextual conditioning behavior |
abnormal motor learning |
abnormal object recognition memory |
impaired long-term object recognition memory |
impaired short-term object recognition memory |
abnormal spatial learning |
impaired spatial learning |
abnormal spatial reference memory |
abnormal spatial working memory |
abnormal response to novel object |
increased grooming behavior |
impaired coordination |
impaired swimming |
decreased grip strength |
decreased locomotor activity |
hyperactivity |
decreased aerobic running capacity |
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| Availability | Mouse Genotype | ||||||||||||||||||
| Slc6a8tm1.2Clar/Y | * | ||||||||||||||||||
| Slc6a8tm1.2Lbar/Y | |||||||||||||||||||
| Slc6a8tm1e(KOMP)Wtsi/Y | |||||||||||||||||||
| Slc6a8tm1.1Clar/Y Tg(Camk2a-cre)2Gsc/0 (conditional) |
* | ||||||||||||||||||
| Slc6a8tm1.1Lbar/Y Tg(Nes-cre)1Kln/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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