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Symbol Name ID |
Slc6a8
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 MGI:2147834 |
| Darker colors indicate more annotations |
| Human Phenotypes | Mandibular prognathia |
Malar flattening |
Microcephaly |
Joint hypermobility |
| Disease(s) Associated with SLC6A8 | ||||
| cerebral creatine deficiency syndrome 1 |
| Mouse Phenotypes | kyphosis |
kyphoscoliosis |
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| 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) |
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last database update 04/16/2024 MGI 6.23 |
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