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 05/28/2024 MGI 6.13 |
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