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XB-GENEPAGE-986839
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 slc6a8

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solute carrier family 6 member 8

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( Nomenclature history )

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Sodium-neurotransmitter symporter

AI Protein Function :
slc6a8 encodes a plasma‑membrane creatine transporter that mediates sodium‑dependent uptake of creatine, supporting cellular energy buffering and osmolyte balance; it is expressed in brain, spinal cord...[+]



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Diseases: 


Disease Ontology:
cerebral creatine deficiency syndrome 1

MIM:
CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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