Slc6a8 Gene Search Result

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1 records found for search term Slc6a8

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
733405	Slc6a8	solute carrier family 6 (neurotransmitter transporter, creatine), member 8	Enables creatine:sodium symporter activity. Predicted to be involved in several processes, including creatine transmembrane transport; protein catabolic process; and sodium ion transmembrane transport. Predicted to be located in apical plasma membrane. Predicted to be active in glutamatergic synapse ... (more) and postsynaptic membrane. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; respiratory system; and sensory organ. Used to study cerebral creatine deficiency syndrome 1. Human ortholog(s) of this gene implicated in cerebral creatine deficiency syndrome 1 and intellectual disability. Orthologous to human SLC6A8 (solute carrier family 6 member 8). [provided by Alliance of Genome Resources, Jul 2025]	X	72716739	72726108	Mouse	261	symbol , old_gene_name , PhenoGen , description	gene, protein-coding, VALIDATED [RefSeq]