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Gene Info

Gene Information For:Hs. SLC6A8, Solute carrier family 6 (neurotransmitter transporter, creatine), member 8
Sequence ID:NM_005629
NM_001142805
NM_001142806
RefSeqGene ID:NG_012016
Entrez Gene ID:6535
Ensembl ID:ENSG00000130821

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaDTPSNPSNP: GeneViewSNP: VarViewAssembliesRNAi

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
CREATINE DEFICIENCY SYNDROME, X-LINKED 

Cytogenetic Location (from UniGene)

Cytogenetic Location:Xq28Mitelman Breakpoint Data

Chromosomal Position (from UCSC)

Chromosomal Position:X: 152953947 - 152960858

 Exon Info From UCSC:
NM_005629
NM_001142805
NM_001142806

Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
4634609Full LengthBC012355solute carrier family 6 (neurotransmitter transporter, creatine), member 8
4823748Full LengthBC081558solute carrier family 6 (neurotransmitter transporter, creatine), member 8

Protein Similarities Based on Shared Motif Content

Find gene products sharing protein motifs with:  NP_005620  

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_001142805 NP_001136277    
NM_001142806 NP_001136278    
NM_005629 NP_005620 P48029 SNF

Related Sequences

 
mRNAGenPeptSwissProt
U17986 AAA86990 P48029
S74039 AAB32284 P48029
L31409 AAC41688 P48029
BC012355 AAH12355 P48029
BC081558 AAH81558 P48029
DQ892306 ABM83232  
DQ895505 ABM86431  
EU280316 ABZ82022 P48029
AB209704 BAD92941 Q59EV7
AK295495 BAG58415 B4DIA3

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens SLC6A8 NP_005620 M.musculus Slc6a8 102857 Gene Info NP_001136281 99
R.norvegicus Slc6a8 50690   NP_059044 98

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)