The SLC6A8 gene homepage

General information
Gene symbol SLC6A8
Gene name solute carrier family 6 (neurotransmitter transporter), member 8
Chromosome X
Chromosomal band q28
Imprinted Unknown
Genomic reference NG_012016.1
Transcript reference NM_001142805.1, NM_001142806.1, NM_005629.3
Associated with diseases CCDS-1, ID
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 21
Unique public DNA variants reported 8
Individuals with public variants 17
Hidden variants -
Date created December 09, 2013
Date last updated September 23, 2016
Version SLC6A8:160923

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:11055
Entrez Gene 6535
PubMed articles SLC6A8
OMIM - Gene 300036
OMIM - Diseases CCDS-1 (creatine deficiency syndrome, cerebral, type 1 (CCDS-1))
HGMD SLC6A8
GeneCards SLC6A8
GeneTests SLC6A8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024161 X Manually created transcript NM_005629.3 - 21
00027610 X Manually created transcript NM_001142806.1 - 21
00023665 X Manually created transcript NM_001142805.1 - 20


Copyright & disclaimer
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