The SLC6A17 gene homepage

General information
Gene symbol SLC6A17
Gene name solute carrier family 6, member 17
Chromosome 1
Chromosomal band p13.2
Imprinted Unknown
Genomic reference NC_000001.10
Transcript reference NM_001010898.2
Associated with diseases MRT48
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 9
Unique public DNA variants reported 9
Individuals with public variants 2
Hidden variants 3
Date created May 03, 2013
Date last updated February 26, 2024
Version SLC6A17:240226

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
HGNC 31399
Entrez Gene 388662
PubMed articles SLC6A17
OMIM - Gene 610299
OMIM - Diseases MRT48 (mental retardation, autosomal recessive, type 48 (MRT-48))
Orphanet SLC6A17


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019050 1 solute carrier family 6, member 17 NM_001010898.2 NP_001010898.1 9


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