SLC6A19 gene homepage

General information
Gene symbol SLC6A19
Gene name solute carrier family 6 (neutral amino acid transporter), member 19
Chromosome 5
Chromosomal band p15
Imprinted Unknown
Genomic reference NG_008282.1
Transcript reference NM_001003841.2
Associated with diseases HND, Hyperglycinuria, Iminoglycinuria
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 12
Unique public DNA variants reported 5
Individuals with public variants 0
Hidden variants 17
Date created May 03, 2013

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 27960
Entrez Gene 340024
PubMed articles SLC6A19
OMIM - Gene 608893
OMIM - Diseases HND (Hartnup disorder (HND))

Active transcripts




NCBI ID     

NCBI Protein ID     

00019052 5 solute carrier family 6 (neutral amino acid transporter), member 19 NM_001003841.2 NP_001003841.1 12

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