The SLC16A1 gene homepage

General information
Gene symbol SLC16A1
Gene name solute carrier family 16, member 1 (monocarboxylic acid transporter 1)
Chromosome 1
Chromosomal band p12
Imprinted Unknown
Genomic reference NG_015880.1
Transcript reference NM_003051.3
Associated with diseases HHF7, MCT1D, Erythrocyte lactate transporter defect
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 16
Unique public DNA variants reported 13
Individuals with public variants 80
Hidden variants 0
Date created May 03, 2013
Date last updated September 17, 2021
Version SLC16A1:210917

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 10922
Entrez Gene 6566
PubMed articles SLC16A1
OMIM - Gene 600682
OMIM - Diseases HHF7 (Hyperinsulinemic hypoglycemia, familial, 7)
MCT1D (monocarboxylate transporter 1 deficiency (MCT-1D))
Erythrocyte lactate transporter defect
Orphanet SLC16A1

Active transcripts




NCBI ID     

NCBI Protein ID     

00019119 1 transcript variant 1 NM_003051.3 NP_003042.3 16

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