The SLC46A1 gene homepage

General information
Gene symbol SLC46A1
Gene name solute carrier family 46 (folate transporter), member 1
Chromosome 17
Chromosomal band q11.2
Imprinted Unknown
Genomic reference LRG_183
Transcript reference NM_080669.4
Associated with diseases folate malabsorption, hereditary
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 38
Unique public DNA variants reported 33
Individuals with public variants 85
Hidden variants 3
Date created May 03, 2013
Date last updated July 07, 2023
Version SLC46A1:230707

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 30521
Entrez Gene 113235
PubMed articles SLC46A1
OMIM - Gene 611672
OMIM - Diseases folate malabsorption, hereditary
Orphanet SLC46A1

Active transcripts




NCBI ID     

NCBI Protein ID     

00019350 17 transcript variant 1 NM_080669.4 NP_542400.2 38

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