The SLC30A10 gene homepage

General information
Gene symbol SLC30A10
Gene name solute carrier family 30, member 10
Chromosome 1
Chromosomal band q41
Imprinted Unknown
Genomic reference NG_032153.1
Transcript reference NM_018713.2
Exon/intron information NM_018713.2 exon/intron table
Associated with diseases Hypermanganesemia with dystonia, polycythemia and cirrhosis
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 30
Unique public DNA variants reported 21
Individuals with public variants 15
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created March 09, 2012
Date last updated September 15, 2020
Version SLC30A10:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_018713.2.
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
Homepage URL https://www.LOVD.nl/SLC30A10
HGNC 25355
Entrez Gene 55532
PubMed articles SLC30A10
OMIM - Gene 611146
OMIM - Diseases Hypermanganesemia with dystonia, polycythemia and cirrhosis
HGMD SLC30A10
GeneCards SLC30A10
GeneTests SLC30A10
Orphanet SLC30A10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019268 1 solute carrier family 30, member 10 NM_018713.2 NP_061183.2 30


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