The SLC39A8 gene homepage

General information
Gene symbol SLC39A8
Gene name solute carrier family 39 (zinc transporter), member 8
Chromosome 4
Chromosomal band q22-q24
Imprinted Unknown
Genomic reference NC_000004.11
Transcript reference NM_022154.5
Exon/intron information NM_022154.5 exon/intron table
Associated with diseases CDG, CDG2N
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 20
Unique public DNA variants reported 11
Individuals with public variants 19
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated September 17, 2021
Version SLC39A8:210917

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_022154.5.
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/SLC39A8
HGNC HGNC:20862
Entrez Gene 64116
PubMed articles SLC39A8
OMIM - Gene 608732
OMIM - Diseases CDG2N (glycosylation, congenital disorder of, type IIn (CDG2N))
HGMD SLC39A8
GeneCards SLC39A8
NIH Genetic Testing Registry SLC39A8
Orphanet SLC39A8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019327 4 transcript variant 1 NM_022154.5 NP_071437.3 20


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