SLC39A4 gene homepage

General information
Gene symbol SLC39A4
Gene name solute carrier family 39 (zinc transporter), member 4
Chromosome 8
Chromosomal band q24.3
Imprinted Unknown
Genomic reference NG_012234.2
Transcript reference NM_017767.2, NM_130849.2
Exon/intron information NM_130849.2 exon/intron table
Associated with diseases acrodermatitis enteropathica, Zinc deficiency (AEZ)
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Sébastien Küry
Total number of public variants reported 24
Unique public DNA variants reported 18
Individuals with public variants 22
Hidden variants 0
Download all this gene's data Download all data
Date created May 03, 2013
Date last updated January 23, 2015
Version SLC39A4:150123

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_130849.2.
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 http://www.LOVD.nl/SLC39A4
HGNC 17129
Entrez Gene 55630
PubMed articles SLC39A4
OMIM - Gene 607059
OMIM - Diseases acrodermatitis enteropathica, Zinc deficiency (AEZ)
HGMD SLC39A4
GeneCards SLC39A4
GeneTests SLC39A4


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024005 8 transcript variant 2 NM_130849.2 NP_570901.2 24
00024014 8 transcript variant 1 NM_017767.2 NP_060237.2 13


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