The SLC11A2 gene homepage

General information
Gene symbol SLC11A2
Gene name solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2
Chromosome 12
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_021139.1
Transcript reference NM_000617.2
Associated with diseases AHMIO1
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 8
Unique public DNA variants reported 7
Individuals with public variants 0
Hidden variants -
Date created May 03, 2013
Date last updated May 09, 2022
Version SLC11A2:220509

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 10908
Entrez Gene 4891
PubMed articles SLC11A2
OMIM - Gene 600523
OMIM - Diseases AHMIO1 (anemia, hypochromic microcytic, with iron overload 1)
Orphanet SLC11A2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019097 12 transcript variant 4 NM_000617.2 NP_000608.1 8


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