Basic Information

SLC11A2

Full name: solute carrier family 11 member 2

Gene type: protein coding

HGNC ID: HGNC:10908

Gene location: 12q13.12

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/4891

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:10908

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000617.3

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P49281

AlphaFold: https://alphafold.ebi.ac.uk/entry/P49281

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/600523

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=4891

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa04142+4891

Variant resources

Gene	Disease type	Variant type	NCBI dbSNP	Alleles	Variant location
SLC11A2		Intron Variant	rs224589	T>A / T>C / T>G	chr12:51005267 (GRCh38.p13)
SLC11A2		Non Coding Transcript Variant	rs2285230	T>C	chr12:50987967 (GRCh38.p13)