Wiki-CORONA
About
Search
Browse
Data Sources
People
Funding
Advanced Search
SLC11A2
Description
solute carrier family 11 member 2
Image
GO Annotations
Cellular Component
Cell
Nucleus
Cytoplasm
Mitochondrion
Mitochondrial Outer Membrane
Lysosomal Membrane
Early Endosome
Vacuole
Plasma Membrane
Integral Component Of Plasma Membrane
Cell Surface
Membrane
Apical Plasma Membrane
Cytoplasmic Vesicle
Brush Border Membrane
Late Endosome Membrane
Apical Part Of Cell
Basal Part Of Cell
Perinuclear Region Of Cytoplasm
Recycling Endosome
Paraferritin Complex
Extracellular Vesicle
Molecular Function
Copper Ion Transmembrane Transporter Activity
Iron Ion Transmembrane Transporter Activity
Manganese Ion Transmembrane Transporter Activity
Protein Binding
Cadmium Ion Transmembrane Transporter Activity
Cobalt Ion Transmembrane Transporter Activity
Ferrous Iron Transmembrane Transporter Activity
Lead Ion Transmembrane Transporter Activity
Nickel Cation Transmembrane Transporter Activity
Solute:proton Symporter Activity
Cadmium Ion Binding
Transition Metal Ion Transmembrane Transporter Activity
Biological Process
Response To Hypoxia
Heme Biosynthetic Process
Cobalt Ion Transport
Copper Ion Transport
Iron Ion Transport
Manganese Ion Transport
Cellular Iron Ion Homeostasis
Learning Or Memory
Response To Iron Ion
Lead Ion Transport
Iron Assimilation
Iron Ion Transmembrane Transport
Copper Ion Transmembrane Transport
Nickel Cation Transmembrane Transport
Dendrite Morphogenesis
Erythrocyte Development
Multicellular Organismal Iron Ion Homeostasis
Cadmium Ion Transmembrane Transport
Manganese Ion Transmembrane Transport
Proton Transmembrane Transport
Pathways
Metal ion SLC transporters
Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1)
Iron uptake and transport
Drugs
Diseases
GWAS
Interacting Genes
2 interacting genes:
PRIM1
VPS35
Entrez ID
4891
HPRD ID
02750
Ensembl ID
ENSG00000110911
Uniprot IDs
A0A0X8GKR4
P49281
PDB IDs
5F0L
5F0M
5F0P
Enriched GO Terms of Interacting Partners
?
Tagcloud
?