Entity Details

Primary name S40A1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NP59
EntryNameS40A1_HUMAN
FullNameSolute carrier family 40 member 1
TaxID9606
Evidenceevidence at protein level
Length571
SequenceStatuscomplete
DateCreated2004-06-07
DateModified2021-06-02

Ontological Relatives

GenesSLC40A1

GO terms

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GOName
GO:0005381 iron ion transmembrane transporter activity
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0006879 cellular iron ion homeostasis
GO:0015093 ferrous iron transmembrane transporter activity
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0017046 peptide hormone binding
GO:0034755 iron ion transmembrane transport
GO:0055072 iron ion homeostasis
GO:0060586 multicellular organismal iron ion homeostasis
GO:1903988 iron ion export across plasma membrane

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR009716 Ferroportin-1FamilyFamily
IPR036259 MFS transporter superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
606069 OMIMHemochromatosis 4 (HFE4)A disorder of iron metabolism characterized by iron overload. Excess iron is deposited in a variety of organs leading to their failure, and resulting in serious illnesses including cirrhosis, hepatomas, diabetes, cardiomyopathy, arthritis, and hypogonadotropic hypogonadism. Severe effects of the disease usually do not appear until after decades of progressive iron loading. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB13257 Ferrous sulfate anhydrousDrugbanksmall molecule
DB14520 Tetraferric tricitrate decahydrateDrugbanksmall molecule