Ferroportin: Difference between revisions

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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{protein
{{PBB_Controls
|Name=solute carrier family 40 (iron-regulated transporter), member 1
| update_page = yes
|caption=
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|HGNCid=10909
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|Symbol=SLC40A1
}}
|AltSymbols=SLC11A3 FPN1

|EntrezGene=30061
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
|OMIM=604653
{{GNF_Protein_box
|RefSeq=NM_014585
| image =
|UniProt=Q9NP59
| image_source =
|PDB=
| PDB =
|ECnumber=
| Name = Solute carrier family 40 (iron-regulated transporter), member 1
|Chromosome=2
| HGNCid = 10909
|Arm=q
| Symbol = SLC40A1
|Band=32
| AltSymbols =; FPN1; HFE4; IREG1; MST079; MSTP079; MTP1; SLC11A3
|LocusSupplementaryData=
| OMIM = 604653
| ECnumber =
| Homologene = 40959
| MGIid = 1315204
| Function = {{GNF_GO|id=GO:0005381 |text = iron ion transmembrane transporter activity}} {{GNF_GO|id=GO:0005506 |text = iron ion binding}}
| Component = {{GNF_GO|id=GO:0005737 |text = cytoplasm}} {{GNF_GO|id=GO:0005886 |text = plasma membrane}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0008021 |text = synaptic vesicle}}
| Process = {{GNF_GO|id=GO:0006811 |text = ion transport}} {{GNF_GO|id=GO:0006826 |text = iron ion transport}} {{GNF_GO|id=GO:0006879 |text = cellular iron ion homeostasis}} {{GNF_GO|id=GO:0009653 |text = anatomical structure morphogenesis}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 30061
| Hs_Ensembl = ENSG00000138449
| Hs_RefseqProtein = NP_055400
| Hs_RefseqmRNA = NM_014585
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 2
| Hs_GenLoc_start = 190133563
| Hs_GenLoc_end = 190153858
| Hs_Uniprot = Q9NP59
| Mm_EntrezGene = 53945
| Mm_Ensembl = ENSMUSG00000025993
| Mm_RefseqmRNA = NM_016917
| Mm_RefseqProtein = NP_058613
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 1
| Mm_GenLoc_start = 45852630
| Mm_GenLoc_end = 45870079
| Mm_Uniprot = Q3TJ33
}}
}}
}}
'''Ferroportin''' is a [[transmembrane protein]] that transports [[iron]] from the inside of a [[cell (biology)|cell]] to the outside of it. It is found on the surface of cells that store or transport iron, including:
'''Ferroportin''' is a [[transmembrane protein]] that transports [[iron]] from the inside of a [[cell (biology)|cell]] to the outside of it. It is found on the surface of cells that store or transport iron, including:
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==Clinical significance==
==Clinical significance==
Ferroportin can be associated with [[African iron overload]].
Ferroportin can be associated with [[African iron overload]].

==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Pietrangelo A |title=The ferroportin disease. |journal=Blood Cells Mol. Dis. |volume=32 |issue= 1 |pages= 131-8 |year= 2004 |pmid= 14757427 |doi= }}
*{{cite journal | author=Robson KJ, Merryweather-Clarke AT, Cadet E, ''et al.'' |title=Recent advances in understanding haemochromatosis: a transition state. |journal=J. Med. Genet. |volume=41 |issue= 10 |pages= 721-30 |year= 2005 |pmid= 15466004 |doi= 10.1136/jmg.2004.020644 }}
*{{cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171-4 |year= 1994 |pmid= 8125298 |doi= }}
*{{cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149-56 |year= 1997 |pmid= 9373149 |doi= }}
*{{cite journal | author=Donovan A, Brownlie A, Zhou Y, ''et al.'' |title=Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter. |journal=Nature |volume=403 |issue= 6771 |pages= 776-81 |year= 2000 |pmid= 10693807 |doi= 10.1038/35001596 }}
*{{cite journal | author=Abboud S, Haile DJ |title=A novel mammalian iron-regulated protein involved in intracellular iron metabolism. |journal=J. Biol. Chem. |volume=275 |issue= 26 |pages= 19906-12 |year= 2000 |pmid= 10747949 |doi= 10.1074/jbc.M000713200 }}
*{{cite journal | author=Haile DJ |title=Assignment of Slc11a3 to mouse chromosome 1 band 1B and SLC11A3 to human chromosome 2q32 by in situ hybridization. |journal=Cytogenet. Cell Genet. |volume=88 |issue= 3-4 |pages= 328-9 |year= 2000 |pmid= 10828623 |doi= }}
*{{cite journal | author=McKie AT, Marciani P, Rolfs A, ''et al.'' |title=A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation. |journal=Mol. Cell |volume=5 |issue= 2 |pages= 299-309 |year= 2000 |pmid= 10882071 |doi= }}
*{{cite journal | author=Hartley JL, Temple GF, Brasch MA |title=DNA cloning using in vitro site-specific recombination. |journal=Genome Res. |volume=10 |issue= 11 |pages= 1788-95 |year= 2001 |pmid= 11076863 |doi= }}
*{{cite journal | author=Wiemann S, Weil B, Wellenreuther R, ''et al.'' |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422-35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.154701 }}
*{{cite journal | author=Simpson JC, Wellenreuther R, Poustka A, ''et al.'' |title=Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. |journal=EMBO Rep. |volume=1 |issue= 3 |pages= 287-92 |year= 2001 |pmid= 11256614 |doi= 10.1093/embo-reports/kvd058 }}
*{{cite journal | author=Njajou OT, Vaessen N, Joosse M, ''et al.'' |title=A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. |journal=Nat. Genet. |volume=28 |issue= 3 |pages= 213-4 |year= 2001 |pmid= 11431687 |doi= 10.1038/90038 }}
*{{cite journal | author=Montosi G, Donovan A, Totaro A, ''et al.'' |title=Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. |journal=J. Clin. Invest. |volume=108 |issue= 4 |pages= 619-23 |year= 2001 |pmid= 11518736 |doi= }}
*{{cite journal | author=Press RD |title=Hemochromatosis caused by mutations in the iron-regulatory proteins ferroportin and H ferritin. |journal=Mol. Diagn. |volume=6 |issue= 4 |pages= 347 |year= 2002 |pmid= 11774199 |doi= }}
*{{cite journal | author=Lee PL, Gelbart T, West C, ''et al.'' |title=A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin. |journal=Blood Cells Mol. Dis. |volume=27 |issue= 5 |pages= 783-802 |year= 2003 |pmid= 11783942 |doi= 10.1006/bcmd.2001.0445 }}
*{{cite journal | author=Rolfs A, Bonkovsky HL, Kohlroser JG, ''et al.'' |title=Intestinal expression of genes involved in iron absorption in humans. |journal=Am. J. Physiol. Gastrointest. Liver Physiol. |volume=282 |issue= 4 |pages= G598-607 |year= 2002 |pmid= 11897618 |doi= 10.1152/ajpgi.00371.2001 }}
*{{cite journal | author=Thomas C, Oates PS |title=IEC-6 cells are an appropriate model of intestinal iron absorption in rats. |journal=J. Nutr. |volume=132 |issue= 4 |pages= 680-7 |year= 2002 |pmid= 11925460 |doi= }}
*{{cite journal | author=Wallace DF, Pedersen P, Dixon JL, ''et al.'' |title=Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis. |journal=Blood |volume=100 |issue= 2 |pages= 692-4 |year= 2002 |pmid= 12091366 |doi= }}
*{{cite journal | author=Devalia V, Carter K, Walker AP, ''et al.'' |title=Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). |journal=Blood |volume=100 |issue= 2 |pages= 695-7 |year= 2002 |pmid= 12091367 |doi= 10.1182/blood-2001-11-0132 }}
*{{cite journal | author=Roetto A, Merryweather-Clarke AT, Daraio F, ''et al.'' |title=A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. |journal=Blood |volume=100 |issue= 2 |pages= 733-4 |year= 2002 |pmid= 12123233 |doi= }}
}}
{{refend}}


==External links==
==External links==
* {{MeshName|ferroportin1+protein}}
* {{MeshName|ferroportin1+protein}}


{{membrane-protein-stub}}
{{Membrane transport proteins}}
{{Membrane transport proteins}}


[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Transmembrane proteins]]
[[Category:Metabolism]]
[[Category:Metabolism]]
[[Category:Transport proteins]]

[[Category:Transmembrane proteins]]
{{membrane-protein-stub}}


[[de:Ferroportin]]
[[de:Ferroportin]]

Revision as of 17:34, 19 January 2008

Template:PBB Controls

SLC40A1
Identifiers
AliasesSLC40A1, IREG1, MST079, MSTP079, solute carrier family 40 member 1, MTP1, SLC11A3, FPN1, HFE4
External IDsOMIM: 604653 MGI: 1315204 HomoloGene: 40959 GeneCards: SLC40A1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014585

NM_016917

RefSeq (protein)

NP_055400

NP_058613

Location (UCSC)Chr 2: 189.56 – 189.58 MbChr 1: 45.95 – 45.97 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Ferroportin is a transmembrane protein that transports iron from the inside of a cell to the outside of it. It is found on the surface of cells that store or transport iron, including:

Recent research suggests that ferroportin is the key molecule regulated by hepcidin, the apparent "master regulator" of human iron metabolism.

Clinical significance

Ferroportin can be associated with African iron overload.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000138449Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025993Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

Further reading

External links