SLC31A2: Difference between revisions

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{{Infobox_gene}}
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'''Probable low affinity copper uptake protein 2''' is a [[protein]] that in humans is encoded by the ''SLC31A2'' [[gene]].<ref name="pmid9207117">{{cite journal | vauthors = Zhou B, Gitschier J | title = hCTR1: a human gene for copper uptake identified by complementation in yeast | journal = Proc Natl Acad Sci U S A | volume = 94 | issue = 14 | pages = 7481–6 | date = Aug 1997 | pmid = 9207117 | pmc = 23847 | doi = 10.1073/pnas.94.14.7481 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1318| accessdate = }}</ref>
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== See also ==
{{GNF_Protein_box
| image = 
| image_source = 
| PDB =
| Name = Solute carrier family 31 (copper transporters), member 2
| HGNCid = 11017
| Symbol = SLC31A2
| AltSymbols =; COPT2; CTR2; hCTR2
| OMIM = 603088
| ECnumber = 
| Homologene = 37536
| MGIid = 1333844
| GeneAtlas_image1 = PBB_GE_SLC31A2_204204_at_tn.png
| Function = {{GNF_GO|id=GO:0005375 |text = copper ion transmembrane transporter activity}} {{GNF_GO|id=GO:0005507 |text = copper ion binding}}
| Component = {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0006811 |text = ion transport}} {{GNF_GO|id=GO:0006825 |text = copper ion transport}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 1318
    | Hs_Ensembl = ENSG00000136867
    | Hs_RefseqProtein = NP_001851
    | Hs_RefseqmRNA = NM_001860
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 9
    | Hs_GenLoc_start = 114953108
    | Hs_GenLoc_end = 114966241
    | Hs_Uniprot = O15432
    | Mm_EntrezGene = 20530
    | Mm_Ensembl = ENSMUSG00000066152
    | Mm_RefseqmRNA = XM_981201
    | Mm_RefseqProtein = XP_986295
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 4
    | Mm_GenLoc_start = 61772806
    | Mm_GenLoc_end = 61784772
    | Mm_Uniprot = Q3U9W6
  }}
}}
'''Solute carrier family 31 (copper transporters), member 2''', also known as '''SLC31A2''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1318| accessdate = }}</ref>
 
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{{PBB_Summary
| section_title =
| summary_text =
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==See also==
* [[Solute carrier family]]
* [[Solute carrier family]]


==References==
== References ==
{{reflist|2}}
{{reflist}}


==Further reading==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Suzuki Y, Yamashita R, Shirota M, Sakakibara Y, Chiba J, Mizushima-Sugano J, Nakai K, Sugano S | title = Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions | journal = Genome Res. | volume = 14 | issue = 9 | pages = 1711–8 | year = 2004 | pmid = 15342556 | pmc = 515316 | doi = 10.1101/gr.2435604 }}
| citations =
* {{cite journal | vauthors = van den Berghe PV, Folmer DE, Malingré HE, van Beurden E, Klomp AE, van de Sluis B, Merkx M, Berger R, Klomp LW | title = Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake | journal = Biochem. J. | volume = 407 | issue = 1 | pages = 49–59 | year = 2007 | pmid = 17617060 | pmc = 2267400 | doi = 10.1042/BJ20070705 }}
*{{cite journal  | author=Zhou B, Gitschier J |title=hCTR1: a human gene for copper uptake identified by complementation in yeast. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=94 |issue= 14 |pages= 7481-6 |year= 1997 |pmid= 9207117 |doi=  }}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal | author=Suzuki Y, Yamashita R, Shirota M, ''et al.'' |title=Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions. |journal=Genome Res. |volume=14 |issue= 9 |pages= 1711-8 |year= 2004 |pmid= 15342556 |doi= 10.1101/gr.2435604 }}
*{{cite journal  | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal | author=van den Berghe PV, Folmer DE, Malingré HE, ''et al.'' |title=Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake. |journal=Biochem. J. |volume=407 |issue= 1 |pages= 49-59 |year= 2007 |pmid= 17617060 |doi= 10.1042/BJ20070705 }}
}}
{{refend}}
{{refend}}


{{membrane-protein-stub}}
{{Membrane transport proteins}}
{{Membrane transport proteins}}
[[Category:Solute carrier family]]
[[Category:Solute carrier family]]
{{WikiDoc Sources}}
 
 
{{membrane-protein-stub}}

Latest revision as of 01:11, 27 October 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.[1][2]

See also

References

  1. Zhou B, Gitschier J (Aug 1997). "hCTR1: a human gene for copper uptake identified by complementation in yeast". Proc Natl Acad Sci U S A. 94 (14): 7481–6. doi:10.1073/pnas.94.14.7481. PMC 23847. PMID 9207117.
  2. "Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2".

Further reading