SLC15A2: Difference between revisions

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Importing Wikidata short description: Protein-coding gene in the species Homo sapiens (shortdescs-in-category)
 
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{{Short description|Protein-coding gene in the species Homo sapiens}}
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{{Infobox_gene}}
{{PBB_Controls
'''Solute carrier family 15 (H+/peptide transporter), member 2''', also known as '''SLC15A2''', is a [[human]] [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SLC15A2 solute carrier family 15 (H+/peptide transporter), member 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6565}}</ref>
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==See also==
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* [[Solute carrier family]]
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Solute carrier family 15 (H+/peptide transporter), member 2
| HGNCid = 10921
| Symbol = SLC15A2
| AltSymbols =; PEPT2
| OMIM = 602339
| ECnumber =
| Homologene = 56912
| MGIid = 1890457
| GeneAtlas_image1 = PBB_GE_SLC15A2_205317_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_SLC15A2_205316_at_tn.png
| Function = {{GNF_GO|id=GO:0005215 |text = transporter activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0015198 |text = oligopeptide transporter activity}} {{GNF_GO|id=GO:0015293 |text = symporter activity}} {{GNF_GO|id=GO:0015333 |text = peptide:hydrogen symporter activity}} {{GNF_GO|id=GO:0015334 |text = high affinity oligopeptide transporter activity}}
| Component = {{GNF_GO|id=GO:0005624 |text = membrane fraction}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0006857 |text = oligopeptide transport}} {{GNF_GO|id=GO:0015031 |text = protein transport}} {{GNF_GO|id=GO:0015893 |text = drug transport}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 6565
| Hs_Ensembl = ENSG00000163406
| Hs_RefseqProtein = NP_066568
| Hs_RefseqmRNA = NM_021082
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 3
| Hs_GenLoc_start = 123095977
| Hs_GenLoc_end = 123143147
| Hs_Uniprot = Q16348
| Mm_EntrezGene = 57738
| Mm_Ensembl = ENSMUSG00000022899
| Mm_RefseqmRNA = NM_021301
| Mm_RefseqProtein = NP_067276
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 16
| Mm_GenLoc_start = 36669420
| Mm_GenLoc_end = 36704201
| Mm_Uniprot = Q80XC0
}}
}}
'''Solute carrier family 15 (H+/peptide transporter), member 2''', also known as '''SLC15A2''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SLC15A2 solute carrier family 15 (H+/peptide transporter), member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6565| accessdate = }}</ref>

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{{PBB_Summary
| section_title =
| summary_text =
}}


==References==
==References==
{{reflist}}
{{reflist}}

==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
*{{cite journal |vauthors=Liu W, Liang R, Ramamoorthy S, etal |title=Molecular cloning of PEPT 2, a new member of the H+/peptide cotransporter family, from human kidney. |journal=Biochim. Biophys. Acta |volume=1235 |issue= 2 |pages= 461–6 |year= 1995 |pmid= 7756356 |doi=10.1016/0005-2736(95)80036-F |doi-access=free }}
{{PBB_Further_reading
*{{cite journal | vauthors=Döring F, Martini C, Walter J, Daniel H |title=Importance of a small N-terminal region in mammalian peptide transporters for substrate affinity and function. |journal=J. Membr. Biol. |volume=186 |issue= 2 |pages= 55–62 |year= 2002 |pmid= 11944083 |doi= 10.1007/s00232-001-0135-9 |s2cid=11211548 }}
| citations =
*{{cite journal | author=Liu W, Liang R, Ramamoorthy S, ''et al.'' |title=Molecular cloning of PEPT 2, a new member of the H+/peptide cotransporter family, from human kidney. |journal=Biochim. Biophys. Acta |volume=1235 |issue= 2 |pages= 461-6 |year= 1995 |pmid= 7756356 |doi= }}
*{{cite journal | vauthors=Alcorn J, Lu X, Moscow JA, McNamara PJ |title=Transporter gene expression in lactating and nonlactating human mammary epithelial cells using real-time reverse transcription-polymerase chain reaction. |journal=J. Pharmacol. Exp. Ther. |volume=303 |issue= 2 |pages= 487–96 |year= 2002 |pmid= 12388627 |doi= 10.1124/jpet.102.038315 |s2cid=16195525 }}
*{{cite journal | author=Döring F, Martini C, Walter J, Daniel H |title=Importance of a small N-terminal region in mammalian peptide transporters for substrate affinity and function. |journal=J. Membr. Biol. |volume=186 |issue= 2 |pages= 55-62 |year= 2002 |pmid= 11944083 |doi= 10.1007/s00232-001-0135-9 }}
*{{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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 | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
*{{cite journal | author=Alcorn J, Lu X, Moscow JA, McNamara PJ |title=Transporter gene expression in lactating and nonlactating human mammary epithelial cells using real-time reverse transcription-polymerase chain reaction. |journal=J. Pharmacol. Exp. Ther. |volume=303 |issue= 2 |pages= 487-96 |year= 2002 |pmid= 12388627 |doi= 10.1124/jpet.102.038315 }}
*{{cite journal | author=Groneberg DA |title=[Expression, localization and functional aspects of the peptide transporter PEPT2 in the normal respiratory tract and in cystic fibrosis] |journal=Pneumologie (Stuttgart, Germany) |volume=57 |issue= 2 |pages= 104–5 |year= 2003 |pmid= 12579467 |doi= 10.1055/s-2003-37158 |doi-access= free }}
*{{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 | vauthors=Terada T, Irie M, Okuda M, Inui K |title=Genetic variant Arg57His in human H+/peptide cotransporter 2 causes a complete loss of transport function. |journal=Biochem. Biophys. Res. Commun. |volume=316 |issue= 2 |pages= 416–20 |year= 2004 |pmid= 15020234 |doi= 10.1016/j.bbrc.2004.02.063 }}
*{{cite journal | author=Groneberg DA |title=[Expression, localization and functional aspects of the peptide transporter PEPT2 in the normal respiratory tract and in cystic fibrosis] |journal=Pneumologie (Stuttgart, Germany) |volume=57 |issue= 2 |pages= 104-5 |year= 2003 |pmid= 12579467 |doi= 10.1055/s-2003-37158 }}
*{{cite journal | vauthors=Pinsonneault J, Nielsen CU, Sadée W |title=Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions. |journal=J. Pharmacol. Exp. Ther. |volume=311 |issue= 3 |pages= 1088–96 |year= 2005 |pmid= 15282265 |doi= 10.1124/jpet.104.073098 |s2cid=12947228 }}
*{{cite journal | author=Terada T, Irie M, Okuda M, Inui K |title=Genetic variant Arg57His in human H+/peptide cotransporter 2 causes a complete loss of transport function. |journal=Biochem. Biophys. Res. Commun. |volume=316 |issue= 2 |pages= 416-20 |year= 2004 |pmid= 15020234 |doi= 10.1016/j.bbrc.2004.02.063 }}
*{{cite journal |vauthors=Bahadduri PM, D'Souza VM, Pinsonneault JK, etal |title=Functional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epithelium. |journal=Am. J. Respir. Cell Mol. Biol. |volume=32 |issue= 4 |pages= 319–25 |year= 2005 |pmid= 15626774 |doi= 10.1165/rcmb.2004-0322OC }}
*{{cite journal | author=Pinsonneault J, Nielsen CU, Sadée W |title=Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions. |journal=J. Pharmacol. Exp. Ther. |volume=311 |issue= 3 |pages= 1088-96 |year= 2005 |pmid= 15282265 |doi= 10.1124/jpet.104.073098 }}
*{{cite journal |vauthors=Zhang EY, Emerick RM, Pak YA, etal |title=Comparison of human and monkey peptide transporters: PEPT1 and PEPT2. |journal=Mol. Pharm. |volume=1 |issue= 3 |pages= 201–10 |year= 2005 |pmid= 15981923 |doi=10.1021/mp0499712 }}
*{{cite journal | author=Bahadduri PM, D'Souza VM, Pinsonneault JK, ''et al.'' |title=Functional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epithelium. |journal=Am. J. Respir. Cell Mol. Biol. |volume=32 |issue= 4 |pages= 319-25 |year= 2005 |pmid= 15626774 |doi= 10.1165/rcmb.2004-0322OC }}
*{{cite journal |vauthors=Noshiro R, Anzai N, Sakata T, etal |title=The PDZ domain protein PDZK1 interacts with human peptide transporter PEPT2 and enhances its transport activity. |journal=Kidney Int. |volume=70 |issue= 2 |pages= 275–82 |year= 2006 |pmid= 16738539 |doi= 10.1038/sj.ki.5001522 |doi-access= free }}
*{{cite journal | author=Zhang EY, Emerick RM, Pak YA, ''et al.'' |title=Comparison of human and monkey peptide transporters: PEPT1 and PEPT2. |journal=Mol. Pharm. |volume=1 |issue= 3 |pages= 201-10 |year= 2005 |pmid= 15981923 |doi= }}
*{{cite journal |vauthors=Søndergaard H, Bravo S, Nielsen CU, etal |title=Cloning of the pig PEPT2 (pPEPT2) and characterization of the effects of epidermal growth factor (EGF) on pPEPT2-mediated peptide uptake in the renal porcine cell line LLC-PK1. |journal=Eur. J. Pharm. Sci. |volume=33 |issue= 4 |pages= 332–42 |year= 2008 |pmid= 18295462|doi= 10.1016/j.ejps.2008.01.001 |doi-access= free }}
*{{cite journal | author=Noshiro R, Anzai N, Sakata T, ''et al.'' |title=The PDZ domain protein PDZK1 interacts with human peptide transporter PEPT2 and enhances its transport activity. |journal=Kidney Int. |volume=70 |issue= 2 |pages= 275-82 |year= 2006 |pmid= 16738539 |doi= 10.1038/sj.ki.5001522 }}
}}
{{refend}}
{{refend}}


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

[[Category:Solute carrier family]]


{{membrane-protein-stub}}

Latest revision as of 22:22, 3 March 2023

SLC15A2
Identifiers
AliasesSLC15A2, PEPT2, solute carrier family 15 member 2
External IDsOMIM: 602339; MGI: 1890457; HomoloGene: 56912; GeneCards: SLC15A2; OMA:SLC15A2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145998
NM_021082

NM_001145899
NM_021301

RefSeq (protein)

NP_001139470
NP_066568

n/a

Location (UCSC)Chr 3: 121.89 – 121.94 MbChr 16: 36.57 – 36.61 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 15 (H+/peptide transporter), member 2, also known as SLC15A2, is a human gene.[5]

See also[edit]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163406Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022899Ensembl, 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.
  5. ^ "Entrez Gene: SLC15A2 solute carrier family 15 (H+/peptide transporter), member 2".

Further reading[edit]