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SLC35C1 - Revision history
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WikiBot: Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +)
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<p>Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +)</p>
<p><b>New page</b></p><div><!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. --><br />
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. --><br />
{{GNF_Protein_box<br />
| image = <br />
| image_source = <br />
| PDB = <br />
| Name = Solute carrier family 35, member C1<br />
| HGNCid = 20197<br />
| Symbol = SLC35C1<br />
| AltSymbols =; FLJ11320; FLJ14841; FUCT1<br />
| OMIM = 605881<br />
| ECnumber = <br />
| Homologene = 41258<br />
| MGIid = 2443301<br />
| GeneAtlas_image1 = PBB_GE_SLC35C1_218485_s_at_tn.png<br />
| Function = {{GNF_GO|id=GO:0005351 |text = sugar:hydrogen ion symporter activity}} <br />
| Component = {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}} <br />
| Process = {{GNF_GO|id=GO:0006810 |text = transport}} <br />
| Orthologs = {{GNF_Ortholog_box<br />
| Hs_EntrezGene = 55343<br />
| Hs_Ensembl = ENSG00000181830<br />
| Hs_RefseqProtein = NP_060859<br />
| Hs_RefseqmRNA = NM_018389<br />
| Hs_GenLoc_db = <br />
| Hs_GenLoc_chr = 11<br />
| Hs_GenLoc_start = 45783217<br />
| Hs_GenLoc_end = 45791142<br />
| Hs_Uniprot = Q96A29<br />
| Mm_EntrezGene = 228368<br />
| Mm_Ensembl = ENSMUSG00000049922<br />
| Mm_RefseqmRNA = NM_145832<br />
| Mm_RefseqProtein = NP_665831<br />
| Mm_GenLoc_db = <br />
| Mm_GenLoc_chr = 2<br />
| Mm_GenLoc_start = 92253594<br />
| Mm_GenLoc_end = 92261357<br />
| Mm_Uniprot = <br />
}}<br />
}}<br />
'''Solute carrier family 35, member C1''', also known as '''SLC35C1''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SLC35C1 solute carrier family 35, member C1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55343| accessdate = }}</ref><br />
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==See also==<br />
* [[Solute carrier family]]<br />
<br />
==References==<br />
{{reflist|2}}<br />
<br />
==Further reading==<br />
{{refbegin | 2}}<br />
{{PBB_Further_reading <br />
| citations = <br />
*{{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= }}<br />
*{{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= }}<br />
*{{cite journal | author=Lühn K, Wild MK, Eckhardt M, ''et al.'' |title=The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter. |journal=Nat. Genet. |volume=28 |issue= 1 |pages= 69-72 |year= 2001 |pmid= 11326279 |doi= 10.1038/88289 }}<br />
*{{cite journal | author=Lübke T, Marquardt T, Etzioni A, ''et al.'' |title=Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency. |journal=Nat. Genet. |volume=28 |issue= 1 |pages= 73-6 |year= 2001 |pmid= 11326280 |doi= 10.1038/88299 }}<br />
*{{cite journal | author=Hidalgo A, Ma S, Peired AJ, ''et al.'' |title=Insights into leukocyte adhesion deficiency type 2 from a novel mutation in the GDP-fucose transporter gene. |journal=Blood |volume=101 |issue= 5 |pages= 1705-12 |year= 2003 |pmid= 12406889 |doi= 10.1182/blood-2002-09-2840 }}<br />
*{{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 }}<br />
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}<br />
*{{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 }}<br />
*{{cite journal | author=Helmus Y, Denecke J, Yakubenia S, ''et al.'' |title=Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter. |journal=Blood |volume=107 |issue= 10 |pages= 3959-66 |year= 2006 |pmid= 16455955 |doi= 10.1182/blood-2005-08-3334 }}<br />
}}<br />
{{refend}}<br />
<br />
{{membrane-protein-stub}}<br />
{{NLM content}}<br />
{{Membrane transport proteins}}<br />
[[Category:Solute carrier family]]<br />
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