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{{Infobox_gene}}
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'''Glucose-6-phosphate translocase''' is an [[enzyme]] that in humans is encoded by the ''SLC37A4'' [[gene]].<ref name="pmid9428641">{{cite journal | vauthors = Gerin I, Veiga-da-Cunha M, Achouri Y, Collet JF, Van Schaftingen E | title = Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib | journal = FEBS Lett | volume = 419 | issue = 2–3 | pages = 235–8 |date=Jan 1998 | pmid = 9428641 | pmc =  | doi =10.1016/S0014-5793(97)01463-4 }}</ref><ref name="pmid9463334">{{cite journal | vauthors = Annabi B, Hiraiwa H, Mansfield BC, Lei KJ, Ubagai T, Polymeropoulos MH, Moses SW, Parvari R, Hershkovitz E, Mandel H, Fryman M, Chou JY | title = The gene for glycogen-storage disease type 1b maps to chromosome 11q23 | journal = Am J Hum Genet | volume = 62 | issue = 2 | pages = 400–5 |date=Apr 1998 | pmid = 9463334 | pmc = 1376902 | doi = 10.1086/301727 }}</ref><ref>{{cite web | title = Entrez Gene: SLC37A4 Solute carrier family 37 (glycerol-6-phosphate transporter), member 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2542| accessdate = }}</ref>
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{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Solute carrier family 37 (glycerol-6-phosphate transporter), member 4
| HGNCid = 4061
| Symbol = SLC37A4
| AltSymbols =; G6PT1; G6PT2; G6PT3; GSD1b; GSD1c; GSD1d; MGC15729; PRO0685; TRG19
| OMIM = 602671
| ECnumber =
| Homologene = 37482
| MGIid = 1316650
  | GeneAtlas_image1 = PBB_GE_SLC37A4_217289_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_SLC37A4_202830_s_at_tn.png
  | Function = {{GNF_GO|id=GO:0005215 |text = transporter activity}} {{GNF_GO|id=GO:0005351 |text = sugar:hydrogen ion symporter activity}}
| Component = {{GNF_GO|id=GO:0005783 |text = endoplasmic reticulum}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}}
| Process = {{GNF_GO|id=GO:0005977 |text = glycogen metabolic process}} {{GNF_GO|id=GO:0006006 |text = glucose metabolic process}} {{GNF_GO|id=GO:0006810 |text = transport}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 2542
    | Hs_Ensembl = ENSG00000137700
    | Hs_RefseqProtein = NP_001458
    | Hs_RefseqmRNA = NM_001467
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 11
    | Hs_GenLoc_start = 118400276
    | Hs_GenLoc_end = 118405289
    | Hs_Uniprot = O43826
    | Mm_EntrezGene = 14385
    | Mm_Ensembl = ENSMUSG00000032114
    | Mm_RefseqmRNA = NM_008063
    | Mm_RefseqProtein = NP_032089
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 9
    | Mm_GenLoc_start = 44149171
    | Mm_GenLoc_end = 44153963
    | Mm_Uniprot = 
  }}
}}
'''Solute carrier family 37 (glycerol-6-phosphate transporter), member 4''', also known as '''SLC37A4''', is a human [[gene]].<ref>{{cite web | title = Entrez Gene: SLC37A4 Solute carrier family 37 (glycerol-6-phosphate transporter), member 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2542| accessdate = }}</ref>


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| summary_text =  
}}
}}
==See also==
* [[Solute carrier family]]


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


==Further reading==
==Further reading==
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{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal  | author=Chou JY, Matern D, Mansfield BC, Chen YT |title=Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex. |journal=Curr. Mol. Med. |volume=2 |issue= 2 |pages= 121-43 |year= 2002 |pmid= 11949931 |doi=  }}
*{{cite journal  | vauthors=Chou JY, Matern D, Mansfield BC, Chen YT |title=Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex |journal=Curr. Mol. Med. |volume=2 |issue= 2 |pages= 121–43 |year= 2002 |pmid= 11949931 |doi=10.2174/1566524024605798 }}
*{{cite journal  | author=Narisawa K, Igarashi Y, Otomo H, Tada K |title=A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system. |journal=Biochem. Biophys. Res. Commun. |volume=83 |issue= 4 |pages= 1360-4 |year= 1978 |pmid= 212064 |doi=  }}
*{{cite journal  | vauthors=Narisawa K, Igarashi Y, Otomo H, Tada K |title=A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system |journal=Biochem. Biophys. Res. Commun. |volume=83 |issue= 4 |pages= 1360–4 |year= 1978 |pmid= 212064 |doi=10.1016/0006-291X(78)91371-2 }}
*{{cite journal | author=Gerin I, Veiga-da-Cunha M, Achouri Y, ''et al.'' |title=Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib. |journal=FEBS Lett. |volume=419 |issue= 2-3 |pages= 235-8 |year= 1998 |pmid= 9428641 |doi= }}
*{{cite journal   |vauthors=Fenske CD, Jeffery S, Weber JL, etal |title=Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q |journal=J. Med. Genet. |volume=35 |issue= 4 |pages= 269–72 |year= 1998 |pmid= 9598717 |doi=10.1136/jmg.35.4.269  | pmc=1051271  }}
*{{cite journal | author=Annabi B, Hiraiwa H, Mansfield BC, ''et al.'' |title=The gene for glycogen-storage disease type 1b maps to chromosome 11q23. |journal=Am. J. Hum. Genet. |volume=62 |issue= 2 |pages= 400-5 |year= 1998 |pmid= 9463334 |doi= }}
*{{cite journal   |vauthors=Kure S, Suzuki Y, Matsubara Y, etal |title=Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11 |journal=Biochem. Biophys. Res. Commun. |volume=248 |issue= 2 |pages= 426–31 |year= 1998 |pmid= 9675154 |doi= 10.1006/bbrc.1998.8985 }}
*{{cite journal | author=Fenske CD, Jeffery S, Weber JL, ''et al.'' |title=Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q. |journal=J. Med. Genet. |volume=35 |issue= 4 |pages= 269-72 |year= 1998 |pmid= 9598717 |doi=  }}
*{{cite journal   |vauthors=Veiga-da-Cunha M, Gerin I, Chen YT, etal |title=A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic |journal=Am. J. Hum. Genet. |volume=63 |issue= 4 |pages= 976–83 |year= 1998 |pmid= 9758626 |doi=10.1086/302068  | pmc=1377500 }}
*{{cite journal | author=Kure S, Suzuki Y, Matsubara Y, ''et al.'' |title=Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11. |journal=Biochem. Biophys. Res. Commun. |volume=248 |issue= 2 |pages= 426-31 |year= 1998 |pmid= 9675154 |doi= 10.1006/bbrc.1998.8985 }}
*{{cite journal   |vauthors=Marcolongo P, Barone V, Priori G, etal |title=Structure and mutation analysis of the glycogen storage disease type 1b gene |journal=FEBS Lett. |volume=436 |issue= 2 |pages= 247–50 |year= 1998 |pmid= 9781688 |doi=10.1016/S0014-5793(98)01129-6  }}
*{{cite journal | author=Veiga-da-Cunha M, Gerin I, Chen YT, ''et al.'' |title=A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic. |journal=Am. J. Hum. Genet. |volume=63 |issue= 4 |pages= 976-83 |year= 1998 |pmid= 9758626 |doi= }}
*{{cite journal   |vauthors=Lin B, Annabi B, Hiraiwa H, etal |title=Cloning and characterization of cDNAs encoding a candidate glycogen storage disease type 1b protein in rodents |journal=J. Biol. Chem. |volume=273 |issue= 48 |pages= 31656–60 |year= 1998 |pmid= 9822626 |doi=10.1074/jbc.273.48.31656  }}
*{{cite journal  | author=Marcolongo P, Barone V, Priori G, ''et al.'' |title=Structure and mutation analysis of the glycogen storage disease type 1b gene. |journal=FEBS Lett. |volume=436 |issue= 2 |pages= 247-50 |year= 1998 |pmid= 9781688 |doi=  }}
*{{cite journal  | vauthors=Ihara K, Kuromaru R, Hara T |title=Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib |journal=Hum. Genet. |volume=103 |issue= 4 |pages= 493–6 |year= 1998 |pmid= 9856496 |doi=10.1007/s004390050856 }}
*{{cite journal  | author=Lin B, Annabi B, Hiraiwa H, ''et al.'' |title=Cloning and characterization of cDNAs encoding a candidate glycogen storage disease type 1b protein in rodents. |journal=J. Biol. Chem. |volume=273 |issue= 48 |pages= 31656-60 |year= 1998 |pmid= 9822626 |doi=  }}
*{{cite journal  | vauthors=Ihara K, Takabayashi A, Terasaki K, Hara T |title=Assignment1 of glucose 6-phosphate translocase (G6PT1) to human chromosome band 11q23.3 by in situ hybridization |journal=Cytogenet. Cell Genet. |volume=83 |issue= 1–2 |pages= 50–1 |year= 1999 |pmid= 9925924 |doi=10.1159/000015167 }}
*{{cite journal  | author=Ihara K, Kuromaru R, Hara T |title=Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib. |journal=Hum. Genet. |volume=103 |issue= 4 |pages= 493-6 |year= 1998 |pmid= 9856496 |doi=  }}
*{{cite journal  | vauthors=Gerin I, Veiga-da-Cunha M, Noël G, Van Schaftingen E |title=Structure of the gene mutated in glycogen storage disease type Ib |journal=Gene |volume=227 |issue= 2 |pages= 189–95 |year= 1999 |pmid= 10023055 |doi=10.1016/S0378-1119(98)00614-3 }}
*{{cite journal | author=Ihara K, Takabayashi A, Terasaki K, Hara T |title=Assignment1 of glucose 6-phosphate translocase (G6PT1) to human chromosome band 11q23.3 by in situ hybridization. |journal=Cytogenet. Cell Genet. |volume=83 |issue= 1-2 |pages= 50-1 |year= 1999 |pmid= 9925924 |doi=  }}
*{{cite journal   |vauthors=Hiraiwa H, Pan CJ, Lin B, etal |title=Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b |journal=J. Biol. Chem. |volume=274 |issue= 9 |pages= 5532–6 |year= 1999 |pmid= 10026167 |doi=10.1074/jbc.274.9.5532 }}
*{{cite journal  | author=Gerin I, Veiga-da-Cunha M, Noël G, Van Schaftingen E |title=Structure of the gene mutated in glycogen storage disease type Ib. |journal=Gene |volume=227 |issue= 2 |pages= 189-95 |year= 1999 |pmid= 10023055 |doi=  }}
*{{cite journal  | vauthors=Pan CJ, Lin B, Chou JY |title=Transmembrane topology of human glucose 6-phosphate transporter |journal=J. Biol. Chem. |volume=274 |issue= 20 |pages= 13865–9 |year= 1999 |pmid= 10318794 |doi=10.1074/jbc.274.20.13865 }}
*{{cite journal | author=Hiraiwa H, Pan CJ, Lin B, ''et al.'' |title=Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b. |journal=J. Biol. Chem. |volume=274 |issue= 9 |pages= 5532-6 |year= 1999 |pmid= 10026167 |doi=  }}
*{{cite journal   |vauthors=Janecke AR, Bosshard NU, Mayatepek E, etal |title=Molecular diagnosis of type 1c glycogen storage disease |journal=Hum. Genet. |volume=104 |issue= 3 |pages= 275–7 |year= 1999 |pmid= 10323254 |doi=10.1007/s004390050948 }}
*{{cite journal | author=Pan CJ, Lin B, Chou JY |title=Transmembrane topology of human glucose 6-phosphate transporter. |journal=J. Biol. Chem. |volume=274 |issue= 20 |pages= 13865-9 |year= 1999 |pmid= 10318794 |doi=  }}
*{{cite journal   |vauthors=Hou DC, Kure S, Suzuki Y, etal |title=Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene |journal=Am. J. Med. Genet. |volume=86 |issue= 3 |pages= 253–7 |year= 1999 |pmid= 10482875 |doi=10.1002/(SICI)1096-8628(19990917)86:3<253::AID-AJMG11>3.0.CO;2-7 }}
*{{cite journal  | author=Janecke AR, Bosshard NU, Mayatepek E, ''et al.'' |title=Molecular diagnosis of type 1c glycogen storage disease. |journal=Hum. Genet. |volume=104 |issue= 3 |pages= 275-7 |year= 1999 |pmid= 10323254 |doi= }}
*{{cite journal  |vauthors=Veiga-da-Cunha M, Gerin I, Chen YT, etal |title=The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a |journal=Eur. J. Hum. Genet. |volume=7 |issue= 6 |pages= 717–23 |year= 1999 |pmid= 10482962 |doi= 10.1038/sj.ejhg.5200366 }}
*{{cite journal | author=Hou DC, Kure S, Suzuki Y, ''et al.'' |title=Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene. |journal=Am. J. Med. Genet. |volume=86 |issue= 3 |pages= 253-7 |year= 1999 |pmid= 10482875 |doi= }}
*{{cite journal   |vauthors=Galli L, Orrico A, Marcolongo P, etal |title=Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c |journal=FEBS Lett. |volume=459 |issue= 2 |pages= 255–8 |year= 1999 |pmid= 10518030 |doi=10.1016/S0014-5793(99)01248-X }}
*{{cite journal  | author=Veiga-da-Cunha M, Gerin I, Chen YT, ''et al.'' |title=The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a. |journal=Eur. J. Hum. Genet. |volume=7 |issue= 6 |pages= 717-23 |year= 1999 |pmid= 10482962 |doi= 10.1038/sj.ejhg.5200366 }}
*{{cite journal   |vauthors=Lam CW, Chan KY, Tong SF, etal |title=A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b |journal=Hum. Mutat. |volume=16 |issue= 1 |pages= 94 |year= 2000 |pmid= 10874322 |doi= 10.1002/1098-1004(200007)16:1<94::AID-HUMU26>3.0.CO;2-Q }}
*{{cite journal  | author=Galli L, Orrico A, Marcolongo P, ''et al.'' |title=Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c. |journal=FEBS Lett. |volume=459 |issue= 2 |pages= 255-8 |year= 1999 |pmid= 10518030 |doi= }}
*{{cite journal   |vauthors=Santer R, Rischewski J, Block G, etal |title=Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients |journal=Hum. Mutat. |volume=16 |issue= 2 |pages= 177 |year= 2000 |pmid= 10923042 |doi= 10.1002/1098-1004(200008)16:2<177::AID-HUMU13>3.0.CO;2-8 }}
*{{cite journal | author=Lam CW, Chan KY, Tong SF, ''et al.'' |title=A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b. |journal=Hum. Mutat. |volume=16 |issue= 1 |pages= 94 |year= 2000 |pmid= 10874322 |doi= 10.1002/1098-1004(200007)16:1<94::AID-HUMU26>3.0.CO;2-Q }}
*{{cite journal | author=Santer R, Rischewski J, Block G, ''et al.'' |title=Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients. |journal=Hum. Mutat. |volume=16 |issue= 2 |pages= 177 |year= 2000 |pmid= 10923042 |doi= 10.1002/1098-1004(200008)16:2<177::AID-HUMU13>3.0.CO;2-8 }}
}}
}}
{{refend}}
{{refend}}


{{Membrane transport proteins}}
{{Membrane transport proteins}}
[[Category:Membrane biology]]
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[[Category:Integral membrane proteins]]
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[[Category:Solute carrier family]]
 
 
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Latest revision as of 06:32, 11 September 2017

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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

Glucose-6-phosphate translocase is an enzyme that in humans is encoded by the SLC37A4 gene.[1][2][3]


See also

References

  1. ↑ Gerin I, Veiga-da-Cunha M, Achouri Y, Collet JF, Van Schaftingen E (Jan 1998). "Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib". FEBS Lett. 419 (2–3): 235–8. doi:10.1016/S0014-5793(97)01463-4. PMID 9428641.
  2. ↑ Annabi B, Hiraiwa H, Mansfield BC, Lei KJ, Ubagai T, Polymeropoulos MH, Moses SW, Parvari R, Hershkovitz E, Mandel H, Fryman M, Chou JY (Apr 1998). "The gene for glycogen-storage disease type 1b maps to chromosome 11q23". Am J Hum Genet. 62 (2): 400–5. doi:10.1086/301727. PMC 1376902. PMID 9463334.
  3. ↑ "Entrez Gene: SLC37A4 Solute carrier family 37 (glycerol-6-phosphate transporter), member 4".

Further reading


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