| 释义 |
- See also
- References
- Further reading
{{Infobox_gene}}Glucose-6-phosphate translocase is an enzyme that in humans is encoded by the SLC37A4 gene.[1][2][3]See alsoReferences1. ^{{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 }}
2. ^{{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 }}
3. ^{{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 = }}
Further reading{{refbegin | 2}}- {{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 | 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 |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 |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 |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 |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 |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 | 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 | 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 | 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 |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 | 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 |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 |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 |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 |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 |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 |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 }}
{{refend}}{{Membrane transport proteins}}{{membrane-protein-stub}} 1 : Solute carrier family |