Glypican 4: Difference between revisions

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'''Glypican-4''' is a [[protein]] that in humans is encoded by the ''GPC4'' [[gene]].<ref name="pmid9787072">{{cite journal |vauthors=Veugelers M, Vermeesch J, Watanabe K, Yamaguchi Y, Marynen P, David G | title = GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome | journal = Genomics | volume = 53 | issue = 1 | pages = 1–11 |date=Dec 1998 | pmid = 9787072 | pmc =  | doi = 10.1006/geno.1998.5465 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: GPC4 glypican 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2239| accessdate = }}</ref>
'''Glypican-4''' is a [[protein]] that in humans is encoded by the ''GPC4'' [[gene]].<ref name="pmid9787072">{{cite journal |vauthors=Veugelers M, Vermeesch J, Watanabe K, Yamaguchi Y, Marynen P, David G | title = GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome | journal = Genomics | volume = 53 | issue = 1 | pages = 1–11 |date=Dec 1998 | pmid = 9787072 | pmc =  | doi = 10.1006/geno.1998.5465 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: GPC4 glypican 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2239| accessdate = }}</ref>
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{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal  |vauthors=Ross MT, Grafham DV, Coffey AJ, etal |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440  | pmc=2665286 }}
*{{cite journal  |vauthors=Ross MT, Grafham DV, Coffey AJ, etal |title=The DNA sequence of the human X chromosome |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440  | pmc=2665286 }}
*{{cite journal  |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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  | pmc=528928 }}
*{{cite journal  |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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  | pmc=528928 }}
*{{cite journal  |vauthors=Clark HF, Gurney AL, Abaya E, etal |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003  | pmc=403697 }}
*{{cite journal  |vauthors=Clark HF, Gurney AL, Abaya E, etal |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003  | pmc=403697 }}
*{{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 }}
*{{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 }}
*{{cite journal  |vauthors=Sheu TJ, Schwarz EM, O'Keefe RJ, etal |title=Use of a phage display technique to identify potential osteoblast binding sites within osteoclast lacunae. |journal=J. Bone Miner. Res. |volume=17 |issue= 5 |pages= 915–22 |year= 2002 |pmid= 12009023 |doi=10.1359/jbmr.2002.17.5.915  }}
*{{cite journal  |vauthors=Sheu TJ, Schwarz EM, O'Keefe RJ, etal |title=Use of a phage display technique to identify potential osteoblast binding sites within osteoclast lacunae |journal=J. Bone Miner. Res. |volume=17 |issue= 5 |pages= 915–22 |year= 2002 |pmid= 12009023 |doi=10.1359/jbmr.2002.17.5.915  }}
*{{cite journal  |vauthors=Karumanchi SA, Jha V, Ramchandran R, etal |title=Cell surface glypicans are low-affinity endostatin receptors. |journal=Mol. Cell |volume=7 |issue= 4 |pages= 811–22 |year= 2001 |pmid= 11336704 |doi=10.1016/S1097-2765(01)00225-8  }}
*{{cite journal  |vauthors=Karumanchi SA, Jha V, Ramchandran R, etal |title=Cell surface glypicans are low-affinity endostatin receptors |journal=Mol. Cell |volume=7 |issue= 4 |pages= 811–22 |year= 2001 |pmid= 11336704 |doi=10.1016/S1097-2765(01)00225-8  }}
*{{cite journal  |vauthors=Hagihara K, Watanabe K, Chun J, Yamaguchi Y |title=Glypican-4 is an FGF2-binding heparan sulfate proteoglycan expressed in neural precursor cells. |journal=Dev. Dyn. |volume=219 |issue= 3 |pages= 353–67 |year= 2000 |pmid= 11066092 |doi= 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1059>3.0.CO;2-# }}
*{{cite journal  |vauthors=Hagihara K, Watanabe K, Chun J, Yamaguchi Y |title=Glypican-4 is an FGF2-binding heparan sulfate proteoglycan expressed in neural precursor cells |journal=Dev. Dyn. |volume=219 |issue= 3 |pages= 353–67 |year= 2000 |pmid= 11066092 |doi= 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1059>3.0.CO;2-# |doi-broken-date=2018-09-06 }}
*{{cite journal  |vauthors=Veugelers M, Cat BD, Muyldermans SY, etal |title=Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene. |journal=Hum. Mol. Genet. |volume=9 |issue= 9 |pages= 1321–8 |year= 2000 |pmid= 10814714 |doi=10.1093/hmg/9.9.1321  }}
*{{cite journal  |vauthors=Veugelers M, Cat BD, Muyldermans SY, etal |title=Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene |journal=Hum. Mol. Genet. |volume=9 |issue= 9 |pages= 1321–8 |year= 2000 |pmid= 10814714 |doi=10.1093/hmg/9.9.1321  }}
*{{cite journal  |vauthors=Siebertz B, Stöcker G, Drzeniek Z, etal |title=Expression of glypican-4 in haematopoietic-progenitor and bone-marrow-stromal cells. | series=344 |journal=Biochem. J. |volume=Pt 3 |issue=  |pages= 937–43 |year= 2000 |pmid= 10585884 |doi=  | pmc=1220719  }}
*{{cite journal  |vauthors=Siebertz B, Stöcker G, Drzeniek Z, etal |title=Expression of glypican-4 in haematopoietic-progenitor and bone-marrow-stromal cells  | series=344 |journal=Biochem. J. |volume=Pt 3 |issue=  |pages= 937–43 |year= 2000 |pmid= 10585884 |doi=  | pmc=1220719  }}
*{{cite journal  |vauthors=Huber R, Mazzarella R, Chen CN, etal |title=Glypican 3 and glypican 4 are juxtaposed in Xq26.1. |journal=Gene |volume=225 |issue= 1-2 |pages= 9–16 |year= 1999 |pmid= 9931407 |doi=10.1016/S0378-1119(98)00549-6  }}
*{{cite journal  |vauthors=Huber R, Mazzarella R, Chen CN, etal |title=Glypican 3 and glypican 4 are juxtaposed in Xq26.1 |journal=Gene |volume=225 |issue= 1–2 |pages= 9–16 |year= 1999 |pmid= 9931407 |doi=10.1016/S0378-1119(98)00549-6  |url=https://zenodo.org/record/1260055 }}
*{{cite journal  |vauthors=Watanabe K, Yamada H, Yamaguchi Y |title=K-glypican: a novel GPI-anchored heparan sulfate proteoglycan that is highly expressed in developing brain and kidney. |journal=J. Cell Biol. |volume=130 |issue= 5 |pages= 1207–18 |year= 1995 |pmid= 7657705 |doi=10.1083/jcb.130.5.1207  | pmc=2120559  }}
*{{cite journal  |vauthors=Watanabe K, Yamada H, Yamaguchi Y |title=K-glypican: a novel GPI-anchored heparan sulfate proteoglycan that is highly expressed in developing brain and kidney |journal=J. Cell Biol. |volume=130 |issue= 5 |pages= 1207–18 |year= 1995 |pmid= 7657705 |doi=10.1083/jcb.130.5.1207  | pmc=2120559  }}
}}
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Latest revision as of 05:36, 12 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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

Glypican-4 is a protein that in humans is encoded by the GPC4 gene.[1][2]

Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The GPC4 gene is adjacent to the 3' end of GPC3 and may also play a role in Simpson-Golabi-Behmel syndrome.[2]

See also

References

  1. Veugelers M, Vermeesch J, Watanabe K, Yamaguchi Y, Marynen P, David G (Dec 1998). "GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome". Genomics. 53 (1): 1–11. doi:10.1006/geno.1998.5465. PMID 9787072.
  2. 2.0 2.1 "Entrez Gene: GPC4 glypican 4".

Further reading

External links