View source for GPATCH8

{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
'''G patch domain-containing protein 8''' is a [[protein]] that in humans is encoded by the ''GPATCH8'' [[gene]].<ref name="pmid9628581">{{cite journal |vauthors=Nagase T, Ishikawa K, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O | title = Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro | journal = DNA Res | volume = 5 | issue = 1 | pages = 31–9 | date = Aug 1998 | pmid = 9628581 | doi = 10.1093/dnares/5.1.31 | doi-access = free }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: GPATCH8 G patch domain containing 8| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23131}}</ref>
==Hyperuricemia==
[[Hyperuricemia]] cosegregating with [[osteogenesis imperfecta]] has been shown to be associated with a mutation in '''GPATCH8''' using [[exome sequencing]]<ref>{{cite journal |vauthors=Kaneko H, Kitoh H, Matsuura T, Masuda A, Ito M, Mottes M, Rauch F, Ishiguro N, Ohno K | title = Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in '''GPATCH8''' | journal = Hum. Genet. | volume = 130 | issue = 5 | pages = 671–83 | date = Nov 2011 | pmid = 21594610 | doi = 10.1007/s00439-011-1006-9 | s2cid = 1075364 }}</ref>
==References==
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==Further reading==
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*{{cite journal |vauthors=Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–48 | year = 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 | s2cid = 7827573 | doi-access = free }}
*{{cite journal|author-link13=Huda Zoghbi |vauthors=Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY | title = A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration | journal = Cell | volume = 125 | issue = 4 | pages = 801–14 | year = 2006 | pmid = 16713569 | doi = 10.1016/j.cell.2006.03.032 |s2cid=13709685 | doi-access = free }}
*{{cite journal |vauthors=Nousiainen M, Silljé HH, Sauer G, Nigg EA, Körner R | title = Phosphoproteome analysis of the human mitotic spindle | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 103 | issue = 14 | pages = 5391–6 | year = 2006 | pmid = 16565220 | pmc = 1459365 | doi = 10.1073/pnas.0507066103 | bibcode = 2006PNAS..103.5391N | doi-access = free }}
*{{cite journal |vauthors=McKinney JL, Murdoch DJ, Wang J, Robinson J, Biltcliffe C, Khan HM, Walker PM, Savage J, Skerjanc I, Hegele RA | title = Venn analysis as part of a bioinformatic approach to prioritize expressed sequence tags from cardiac libraries | journal = Clin. Biochem. | volume = 37 | issue = 11 | pages = 953–60 | year = 2005 | pmid = 15498521 | doi = 10.1016/j.clinbiochem.2004.07.010 }}
*{{cite journal |vauthors=Beausoleil SA, Jedrychowski M, Schwartz D, Elias JE, Villén J, Li J, Cohn MA, Cantley LC, Gygi SP | title = Large-scale characterization of HeLa cell nuclear phosphoproteins | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 101 | issue = 33 | pages = 12130–5 | year = 2004 | pmid = 15302935 | pmc = 514446 | doi = 10.1073/pnas.0404720101 | bibcode = 2004PNAS..10112130B | doi-access = free }}
*{{cite journal |vauthors=Thornton MA, Poncz M, Korostishevsky M, Yakobson E, Usher S, Seligsohn U, Peretz H | title = The human platelet alphaIIb gene is not closely linked to its integrin partner beta3 | journal = Blood | volume = 94 | issue = 6 | pages = 2039–47 | year = 1999 | pmid = 10477733 | doi =  10.1182/blood.V94.6.2039}}
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{{gene-17-stub}}