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{{PBB|geneid=25894}}
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'''Puratrophin-1''' is a [[protein]] that in humans is encoded by the ''PLEKHG4'' [[gene]].<ref name="pmid16491300">{{cite journal | vauthors = Wieczorek S, Arning L, Alheite I, Epplen JT | title = Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population | journal = J Hum Genet | volume = 51 | issue = 4 | pages = 363–7 |date=Apr 2006 | pmid = 16491300 | pmc =  | doi = 10.1007/s10038-006-0372-y }}</ref><ref name="pmid16001362">{{cite journal | vauthors = Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H | title = An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains | journal = Am J Hum Genet | volume = 77 | issue = 2 | pages = 280–96 |date=Jul 2005 | pmid = 16001362 | pmc = 1224530 | doi = 10.1086/432518 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=25894| accessdate = }}</ref>
 
'''Pleckstrin homology domain containing, family G (with RhoGef domain) member 4''', also known as '''PLEKHG4''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=25894| accessdate = }}</ref>
 
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==References==
==References==
{{reflist}}
{{reflist}}
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal | author=Flanigan K, Gardner K, Alderson K, ''et al.'' |title=Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. |journal=Am. J. Hum. Genet. |volume=59 |issue= 2 |pages= 392–9 |year= 1996 |pmid= 8755926 |doi=  }}
*{{cite journal   |vauthors=Flanigan K, Gardner K, Alderson K, etal |title=Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. |journal=Am. J. Hum. Genet. |volume=59 |issue= 2 |pages= 392–9 |year= 1996 |pmid= 8755926 |doi= | pmc=1914712 }}
*{{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 }}
*{{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 | author=Hellenbroich Y, Bubel S, Pawlack H, ''et al.'' |title=Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. |journal=J. Neurol. |volume=250 |issue= 6 |pages= 668–71 |year= 2003 |pmid= 12796826 |doi= 10.1007/s00415-003-1052-x }}
*{{cite journal   |vauthors=Hellenbroich Y, Bubel S, Pawlack H, etal |title=Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. |journal=J. Neurol. |volume=250 |issue= 6 |pages= 668–71 |year= 2003 |pmid= 12796826 |doi= 10.1007/s00415-003-1052-x }}
*{{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 }}
*{{cite journal   |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |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 }}
*{{cite journal | author=Hirano R, Takashima H, Okubo R, ''et al.'' |title=Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. |journal=Neurogenetics |volume=5 |issue= 4 |pages= 215–21 |year= 2005 |pmid= 15455264 |doi= 10.1007/s10048-004-0194-z }}
*{{cite journal   |vauthors=Hirano R, Takashima H, Okubo R, etal |title=Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. |journal=Neurogenetics |volume=5 |issue= 4 |pages= 215–21 |year= 2005 |pmid= 15455264 |doi= 10.1007/s10048-004-0194-z }}
*{{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 }}
*{{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 | author=Ishikawa K, Toru S, Tsunemi T, ''et al.'' |title=An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains. |journal=Am. J. Hum. Genet. |volume=77 |issue= 2 |pages= 280–96 |year= 2005 |pmid= 16001362 |doi= 10.1086/432518 }}
*{{cite journal   |vauthors=Lim J, Hao T, Shaw C, etal |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 }}
*{{cite journal  | author=Wieczorek S, Arning L, Alheite I, Epplen JT |title=Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population. |journal=J. Hum. Genet. |volume=51 |issue= 4 |pages= 363–7 |year= 2006 |pmid= 16491300 |doi= 10.1007/s10038-006-0372-y }}
*{{cite journal   |vauthors=Ouyang Y, Sakoe K, Shimazaki H, etal |title=16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study. |journal=J. Neurol. Sci. |volume=247 |issue= 2 |pages= 180–6 |year= 2006 |pmid= 16780885 |doi= 10.1016/j.jns.2006.04.009 }}
*{{cite journal | author=Lim J, Hao T, Shaw C, ''et al.'' |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 }}
*{{cite journal   |vauthors=Nozaki H, Ikeuchi T, Kawakami A, etal |title=Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. |journal=Mov. Disord. |volume=22 |issue= 6 |pages= 857–62 |year= 2007 |pmid= 17357132 |doi= 10.1002/mds.21443 }}
*{{cite journal | author=Ouyang Y, Sakoe K, Shimazaki H, ''et al.'' |title=16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study. |journal=J. Neurol. Sci. |volume=247 |issue= 2 |pages= 180–6 |year= 2006 |pmid= 16780885 |doi= 10.1016/j.jns.2006.04.009 }}
*{{cite journal   |vauthors=Amino T, Ishikawa K, Toru S, etal |title=Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia. |journal=J. Hum. Genet. |volume=52 |issue= 8 |pages= 643–9 |year= 2007 |pmid= 17611710 |doi= 10.1007/s10038-007-0154-1 }}
*{{cite journal | author=Nozaki H, Ikeuchi T, Kawakami A, ''et al.'' |title=Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. |journal=Mov. Disord. |volume=22 |issue= 6 |pages= 857–62 |year= 2007 |pmid= 17357132 |doi= 10.1002/mds.21443 }}
*{{cite journal | author=Amino T, Ishikawa K, Toru S, ''et al.'' |title=Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia. |journal=J. Hum. Genet. |volume=52 |issue= 8 |pages= 643–9 |year= 2007 |pmid= 17611710 |doi= 10.1007/s10038-007-0154-1 }}
}}
}}
{{refend}}
{{refend}}


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Latest revision as of 18:18, 7 September 2017

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

n/a

n/a

Ensembl

n/a

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UniProt

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n/a

RefSeq (mRNA)

n/a

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RefSeq (protein)

n/a

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

Puratrophin-1 is a protein that in humans is encoded by the PLEKHG4 gene.[1][2][3]

References

  1. ↑ Wieczorek S, Arning L, Alheite I, Epplen JT (Apr 2006). "Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population". J Hum Genet. 51 (4): 363–7. doi:10.1007/s10038-006-0372-y. PMID 16491300.
  2. ↑ Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H (Jul 2005). "An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains". Am J Hum Genet. 77 (2): 280–96. doi:10.1086/432518. PMC 1224530. PMID 16001362.
  3. ↑ "Entrez Gene: PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4".

Further reading



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