RPGRIP1L: Difference between revisions

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{{protein
{{infobox protein
|Name=RPGRIP1-like
|Name=RPGRIP1-like
|caption=
|caption=
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|HGNCid=29168
|HGNCid=29168
|Symbol=RPGRIP1L
|Symbol=RPGRIP1L
|AltSymbols=NPHP8, KIAA1005, CORS3, JBTS7, MKS5
|AltSymbols=NPHP8, KIAA1005, CORS3, JBTS7, MKS5, FTM
|EntrezGene=23322
|EntrezGene=23322
|OMIM= 610937
|OMIM= 610937
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|LocusSupplementaryData=
|LocusSupplementaryData=
}}
}}
{{SI}}
'''RPGRIP1L''' is a human [[gene]].<ref name="pmid10231032"/>
 
 
'''RPGRIP1L''' is a human [[gene]].<ref name="pmid10231032">{{cite journal | author = Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O| title = Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro | journal = DNA research : an international journal for rapid publication of reports on genes and genomes | volume = 6 | issue = 1 | pages = 63–70 | year = 1999 | month = February | pmid = 10231032 | doi = 10.1093/dnares/6.1.63 | url = | issn = }}</ref>


==Function==
==Function==


The protein encoded by this gene is localized to primary [[cilia]] and [[centrosome]]s in ciliated human epithelial kidney cells. RPGRIP1L colocalized at the basal body-centrosome complex with the proteins [[NPHP4]], [[NPHP6]], and [[Microtubule nucleation|TUBG1]].<ref name="pmid17558409">{{cite journal | author = Delous M, Baala L, Salomon R, Laclef C, Vierkotten J, Tory K, Golzio C, Lacoste T, Besse L, Ozilou C, Moutkine I, Hellman NE, Anselme I, Silbermann F, Vesque C, Gerhardt C, Rattenberry E, Wolf MT, Gubler MC, Martinovic J, Encha-Razavi F, Boddaert N, Gonzales M, Macher MA, Nivet H, Champion G, Berthélémé JP, Niaudet P, McDonald F, Hildebrandt F, Johnson CA, Vekemans M, Antignac C, Rüther U, Schneider-Maunoury S, Attié-Bitach T, Saunier S | title = The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome | journal = Nature genetics | volume = 39 | issue = 7 | pages = 875–81 | year = 2007 | month = July | pmid = 17558409 | doi = 10.1038/ng2039 | url = | issn = }}</ref><ref name="pmid17558407">{{cite journal | author =Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Märker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R | title = Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome | journal = Nature genetics | volume = 39 | issue = 7 | pages = 882–8 | year = 2007 | month = July | pmid = 17558407 | doi = 10.1038/ng2069 | url = | issn = }}</ref>
The protein encoded by this gene is localized to primary [[cilia]] and [[centrosome]]s in ciliated human epithelial kidney cells and retinal pigment epithelial cells . RPGRIP1L colocalized at the basal body-centrosome complex with the proteins [[NPHP4]], [[NPHP6]], and [[Microtubule nucleation|TUBG1]].<ref name="pmid17558409"/><ref name="pmid17558407"/>
Also, it can interact with MyosinVa <ref> Assis, L. H. P. et al. The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L. Sci. Rep. 7, 43692; doi: 10.1038/srep43692 (2017)</ref>


==Clinical significance==
==Clinical significance==


Mutations in the RPGRIP1L gene are associated with [[Joubert syndrome]] and [[Meckel syndrome]] which belong to a group of developmental [[autosomal recessive]] disorders that are associated with [[cilium]] dysfunction.<ref name="pmid17558409"/> Mutations in this gene are also associated with [[nephronophthisis]].<ref name="pmid18281315">{{cite journal | author = Devuyst O, Arnould VJ | title = Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies | journal = Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | volume = 23 | issue = 5 | pages = 1500–3 | year = 2008 | month = May | pmid = 18281315 | doi = 10.1093/ndt/gfn033 | url = | issn = }}</ref>
Mutations in the RPGRIP1L gene are associated with [[Joubert syndrome]] and [[Meckel syndrome]] which belong to a group of developmental [[autosomal recessive]] disorders that are associated with [[cilium]] dysfunction.<ref name="pmid17558409"/> Mutations in this gene are also associated with [[nephronophthisis]].<ref name="pmid18281315"/> [[Copy number variation]] affecting the gene was associated with [[schizophrenia]] in one study.<ref name="SzGene">[http://www.schizophreniaforum.org/res/sczgene/geneoverview.asp?geneid=736 Gene Overview of All Published Schizophrenia-Association Studies for RPGRIP1L] - [[SzGene]] database at [[Schizophrenia Research Forum]].</ref>
{{-}}
 
==References==
==References==
{{Reflist|refs=


{{Reflist|2}}
<ref name="pmid10231032">{{cite journal | vauthors = Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O | title = Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro | journal = [[DNA Research]] | volume = 6 | issue = 1 | pages = 63–70 |date=February 1999 | pmid = 10231032 | doi = 10.1093/dnares/6.1.63 }}</ref>


<ref name="pmid17558409">{{cite journal | vauthors = Delous M, Baala L, Salomon R, Laclef C, Vierkotten J, Tory K, Golzio C, Lacoste T, Besse L, Ozilou C, Moutkine I, Hellman NE, Anselme I, Silbermann F, Vesque C, Gerhardt C, Rattenberry E, Wolf MT, Gubler MC, Martinovic J, Encha-Razavi F, Boddaert N, Gonzales M, Macher MA, Nivet H, Champion G, Berthélémé JP, Niaudet P, McDonald F, Hildebrandt F, Johnson CA, Vekemans M, Antignac C, Rüther U, Schneider-Maunoury S, Attié-Bitach T, Saunier S | title = The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome | journal = [[Nature Genetics]] | volume = 39 | issue = 7 | pages = 875–81 |date=July 2007 | pmid = 17558409 | doi = 10.1038/ng2039 | url = | issn = }}</ref>
<ref name="pmid17558407">{{cite journal | vauthors = Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Märker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R | title = Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome | journal = [[Nature Genetics]] | volume = 39 | issue = 7 | pages = 882–8 |date=July 2007 | pmid = 17558407 | doi = 10.1038/ng2069 | url = | issn = }}</ref>
<ref name="pmid18281315">{{cite journal | vauthors = Devuyst O, Arnould VJ | title = Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies | journal = Nephrol. Dial. Transplant. | volume = 23 | issue = 5 | pages = 1500–3 |date=May 2008 | pmid = 18281315 | doi = 10.1093/ndt/gfn033 | url = | issn = }}</ref>
}}


{{Ciliary proteins}}




{{WH}}
{{gene-16-stub}}
{{WS}}

Revision as of 11:23, 23 March 2017

RPGRIP1-like
Identifiers
SymbolRPGRIP1L
Alt. symbolsNPHP8, KIAA1005, CORS3, JBTS7, MKS5, FTM
Entrez23322
HUGO29168
OMIM610937
RefSeqNM_015272
UniProtQ68CZ1
Other data
LocusChr. 16 q12.2

RPGRIP1L is a human gene.[1]

Function

The protein encoded by this gene is localized to primary cilia and centrosomes in ciliated human epithelial kidney cells and retinal pigment epithelial cells . RPGRIP1L colocalized at the basal body-centrosome complex with the proteins NPHP4, NPHP6, and TUBG1.[2][3] Also, it can interact with MyosinVa [4]

Clinical significance

Mutations in the RPGRIP1L gene are associated with Joubert syndrome and Meckel syndrome which belong to a group of developmental autosomal recessive disorders that are associated with cilium dysfunction.[2] Mutations in this gene are also associated with nephronophthisis.[5] Copy number variation affecting the gene was associated with schizophrenia in one study.[6]

References

  1. ↑ Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (February 1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 6 (1): 63–70. doi:10.1093/dnares/6.1.63. PMID 10231032.
  2. ↑ 2.0 2.1 Delous M, Baala L, Salomon R, Laclef C, Vierkotten J, Tory K, Golzio C, Lacoste T, Besse L, Ozilou C, Moutkine I, Hellman NE, Anselme I, Silbermann F, Vesque C, Gerhardt C, Rattenberry E, Wolf MT, Gubler MC, Martinovic J, Encha-Razavi F, Boddaert N, Gonzales M, Macher MA, Nivet H, Champion G, Berthélémé JP, Niaudet P, McDonald F, Hildebrandt F, Johnson CA, Vekemans M, Antignac C, Rüther U, Schneider-Maunoury S, Attié-Bitach T, Saunier S (July 2007). "The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome". Nature Genetics. 39 (7): 875–81. doi:10.1038/ng2039. PMID 17558409.
  3. ↑ Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Märker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R (July 2007). "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome". Nature Genetics. 39 (7): 882–8. doi:10.1038/ng2069. PMID 17558407.
  4. ↑ Assis, L. H. P. et al. The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L. Sci. Rep. 7, 43692; doi: 10.1038/srep43692 (2017)
  5. ↑ Devuyst O, Arnould VJ (May 2008). "Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies". Nephrol. Dial. Transplant. 23 (5): 1500–3. doi:10.1093/ndt/gfn033. PMID 18281315.
  6. ↑ Gene Overview of All Published Schizophrenia-Association Studies for RPGRIP1L - SzGene database at Schizophrenia Research Forum.


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