UTP6: Difference between revisions

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{{Infobox_gene}}
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'''U3 small nucleolar RNA-associated protein 6 homolog''' is a [[protein]] that in humans is encoded by the ''UTP6'' [[gene]].<ref name="pmid10843809">{{cite journal | vauthors = Jenne DE, Tinschert S, Stegmann E, Reimann H, Nurnberg P, Horn D, Naumann I, Buske A, Thiel G | title = A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions | journal = Genomics | volume = 66 | issue = 1 | pages = 93–7 |date=Jul 2000 | pmid = 10843809 | pmc =  | doi = 10.1006/geno.2000.6179 }}</ref><ref name="pmid16138909">{{cite journal | vauthors = Venturin M, Bentivegna A, Moroni R, Larizza L, Riva P | title = Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval | journal = Ann Hum Genet | volume = 69 | issue = Pt 5 | pages = 508–16 |date=Sep 2005 | pmid = 16138909 | pmc =  | doi = 10.1111/j.1529-8817.2005.00203.x }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: UTP6 UTP6, small subunit (SSU) processome component, homolog (yeast)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55813| accessdate = }}</ref>
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{{GNF_Protein_box
| image =
| image_source = 
| PDB =
| Name = UTP6, small subunit (SSU) processome component, homolog (yeast)
| HGNCid = 18279
| Symbol = UTP6
| AltSymbols =; C17orf40; HCA66
| OMIM =
| ECnumber =
| Homologene = 41265
| MGIid = 2445193
| GeneAtlas_image1 = PBB_GE_UTP6_218715_at_tn.png
  | Function = {{GNF_GO|id=GO:0005515 |text = protein binding}}  
| Component = {{GNF_GO|id=GO:0005622 |text = intracellular}} {{GNF_GO|id=GO:0005634 |text = nucleus}}
| Process = {{GNF_GO|id=GO:0006364 |text = rRNA processing}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 55813
    | Hs_Ensembl = ENSG00000108651
    | Hs_RefseqProtein = NP_060898
    | Hs_RefseqmRNA = NM_018428
    | Hs_GenLoc_db =   
    | Hs_GenLoc_chr = 17
    | Hs_GenLoc_start = 27214303
    | Hs_GenLoc_end = 27252842
    | Hs_Uniprot = Q9NYH9
    | Mm_EntrezGene = 216987
    | Mm_Ensembl = ENSMUSG00000035575
    | Mm_RefseqmRNA = NM_144826
    | Mm_RefseqProtein = NP_659075
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 11
    | Mm_GenLoc_start = 79750151
    | Mm_GenLoc_end = 79778582
    | Mm_Uniprot = Q3TE84
  }}
}}
'''UTP6, small subunit (SSU) processome component, homolog (yeast)''', also known as '''UTP6''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: UTP6 UTP6, small subunit (SSU) processome component, homolog (yeast)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55813| accessdate = }}</ref>


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| summary_text =  
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==See also==
{{colbegin|3}}
* [[Fibrillarin]]
* [[Small nucleolar RNA U3]]
* [[RCL1]]
* [[RRP9]]
* [[UTP11L]]
* [[UTP14A]]
* [[UTP15]]
{{colend}}


==References==
==References==
{{reflist|2}}
{{reflist}}
 
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal  | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171-4 |year= 1994 |pmid= 8125298 |doi=  }}
*{{cite journal  | vauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }}
*{{cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149-56 |year= 1997 |pmid= 9373149 |doi=  }}
*{{cite journal   |vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3  }}
*{{cite journal  | author=Jenne DE, Tinschert S, Stegmann E, ''et al.'' |title=A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions. |journal=Genomics |volume=66 |issue= 1 |pages= 93-7 |year= 2000 |pmid= 10843809 |doi= 10.1006/geno.2000.6179 }}
*{{cite journal   |vauthors=Wang Y, Han KJ, Pang XW, etal |title=Large scale identification of human hepatocellular carcinoma-associated antigens by autoantibodies. |journal=J. Immunol. |volume=169 |issue= 2 |pages= 1102–9 |year= 2002 |pmid= 12097419 |doi=  10.4049/jimmunol.169.2.1102}}
*{{cite journal | author=Wang Y, Han KJ, Pang XW, ''et al.'' |title=Large scale identification of human hepatocellular carcinoma-associated antigens by autoantibodies. |journal=J. Immunol. |volume=169 |issue= 2 |pages= 1102-9 |year= 2002 |pmid= 12097419 |doi=  }}
*{{cite journal   |vauthors=Scherl A, Couté Y, Déon C, etal |title=Functional proteomic analysis of human nucleolus. |journal=Mol. Biol. Cell |volume=13 |issue= 11 |pages= 4100–9 |year= 2003 |pmid= 12429849 |doi= 10.1091/mbc.E02-05-0271 | pmc=133617 }}
*{{cite journal | author=Scherl A, Couté Y, Déon C, ''et al.'' |title=Functional proteomic analysis of human nucleolus. |journal=Mol. Biol. Cell |volume=13 |issue= 11 |pages= 4100-9 |year= 2003 |pmid= 12429849 |doi= 10.1091/mbc.E02-05-0271 }}
*{{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=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=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=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=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=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=Andersen JS, Lam YW, Leung AK, etal |title=Nucleolar proteome dynamics. |journal=Nature |volume=433 |issue= 7021 |pages= 77–83 |year= 2005 |pmid= 15635413 |doi= 10.1038/nature03207 }}
*{{cite journal | author=Andersen JS, Lam YW, Leung AK, ''et al.'' |title=Nucleolar proteome dynamics. |journal=Nature |volume=433 |issue= 7021 |pages= 77-83 |year= 2005 |pmid= 15635413 |doi= 10.1038/nature03207 }}
*{{cite journal   |vauthors=Rual JF, Venkatesan K, Hao T, etal |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal | author=Venturin M, Bentivegna A, Moroni R, ''et al.'' |title=Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval. |journal=Ann. Hum. Genet. |volume=69 |issue= Pt 5 |pages= 508-16 |year= 2005 |pmid= 16138909 |doi= 10.1111/j.1529-8817.2005.00203.x }}
*{{cite journal   |vauthors=Piddubnyak V, Rigou P, Michel L, etal |title=Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients. |journal=Cell Death Differ. |volume=14 |issue= 6 |pages= 1222–33 |year= 2007 |pmid= 17380155 |doi= 10.1038/sj.cdd.4402122 }}
*{{cite journal  | author=Rual JF, Venkatesan K, Hao T, ''et al.'' |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173-8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal   |vauthors=Douglas J, Cilliers D, Coleman K, etal |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083 }}
*{{cite journal | author=Piddubnyak V, Rigou P, Michel L, ''et al.'' |title=Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients. |journal=Cell Death Differ. |volume=14 |issue= 6 |pages= 1222-33 |year= 2007 |pmid= 17380155 |doi= 10.1038/sj.cdd.4402122 }}
*{{cite journal | author=Douglas J, Cilliers D, Coleman K, ''et al.'' |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963-5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083 }}
}}
}}
{{refend}}
{{refend}}


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Revision as of 10:23, 17 September 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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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

U3 small nucleolar RNA-associated protein 6 homolog is a protein that in humans is encoded by the UTP6 gene.[1][2][3]


See also

References

  1. ↑ Jenne DE, Tinschert S, Stegmann E, Reimann H, Nurnberg P, Horn D, Naumann I, Buske A, Thiel G (Jul 2000). "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions". Genomics. 66 (1): 93–7. doi:10.1006/geno.2000.6179. PMID 10843809.
  2. ↑ Venturin M, Bentivegna A, Moroni R, Larizza L, Riva P (Sep 2005). "Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval". Ann Hum Genet. 69 (Pt 5): 508–16. doi:10.1111/j.1529-8817.2005.00203.x. PMID 16138909.
  3. ↑ "Entrez Gene: UTP6 UTP6, small subunit (SSU) processome component, homolog (yeast)".

Further reading



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