RAB33B: Difference between revisions

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{{Infobox_gene}}
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'''Ras-related protein Rab-33B''' is a [[protein]] that in humans is encoded by the ''RAB33B'' [[gene]].<ref name="entrez">{{cite web RAB33B, member RAS oncogene family| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=83452| accessdate = }}</ref>
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Mutations in this gene have been associated to cases of [[Dyggve-Melchior-Clausen]] syndrome.<ref name="pmid22652534">{{cite journal | vauthors = Alshammari MJ, Al-Otaibi L, Alkuraya FS | title = Mutation in RAB33B, which encodes a regulator of retrograde Golgi transport, defines a second Dyggve-Melchior-Clausen locus | journal = J Med Genet | volume = 49| issue = 7| pages = 455–61|date=May 2012 | pmid = 22652534 | doi = 10.1136/jmedgenet-2011-100666 }}</ref>
{{GNF_Protein_box
| image = PBB_Protein_RAB33B_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1z06.
| PDB = {{PDB2|1z06}}, {{PDB2|2g77}}
| Name = RAB33B, member RAS oncogene family
| HGNCid = 16075
| Symbol = RAB33B
| AltSymbols =; DKFZP434G099; MGC138182
| OMIM = 605950
| ECnumber = 
| Homologene = 9642
| MGIid = 1330805
| GeneAtlas_image1 = PBB_GE_RAB33B_221014_s_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}}{{GNF_GO|id=GO:0005525 |text = GTP binding}}
| Component = {{GNF_GO|id=GO:0005794 |text = Golgi apparatus}}
| Process = {{GNF_GO|id=GO:0007264 |text = small GTPase mediated signal transduction}} {{GNF_GO|id=GO:0015031 |text = protein transport}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 83452
    | Hs_Ensembl = ENSG00000172007
    | Hs_RefseqProtein = NP_112586
    | Hs_RefseqmRNA = NM_031296
    | Hs_GenLoc_db =
    | Hs_GenLoc_chr = 4
    | Hs_GenLoc_start = 140594411
    | Hs_GenLoc_end = 140616511
    | Hs_Uniprot = Q9H082
    | Mm_EntrezGene = 19338
    | Mm_Ensembl = ENSMUSG00000027739
    | Mm_RefseqmRNA = NM_016858
    | Mm_RefseqProtein = NP_058554
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 3
    | Mm_GenLoc_start = 51571895
    | Mm_GenLoc_end = 51583833
    | Mm_Uniprot = Q0PD21
  }}
}}
'''RAB33B, member RAS oncogene family''', also known as '''RAB33B''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: RAB33B RAB33B, member RAS oncogene family| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=83452| accessdate = }}</ref>


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==References==
{{PBB_Summary
{{reflist}}
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==References==
{{reflist|2}}
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
*{{cite journal   |vauthors=Hillier LW, Graves TA, Fulton RS, etal |title=Generation and annotation of the DNA sequences of human chromosomes 2 and 4. |journal=Nature |volume=434 |issue= 7034 |pages= 724–31 |year= 2005 |pmid= 15815621 |doi= 10.1038/nature03466 }}
| citations =
*{{cite journal   |vauthors=Barrios-Rodiles M, Brown KR, Ozdamar B, etal |title=High-throughput mapping of a dynamic signaling network in mammalian cells. |journal=Science |volume=307 |issue= 5715 |pages= 1621–5 |year= 2005 |pmid= 15761153 |doi= 10.1126/science.1105776 }}
*{{cite journal | author=Hillier LW, Graves TA, Fulton RS, ''et al.'' |title=Generation and annotation of the DNA sequences of human chromosomes 2 and 4. |journal=Nature |volume=434 |issue= 7034 |pages= 724-31 |year= 2005 |pmid= 15815621 |doi= 10.1038/nature03466 }}
*{{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=Barrios-Rodiles M, Brown KR, Ozdamar B, ''et al.'' |title=High-throughput mapping of a dynamic signaling network in mammalian cells. |journal=Science |volume=307 |issue= 5715 |pages= 1621-5 |year= 2005 |pmid= 15761153 |doi= 10.1126/science.1105776 }}
*{{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=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=Valsdottir R, Hashimoto H, Ashman K, etal |title=Identification of rabaptin-5, rabex-5, and GM130 as putative effectors of rab33b, a regulator of retrograde traffic between the Golgi apparatus and ER. |journal=FEBS Lett. |volume=508 |issue= 2 |pages= 201–9 |year= 2001 |pmid= 11718716 |doi=10.1016/S0014-5793(01)02993-3 }}
*{{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=Simpson JC, Wellenreuther R, Poustka A, etal |title=Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. |journal=EMBO Rep. |volume=1 |issue= 3 |pages= 287–92 |year= 2001 |pmid= 11256614 |doi= 10.1093/embo-reports/kvd058 | pmc=1083732 }}
*{{cite journal | author=Valsdottir R, Hashimoto H, Ashman K, ''et al.'' |title=Identification of rabaptin-5, rabex-5, and GM130 as putative effectors of rab33b, a regulator of retrograde traffic between the Golgi apparatus and ER. |journal=FEBS Lett. |volume=508 |issue= 2 |pages= 201-9 |year= 2001 |pmid= 11718716 |doi=  }}
*{{cite journal   |vauthors=Wiemann S, Weil B, Wellenreuther R, etal |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422–35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.GR1547R  | pmc=311072 }}
*{{cite journal | author=Simpson JC, Wellenreuther R, Poustka A, ''et al.'' |title=Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. |journal=EMBO Rep. |volume=1 |issue= 3 |pages= 287-92 |year= 2001 |pmid= 11256614 |doi= 10.1093/embo-reports/kvd058 }}
*{{cite journal   |vauthors=Zheng JY, Koda T, Fujiwara T, etal |title=A novel Rab GTPase, Rab33B, is ubiquitously expressed and localized to the medial Golgi cisternae. |journal=J. Cell Sci. |volume=111 |issue=  8|pages= 1061–9 |year= 1998 |pmid= 9512502 |doi=  }}
*{{cite journal | author=Wiemann S, Weil B, Wellenreuther R, ''et al.'' |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422-35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.154701 }}
*{{cite journal | author=Zheng JY, Koda T, Fujiwara T, ''et al.'' |title=A novel Rab GTPase, Rab33B, is ubiquitously expressed and localized to the medial Golgi cisternae. |journal=J. Cell. Sci. |volume=111 ( Pt 8) |issue=  |pages= 1061-9 |year= 1998 |pmid= 9512502 |doi=  }}
}}
{{refend}}
{{refend}}
{{PDB Gallery|geneid=83452}}


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Latest revision as of 20:41, 8 November 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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n/a

RefSeq (protein)

n/a

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

Ras-related protein Rab-33B is a protein that in humans is encoded by the RAB33B gene.[1]

Mutations in this gene have been associated to cases of Dyggve-Melchior-Clausen syndrome.[2]

References

  1. Template:Cite web RAB33B, member RAS oncogene family
  2. Alshammari MJ, Al-Otaibi L, Alkuraya FS (May 2012). "Mutation in RAB33B, which encodes a regulator of retrograde Golgi transport, defines a second Dyggve-Melchior-Clausen locus". J Med Genet. 49 (7): 455–61. doi:10.1136/jmedgenet-2011-100666. PMID 22652534.

Further reading