Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/RFX5> ?p ?o }
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- RFX5 abstract "DNA-binding protein RFX5 is a protein that in humans is encoded by the RFX5 gene.A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined.".
- RFX5 entrezgene "5993".
- RFX5 wikiPageID "14774442".
- RFX5 wikiPageLength "11203".
- RFX5 wikiPageOutDegree "5".
- RFX5 wikiPageRevisionID "621466431".
- RFX5 wikiPageWikiLink CIITA.
- RFX5 wikiPageWikiLink Category:Transcription_factors.
- RFX5 wikiPageWikiLink Gene.
- RFX5 wikiPageWikiLink Protein.
- RFX5 wikiPageWikiLink Protein-protein_interaction.
- RFX5 wikiPageWikiLink Protein–protein_interaction.
- RFX5 wikiPageWikiLinkText "5".
- RFX5 wikiPageWikiLinkText "RFX5".
- RFX5 wikiPageWikiLinkText "X5".
- RFX5 hasPhotoCollection RFX5.
- RFX5 requireManualInspection "no".
- RFX5 summaryText "A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome . At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX . RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined.".
- RFX5 updateCitations "yes".
- RFX5 updatePage "yes".
- RFX5 updateProteinBox "yes".
- RFX5 updateSummary "yes".
- RFX5 wikiPageUsesTemplate Template:FactorBook.
- RFX5 wikiPageUsesTemplate Template:Gene-1-stub.
- RFX5 wikiPageUsesTemplate Template:MeshName.
- RFX5 wikiPageUsesTemplate Template:NLM_content.
- RFX5 wikiPageUsesTemplate Template:PBB.
- RFX5 wikiPageUsesTemplate Template:PBB_Controls.
- RFX5 wikiPageUsesTemplate Template:PBB_Further_reading.
- RFX5 wikiPageUsesTemplate Template:PBB_Summary.
- RFX5 wikiPageUsesTemplate Template:Refbegin.
- RFX5 wikiPageUsesTemplate Template:Refend.
- RFX5 wikiPageUsesTemplate Template:Reflist.
- RFX5 wikiPageUsesTemplate Template:Transcription_factors.
- RFX5 subject Category:Transcription_factors.
- RFX5 hypernym Protein.
- RFX5 type Article.
- RFX5 type Biomolecule.
- RFX5 type Protein.
- RFX5 type Article.
- RFX5 type Factor.
- RFX5 type Institute.
- RFX5 type Source.
- RFX5 type Thing.
- RFX5 type Q206229.
- RFX5 type Q8054.
- RFX5 comment "DNA-binding protein RFX5 is a protein that in humans is encoded by the RFX5 gene.A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS.".
- RFX5 label "RFX5".
- RFX5 sameAs m.03gxl3z.
- RFX5 sameAs Q7276603.
- RFX5 sameAs Q7276603.
- RFX5 wasDerivedFrom RFX5?oldid=621466431.
- RFX5 isPrimaryTopicOf RFX5.