Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/FBXW4> ?p ?o }
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- FBXW4 abstract "F-box/WD repeat-containing protein 4 is a protein that in humans is encoded by the FBXW4 gene.This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22.".
- FBXW4 entrezgene "6468".
- FBXW4 wikiPageID "14875513".
- FBXW4 wikiPageLength "6909".
- FBXW4 wikiPageOutDegree "2".
- FBXW4 wikiPageRevisionID "661023757".
- FBXW4 wikiPageWikiLink Gene.
- FBXW4 wikiPageWikiLink Protein.
- FBXW4 wikiPageWikiLinkText "FBXW4".
- FBXW4 requireManualInspection "no".
- FBXW4 summaryText "This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22.".
- FBXW4 updateCitations "yes".
- FBXW4 updatePage "yes".
- FBXW4 updateProteinBox "yes".
- FBXW4 updateSummary "yes".
- FBXW4 wikiPageUsesTemplate Template:Cite_journal.
- FBXW4 wikiPageUsesTemplate Template:Gene-10-stub.
- FBXW4 wikiPageUsesTemplate Template:PBB.
- FBXW4 wikiPageUsesTemplate Template:PBB_Controls.
- FBXW4 wikiPageUsesTemplate Template:PBB_Further_reading.
- FBXW4 wikiPageUsesTemplate Template:PBB_Summary.
- FBXW4 wikiPageUsesTemplate Template:Refbegin.
- FBXW4 wikiPageUsesTemplate Template:Refend.
- FBXW4 wikiPageUsesTemplate Template:Reflist.
- FBXW4 hypernym Protein.
- FBXW4 type Biomolecule.
- FBXW4 type Protein.
- FBXW4 type Thing.
- FBXW4 type Q206229.
- FBXW4 type Q8054.
- FBXW4 comment "F-box/WD repeat-containing protein 4 is a protein that in humans is encoded by the FBXW4 gene.This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation.".
- FBXW4 label "FBXW4".
- FBXW4 sameAs Q18031486.
- FBXW4 sameAs m.03g_v_s.
- FBXW4 sameAs Q18031486.
- FBXW4 wasDerivedFrom FBXW4?oldid=661023757.
- FBXW4 isPrimaryTopicOf FBXW4.