Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/WNT1> ?p ?o }
Showing triples 1 to 44 of
44
with 100 triples per page.
- WNT1 abstract "Proto-oncogene protein Wnt-1 is a protein that in humans is encoded by the WNT1 gene.The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.".
- WNT1 entrezgene "7471".
- WNT1 wikiPageID "14149813".
- WNT1 wikiPageLength "9284".
- WNT1 wikiPageOutDegree "6".
- WNT1 wikiPageRevisionID "687944990".
- WNT1 wikiPageWikiLink Cerebellum.
- WNT1 wikiPageWikiLink Gene.
- WNT1 wikiPageWikiLink Joubert_syndrome.
- WNT1 wikiPageWikiLink Midbrain.
- WNT1 wikiPageWikiLink Protein.
- WNT1 wikiPageWikiLink Wnt_signaling_pathway.
- WNT1 wikiPageWikiLinkText "WNT1".
- WNT1 wikiPageWikiLinkText "Wnt1".
- WNT1 requireManualInspection "no".
- WNT1 summaryText "The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.".
- WNT1 updateCitations "yes".
- WNT1 updatePage "yes".
- WNT1 updateProteinBox "yes".
- WNT1 updateSummary "yes".
- WNT1 wikiPageUsesTemplate Template:Cite_journal.
- WNT1 wikiPageUsesTemplate Template:Gene-12-stub.
- WNT1 wikiPageUsesTemplate Template:PBB.
- WNT1 wikiPageUsesTemplate Template:PBB_Controls.
- WNT1 wikiPageUsesTemplate Template:PBB_Further_reading.
- WNT1 wikiPageUsesTemplate Template:PBB_Summary.
- WNT1 wikiPageUsesTemplate Template:Refbegin.
- WNT1 wikiPageUsesTemplate Template:Refend.
- WNT1 wikiPageUsesTemplate Template:Reflist.
- WNT1 wikiPageUsesTemplate Template:Wnt_signaling_pathway.
- WNT1 hypernym Protein.
- WNT1 type Biomolecule.
- WNT1 type Protein.
- WNT1 type Thing.
- WNT1 type Q206229.
- WNT1 type Q8054.
- WNT1 comment "Proto-oncogene protein Wnt-1 is a protein that in humans is encoded by the WNT1 gene.The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family.".
- WNT1 label "WNT1".
- WNT1 sameAs Q18032358.
- WNT1 sameAs Wnt1.
- WNT1 sameAs m.03cw4cc.
- WNT1 sameAs Q18032358.
- WNT1 wasDerivedFrom WNT1?oldid=687944990.
- WNT1 isPrimaryTopicOf WNT1.