Matches in DBpedia 2014 for { <http://dbpedia.org/resource/SETBP1> ?p ?o. }
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- SETBP1 abstract "SETBP1 is a human gene.It can be associated with Schinzel–Giedion syndrome.In 2012 SETBP1 was identified as a novel oncogene; specific somatic mutations of this gene were discovered in patients affected by atypical Chronic Myeloid Leukemia (aCML) and related diseases. These mutations, which are identical to the ones present in SGS as germ line mutations, impair the degradation of SETBP1 and therefore cause increased cellular levels of the protein.".
- SETBP1 arm "q".
- SETBP1 band "21.1".
- SETBP1 chromosome "18".
- SETBP1 entrezgene "26040".
- SETBP1 hgncid "15573".
- SETBP1 refseq "NM_001130110".
- SETBP1 symbol "SETBP1".
- SETBP1 wikiPageExternalLink 269150?search=number%3A%28269150%20OR%20611060%29&highlight=611060%20269150.
- SETBP1 wikiPageID "29814728".
- SETBP1 wikiPageRevisionID "549472713".
- SETBP1 arm "q".
- SETBP1 band "21.1".
- SETBP1 chromosome "18".
- SETBP1 entrezgene "26040".
- SETBP1 hasPhotoCollection SETBP1.
- SETBP1 hgncid "15573".
- SETBP1 name "SET binding protein 1".
- SETBP1 refseq "NM_001130110".
- SETBP1 symbol "SETBP1".
- SETBP1 type Biomolecule.
- SETBP1 type Protein.
- SETBP1 type BiologicalObject.
- SETBP1 comment "SETBP1 is a human gene.It can be associated with Schinzel–Giedion syndrome.In 2012 SETBP1 was identified as a novel oncogene; specific somatic mutations of this gene were discovered in patients affected by atypical Chronic Myeloid Leukemia (aCML) and related diseases. These mutations, which are identical to the ones present in SGS as germ line mutations, impair the degradation of SETBP1 and therefore cause increased cellular levels of the protein.".
- SETBP1 label "SETBP1".
- SETBP1 sameAs m.0fq1r0_.
- SETBP1 sameAs Q7389878.
- SETBP1 sameAs Q7389878.
- SETBP1 wasDerivedFrom SETBP1?oldid=549472713.
- SETBP1 isPrimaryTopicOf SETBP1.