Matches in DBpedia 2014 for { <http://dbpedia.org/resource/WHSC1> ?p ?o. }
Showing items 1 to 21 of
21
with 100 items per page.
- WHSC1 abstract "Probable histone-lysine N-methyltransferase NSD2 is an enzyme that in humans is encoded by the WHSC1 gene.This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.".
- WHSC1 entrezgene "7468".
- WHSC1 wikiPageID "14774871".
- WHSC1 wikiPageRevisionID "593313041".
- WHSC1 hasPhotoCollection WHSC1.
- WHSC1 requireManualInspection "no".
- WHSC1 summaryText "This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA decay candidates, hence not represented as reference sequences.".
- WHSC1 updateCitations "yes".
- WHSC1 updatePage "yes".
- WHSC1 updateProteinBox "yes".
- WHSC1 updateSummary "yes".
- WHSC1 type Biomolecule.
- WHSC1 type Protein.
- WHSC1 type BiologicalObject.
- WHSC1 comment "Probable histone-lysine N-methyltransferase NSD2 is an enzyme that in humans is encoded by the WHSC1 gene.This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4.".
- WHSC1 label "WHSC1".
- WHSC1 sameAs m.03gxlkd.
- WHSC1 sameAs Q7950418.
- WHSC1 sameAs Q7950418.
- WHSC1 wasDerivedFrom WHSC1?oldid=593313041.
- WHSC1 isPrimaryTopicOf WHSC1.