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          See other WHSC1 SIRNA Assays ›
          Gene Symbol:
          WHSC1
          Gene Name:
          Wolf-Hirschhorn syndrome candidate 1
          Gene Aliases:
          MMSET, NSD2, REIIBP, TRX5, WHS
          Chromosome Location:
          Chr.4: 1871357 - 1982207 on Build GRCh38
          UniGene ID:
          Hs.113876
          Species:
          Human
          Species Specific ID (Flybase ID):
          -
          siRNA ID s526860

          Purification
          Size
          Availability Inventoried
          Catalog # 4392420
          Price
          Your Price
          Online offer:
          Check your price ›
          • Genomic Map
          • siRNA Details
          • More Information

          Genomic Map

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          siRNA Details

          Gene Symbol: WHSC1
          Interrogated Sequence Translated Protein Targeted Exon(s) siRNA Location IMAGE Clone ID
          RefSeq NM_001042424.2 NP_001035889.1 17 3204
          NM_133330.2 NP_579877.1 19 3522
          NM_133331.2 NP_579878.1 18 3342
          NM_133335.3 NP_579890.1 17 3167
          XM_005248001.3 XP_005248058.1 17 3147
          XM_005248002.2 XP_005248059.1 15 3036
          XM_011513557.2 XP_011511859.1 17 3083
          XM_011513560.2 XP_011511862.1 6 785
          XM_017008587.1 XP_016864076.1 8 1050
          XM_017008588.1 XP_016864077.1 7 1780
          GenBank mRNA AB029013.1 - 7 1594
          AF071593.1 - 16 3057
          AF083386.1 - 19 3522
          AF083387.1 - 18 3342
          AF083388.1 - 17 3166
          AF083389.1 - 20 3749
          AF083390.1 - 20 3616
          AF330040.1 - 9 1645
          AJ007042.1 - 17 3790
          AK026939.1 - 1 26
          BC094825.1 - 5 695
          BC144464.1 - 8 950
          BC152412.1 - 7 1629 8862517

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          More Information


          Gene Ontology Categories:

          Function(s) Process(es)

          negative regulation of transcription from RNA polymerase II promoter
          membranous septum morphogenesis
          atrial septum primum morphogenesis
          atrial septum secundum morphogenesis
          double-strand break repair via nonhomologous end joining
          transcription, DNA-templated
          anatomical structure morphogenesis
          histone H3-K36 methylation
          chromatin modification
          histone H4-K20 methylation
          positive regulation of isotype switching to IgA isotypes
          bone development
          regulation of establishment of protein localization
          regulation of double-strand break repair via nonhomologous end joining
          chromatin binding
          protein binding
          zinc ion binding
          histone-lysine N-methyltransferase activity
          histone methyltransferase activity (H4-K20 specific)
          sequence-specific DNA binding

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