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          • Home
          • › Search Tool
          • › Search Results
          • › Hs04923594_cn
          See other HMGN3 CNV Assays ›
          Gene Symbol
          HMGN3
          Assay Reference Genome
          Location

          Chr.6:79209398 on build GRCh38
          Cytoband
          6q14.1
          Assay ID Hs04923594_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          9324

          Gene Name:

          high mobility group nucleosomal binding domain 3

          Gene Aliases:

          PNAS-24, PNAS-25, TRIP7

          Location:

          Chr.6:79201245-79234738 on Build GRCh38

          Assay Gene Location:

          Within Intron 2
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          HMGN3 NM_001201362.1 NP_001188291.1
          NM_001201363.1 NP_001188292.1
          NM_001318884.1 NP_001305813.1
          NM_001318885.1 NP_001305814.1
          NM_001318886.1 NP_001305815.1
          NM_001318887.1 NP_001305816.1
          NM_001318888.1 NP_001305817.1
          NM_004242.3 NP_004233.1
          NM_138730.2 NP_620058.1
          AF274949.1 AAK07526.1
          AF401520.1 AAK92012.1
          AK315391.1
          AY043282.1 AAK85736.1
          BC009529.2 AAH09529.1
          BF790582.1
          BI551210.1
          BM927225.1
          CF553005.1
          CK023734.1
          CX761444.1
          DA894213.1
          L40357.1 AAA73877.1
          W19124.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv3609679 Chr.6:79085485 - 79214414 on Build GRCh38 Loss HMGN3
          esv3609684 Chr.6:79190181 - 79214854 on Build GRCh38 Loss HMGN3
          nsv830706 Chr.6:79116193 - 79285161 on Build GRCh38 Gain HMGN3-AS1 HMGN3

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Panther Classification:

          Molecular Function -

          chromatin/chromatin-binding, or -regulatory protein

          Gene Ontology Categories:

          Function(s) Process(es)

          biological_process
          covalent chromatin modification
          positive regulation of transcription from RNA polymerase II promoter
          regulation of insulin secretion involved in cellular response to glucose stimulus
          nucleosomal DNA binding
          thyroid hormone receptor binding

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