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          • › Hs07535239_cn
          See other CRIP2 CNV Assays ›
          Gene Symbol
          CRIP2
          Assay Reference Genome
          Location

          Chr.14:105474309 on build GRCh38
          Cytoband
          14q32.33
          Assay ID Hs07535239_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:

          1397

          Gene Name:

          cysteine rich protein 2

          Gene Aliases:

          CRIP, CRP2, ESP1

          Location:

          Chr.14:105472938-105480170 on Build GRCh38

          Assay Gene Location:

          Within Intron 1
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          CRIP2 NM_001270837.1 NP_001257766.1
          NR_073082.1
          AK057837.1
          AK300092.1
          BE271979.1
          HY161884.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          dgv3996n54 Chr.14:105474226 - 105488519 on Build GRCh38 Gain CRIP2 CRIP1
          nsv566204 Chr.14:105376842 - 105479048 on Build GRCh38 Gain TEX22 CRIP2 LOC100507437 MTA1 PACS2
          nsv566189 Chr.14:105305091 - 105475240 on Build GRCh38 Gain TEX22 CRIP2 LOC100507437 BRF1 MTA1 PACS2
          nsv817647 Chr.14:105382554 - 105480505 on Build GRCh38 Gain TEX22 CRIP2 LOC100507437 MTA1 PACS2
          nsv1160204 Chr.14:105291411 - 105483783 on Build GRCh38 Duplication TEX22 CRIP2 LOC100507437 BRF1 MTA1 PACS2
          dgv3994n54 Chr.14:105474172 - 105477662 on Build GRCh38 Gain CRIP2
          esv21791 Chr.14:105474144 - 105475279 on Build GRCh38 Loss CRIP2
          nsv566206 Chr.14:105439736 - 105543235 on Build GRCh38 Loss CRIP2 C14orf80 LOC105370697 MTA1 CRIP1 TMEM121
          nsv832890 Chr.14:105304955 - 105483089 on Build GRCh38 Loss TEX22 CRIP2 LOC100507437 BRF1 MTA1 PACS2
          nsv1440 Chr.14:105473170 - 105479862 on Build GRCh38 Insertion CRIP2
          dgv3989n54 Chr.14:105468704 - 105475240 on Build GRCh38 Gain CRIP2 MTA1
          nsv566209 Chr.14:105465248 - 105475240 on Build GRCh38 Gain+Loss CRIP2 MTA1
          nsv827088 Chr.14:105454469 - 105498549 on Build GRCh38 Gain CRIP2 C14orf80 MTA1 CRIP1
          nsv952282 Chr.14:105363764 - 105510163 on Build GRCh38 Deletion TEX22 CRIP2 C14orf80 LOC100507437 MTA1 CRIP1 PACS2
          esv2760014 Chr.14:105047009 - 105483089 on Build GRCh38 Loss GPR132 TEX22 CRIP2 LOC100507437 LOC102723354 BRF1 MIR6765 JAG2 MTA1 BTBD6 NUDT14 PACS2
          dgv3988n54 Chr.14:105466757 - 105477662 on Build GRCh38 Gain CRIP2 MTA1
          nsv470679 Chr.14:105124547 - 105605978 on Build GRCh38 Loss CRIP2 IGHA2 LOC100507437 LOC105370697 IGH JAG2 NUDT14 CRIP1 TEX22 C14orf80 BRF1 MIR6765 MTA1 BTBD6 PACS2 TMEM121
          dgv3987n54 Chr.14:105461599 - 105499970 on Build GRCh38 Loss CRIP2 C14orf80 MTA1 CRIP1
          dgv3997n54 Chr.14:105474383 - 105475240 on Build GRCh38 Loss CRIP2
          nsv1054190 Chr.14:105246882 - 105701138 on Build GRCh38 Gain MIR8071-2 CRIP2 IGHG2 IGHA2 LOC100507437 LOC105370697 IGH MIR8071-1 CRIP1 TEX22 IGHG4 ELK2AP C14orf80 BRF1 MTA1 BTBD6 PACS2 TMEM121
          esv3635645 Chr.14:105473682 - 105484540 on Build GRCh38 Gain CRIP2
          nsv517055 Chr.14:105136282 - 106779068 on Build GRCh38 Gain+Loss IGHG1 MIR8071-2 CRIP2 IGHV3-30 IGHA2 LOC100507437 LOC105370697 MIR8071-1 NUDT14 IGHV3-23 IGHA1 IGHG4 C14orf80 IGHV1-69 KIAA0125 LINC00221 IGHV4-31 MTA1 BTBD6 MIR4537 IGHG3 MIR4507 PACS2 TMEM121 ADAM6 IGHM IGHG2 IGH JAG2 IGHV3-69-1 IGHD MIR4539 CRIP1 TEX22 IGHV4-55 IGHV3-41 ELK2AP IGHV3-71 BRF1 LOC107987211 MIR6765 IGHV3-48 LINC00226 MIR4538
          nsv566220 Chr.14:105472502 - 105475240 on Build GRCh38 Gain+Loss CRIP2

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Panther Classification:

          Molecular Function -

          actin or actin-binding cytoskeletal protein

          Gene Ontology Categories:

          Function(s) Process(es)

          positive regulation of cell proliferation
          hemopoiesis
          zinc ion binding

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