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          • › Hs00217032_cn
          See other CRIP2 CNV Assays ›
          Gene Symbol
          CRIP2
          Assay Reference Genome
          Location

          Chr.14:105479665 on build GRCh38
          Cytoband
          14q32.33
          Assay ID Hs00217032_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
          Your Price
          Online offer:
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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 Exon 11
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          CRIP2 NM_001270837.1 8 1171 NP_001257766.1
          NM_001270841.1 4 364 NP_001257770.1
          NM_001312.3 8 727 NP_001303.1
          NR_073081.1 6 528
          NR_073082.1 8 703
          NR_073083.1 7 632
          NR_073084.1 8 1480
          NR_073085.1 8 952
          AK057837.1 7 504
          AK091845.1 8 1480
          AK223251.1 8 639 BAD96971.1
          AK300092.1
          AK311402.1
          AK315757.1
          BC000434.2 8 658 AAH00434.1
          BC001931.1 8 658 AAH01931.1
          BC034151.1 8 708 AAH34151.1
          BC128101.1 8 682
          BE271979.1
          BT019911.1 AAV38714.1
          CN367966.1
          D42123.1 8 665 BAA07703.1
          HY078632.1
          U36190.1 8 675 AAB03194.1

          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 CRIP1 CRIP2
          nsv817647 Chr.14:105382554 - 105480505 on Build GRCh38 Gain MTA1 TEX22 LOC100507437 PACS2 CRIP2
          dgv3998n54 Chr.14:105474495 - 105770768 on Build GRCh38 Loss IGHG3 CRIP1 IGHG2 IGHA2 TMEM121 IGHA1 LOC107987211 C14orf80 IGH IGHG4 ELK2AP LOC105370697 MIR8071-2 MIR8071-1 CRIP2 IGHG1
          nsv566229 Chr.14:105474172 - 105483783 on Build GRCh38 Loss CRIP2
          nsv1160204 Chr.14:105291411 - 105483783 on Build GRCh38 Duplication MTA1 BRF1 TEX22 LOC100507437 PACS2 CRIP2
          nsv566206 Chr.14:105439736 - 105543235 on Build GRCh38 Loss LOC105370697 CRIP1 MTA1 TMEM121 C14orf80 CRIP2
          nsv1440 Chr.14:105473170 - 105479862 on Build GRCh38 Insertion CRIP2
          nsv832890 Chr.14:105304955 - 105483089 on Build GRCh38 Loss MTA1 BRF1 TEX22 LOC100507437 PACS2 CRIP2
          nsv566210 Chr.14:105465248 - 105488368 on Build GRCh38 Gain CRIP1 MTA1 CRIP2
          nsv9177 Chr.14:105476516 - 105485998 on Build GRCh38 Gain CRIP2
          nsv827088 Chr.14:105454469 - 105498549 on Build GRCh38 Gain CRIP1 MTA1 C14orf80 CRIP2
          nsv952282 Chr.14:105363764 - 105510163 on Build GRCh38 Deletion CRIP1 MTA1 TEX22 C14orf80 LOC100507437 PACS2 CRIP2
          dgv3999n54 Chr.14:105474867 - 105487998 on Build GRCh38 Loss CRIP1 CRIP2
          esv2760014 Chr.14:105047009 - 105483089 on Build GRCh38 Loss MIR6765 MTA1 BRF1 JAG2 TEX22 NUDT14 LOC100507437 PACS2 BTBD6 CRIP2 GPR132 LOC102723354
          dgv3987n54 Chr.14:105461599 - 105499970 on Build GRCh38 Loss CRIP1 MTA1 C14orf80 CRIP2
          nsv470679 Chr.14:105124547 - 105605978 on Build GRCh38 Loss CRIP1 MTA1 IGHA2 TMEM121 NUDT14 C14orf80 LOC100507437 IGH PACS2 MIR6765 LOC105370697 BRF1 JAG2 TEX22 BTBD6 CRIP2
          esv3635645 Chr.14:105473682 - 105484540 on Build GRCh38 Gain CRIP2
          nsv1054190 Chr.14:105246882 - 105701138 on Build GRCh38 Gain CRIP1 IGHG2 MTA1 IGHA2 TMEM121 C14orf80 LOC100507437 IGH PACS2 IGHG4 ELK2AP LOC105370697 MIR8071-2 BRF1 TEX22 MIR8071-1 BTBD6 CRIP2
          dgv3991n54 Chr.14:105472502 - 105480505 on Build GRCh38 Loss CRIP2
          nsv517055 Chr.14:105136282 - 106779068 on Build GRCh38 Gain+Loss CRIP1 IGHG2 MTA1 MIR4507 TMEM121 IGHA1 IGHV3-69-1 ADAM6 IGHV3-48 LOC100507437 MIR4538 IGHV3-23 MIR6765 MIR8071-2 BRF1 JAG2 IGHV4-55 MIR4537 IGHV3-41 BTBD6 KIAA0125 IGHV4-31 IGHG1 IGHG3 IGHA2 IGHV1-69 IGHM NUDT14 LOC107987211 C14orf80 IGH IGHD PACS2 IGHG4 ELK2AP LOC105370697 MIR4539 TEX22 IGHV3-71 IGHV3-30 LINC00221 LINC00226 MIR8071-1 CRIP2

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          More Information


          Set Membership:

          Intragenic 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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