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          • Home
          • › Search Tool
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          • › Hs00963891_cn
          See other ADAMTS13 CNV Assays ›
          Gene Symbol
          ADAMTS13
          Assay Reference Genome
          Location

          Chr.9:133459174 on build GRCh38
          Cytoband
          Assay ID Hs00963891_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:

          11093

          Gene Name:

          ADAM metallopeptidase with thrombospondin type 1 motif 13

          Gene Aliases:

          ADAM-TS13, ADAMTS-13, C9orf8, VWFCP, vWF-CP

          Location:

          Chr.9:240431-285480 on Build GRCh38

          Assay Gene Location:

          Within Exon 32
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          ADAMTS13 NM_139025.5 29 4355 NP_620594.1
          NM_139026.6 29 4094 NP_620595.1
          NM_139027.6 29 4187 NP_620596.2
          NR_024514.3 18 2762
          XM_011518176.4 22 4431 XP_011516478.1
          XM_011518178.3 19 3048 XP_011516480.1
          XM_011518179.1 19 3091 XP_011516481.1
          XM_017014232.2 29 4982 XP_016869721.1
          XM_017014233.2 29 4364 XP_016869722.1
          XM_017014234.2 23 3522 XP_016869723.1
          XM_047422699.1 29 4262 XP_047278655.1
          AB069698.2 29 4722 BAB69487.2
          AJ305314.1 29 4137 CAC83682.1
          AJ420810.1 29 4230 CAD12729.1
          AK124983.1 7 1299 BAG54119.1
          AL136809.1 5 862 CAB66743.1
          AV655072.1 2 305
          AY055376.1 29 4386 AAL17652.1
          AY358118.1 22 3490 AAQ88485.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv2739138 Chr.9:132727483 - 135521553 on Build GRCh38 Deletion TSC1 MIR548AW GFI1B LOC124902325 SNORD141A BRD3 RPL7A CACFD1 MIR3689D1 REXO4 SNORD36A LOC101928525 FCN2 FCN1 PIERCE1 SNORD36B RNU6ATAC SARDH LOC101448202 ADAMTSL2 LOC105376306 ABO WDR5 LOC401557 LINC02247 PPP1R26-AS1 FAM163B VAV2 SNORD24 MIR3689C GTF3C5 MIR3689B MIR4669 ADAMTS13 LCN1 SNORD36C MIR3689D2 SURF4 MIR3689A PPP1R26 LOC100506532 RALGDS COL5A1 LOC100130548 WDR5-DT CELP STKLD1 OLFM1 MIR6877 DBH-AS1 MYMK RXRA DBH SLC2A6 MRPS2 AK8 MIR3689F SURF2 SPACA9 LOC105376314 OBP2B BRD3OS GBGT1 SURF6 COL5A1-AS1 CEL SURF1 MIR3689E LINC02907 MED22

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          More Information


          Set Membership:

          Intragenic Exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          proteolysis
          cell-matrix adhesion
          integrin-mediated signaling pathway
          blood coagulation
          hemostasis
          glycoprotein metabolic process
          response to toxic substance
          response to amine
          protein processing
          protein catabolic process
          platelet activation
          extracellular matrix organization
          response to interferon-gamma
          response to tumor necrosis factor
          response to potassium ion
          peptide catabolic process
          response to interleukin-4
          cellular response to lipopolysaccharide
          cellular response to interferon-gamma
          cellular response to interleukin-4
          cellular response to tumor necrosis factor
          endopeptidase activity
          metalloendopeptidase activity
          integrin binding
          calcium ion binding
          protein binding
          peptidase activity
          metallopeptidase activity
          zinc ion binding
          hydrolase activity
          metal ion binding

          Back To Top

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