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          • Home
          • › Search Tool
          • › Search Results
          • › Hs02935808_cn
          See other RAD51C CNV Assays ›
          Gene Symbol
          RAD51C
          Assay Reference Genome
          Location

          Chr.17:58695082 on build GRCh38
          Cytoband
          17q22
          Assay ID Hs02935808_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:

          5889

          Gene Name:

          RAD51 paralog C

          Gene Aliases:

          BROVCA3, FANCO, R51H3, RAD51L2

          Location:

          Chr.17:58692538-58734342 on Build GRCh38

          Assay Gene Location:

          Within Exon 4
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          RAD51C NM_002876.3 2 368 NP_002867.1
          NM_058216.2 2 368 NP_478123.1
          NR_103872.1 2 368
          NR_103873.1 2 265
          XM_006722001.3 2 339 XP_006722064.1
          XM_006722002.3 2 339 XP_006722065.1
          XM_006722004.3 2 261 XP_006722067.1
          XM_006722005.3 2 247 XP_006722068.1
          XM_011525092.2 2 467 XP_011523394.1
          XM_011525093.2 2 628 XP_011523395.1
          XM_011525094.2 2 316 XP_011523396.1
          XM_017024914.1 2 261 XP_016880403.1
          XM_017024915.1 2 613 XP_016880404.1
          XM_017024916.1 3 521 XP_016880405.1
          XM_017024917.1 2 246 XP_016880406.1
          XM_017024918.1 2 315 XP_016880407.1
          XM_017024919.1 2 628 XP_016880408.1
          AA304618.1 2 199
          AF029669.1 2 339 AAC39604.1
          AF029670.1 2 313 AAC39605.1
          AI424321.1 1 269
          AK290487.1 2 339
          AK303363.1 2 278
          BC093930.1 2 334 AAH93930.1
          BC101485.1 2 334 AAI01486.1
          BC107753.1 2 372 AAI07754.1
          BM987503.1 1 272
          BT007339.1 2 297 AAP36003.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv833498 Chr.17:58652063 - 58815031 on Build GRCh38 Loss PPM1E RAD51C TEX14
          nsv1066945 Chr.17:58650965 - 58704810 on Build GRCh38 Loss RAD51C TEX14
          nsv428347 Chr.17:58565015 - 58717588 on Build GRCh38 Gain RAD51C TEX14

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          More Information


          Set Membership:

          Intragenic Exonic DGV Variation

          Panther Classification:

          Molecular Function -

          DNA metabolism protein nucleic acid metabolism protein

          Gene Ontology Categories:

          Function(s) Process(es)

          telomere maintenance via recombination
          double-strand break repair via homologous recombination
          DNA recombinase assembly
          DNA synthesis involved in DNA repair
          strand displacement
          DNA repair
          DNA recombination
          mitotic recombination
          sister chromatid cohesion
          female meiosis sister chromatid cohesion
          reciprocal meiotic recombination
          male meiosis I
          spermatogenesis
          blood coagulation
          response to ionizing radiation
          positive regulation of G2/M transition of mitotic cell cycle
          strand invasion
          chromosome organization involved in meiotic cell cycle
          recombinase activity
          four-way junction DNA binding
          DNA binding
          double-stranded DNA binding
          single-stranded DNA binding
          protein binding
          ATP binding
          DNA-dependent ATPase activity
          crossover junction endodeoxyribonuclease activity

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