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          • Home
          • › Search Tool
          • › Search Results
          • › Hs03345696_cn
          See other SYF2 CNV Assays ›
          Gene Symbol
          SYF2
          Assay Reference Genome
          Location

          Chr.1:25229383 on build GRCh38
          Cytoband
          1p36.11
          Assay ID Hs03345696_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:

          25949

          Gene Name:

          SYF2 pre-mRNA splicing factor

          Gene Aliases:

          CBPIN, NTC31, P29, fSAP29

          Location:

          Chr.1:25222276-25232522 on Build GRCh38

          Assay Gene Location:

          Within Intron 2
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          SYF2 NM_015484.4 NP_056299.1
          NM_207170.3 NP_997053.1
          AF273089.1 AAG42073.1
          AK303582.1
          AK314859.1
          AL080166.1 CAB45754.1
          BC010862.1 AAH10862.1
          BG390792.1
          BI668848.1
          CV806249.1
          DR155437.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          dgv132n100 Chr.1:24981181 - 25393108 on Build GRCh38 Gain TMEM50A RSRP1 RHD RHCE SYF2 MIR4425
          esv3576582 Chr.1:24981195 - 25361084 on Build GRCh38 Gain TMEM50A RSRP1 RHD SYF2 MIR4425
          nsv7187 Chr.1:25197127 - 25229506 on Build GRCh38 Insertion SYF2
          nsv1160388 Chr.1:25177805 - 25266637 on Build GRCh38 Duplication RSRP1 SYF2
          dgv133n100 Chr.1:25228018 - 25361785 on Build GRCh38 Gain TMEM50A RSRP1 RHD SYF2

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Gene Ontology Categories:

          Function(s) Process(es)

          mRNA splicing, via spliceosome
          in utero embryonic development
          mitotic G2 DNA damage checkpoint
          gastrulation
          positive regulation of cell proliferation
          embryonic organ development
          protein binding
          poly(A) RNA binding

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          Host server : magellan-search-green-b49b87d85-9fm2r:80/100.66.79.29:80.
          git-commit: 5b8c860b7cdb41e9cfe07630520f6b51e109d38e
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