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          • Home
          • › Search Tool
          • › Search Results
          • › Hs03358638_cn
          See other SYF2 CNV Assays ›
          Gene Symbol
          SYF2
          Assay Reference Genome
          Location

          Chr.1:25231555 on build GRCh38
          Cytoband
          Assay ID Hs03358638_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:

          25949

          Gene Name:

          SYF2 pre-mRNA splicing factor

          Gene Aliases:

          CBPIN, NTC31, P29, fSAP29

          Location:

          Chr.1:25222276-25232502 on Build GRCh38

          Assay Gene Location:

          Within Intron 2
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          SYF2 NM_015484.5 NP_056299.1
          NM_207170.4 NP_997053.1
          AF273089.1 AAG42073.1
          AK303582.1 BAG64600.1
          AK314859.1 BAG37375.1
          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: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv6321813 Chr.1:25173901 - 25405600 on Build GRCh38 Duplication TMEM50A RHCE SYF2 RHD RSRP1
          dgv132n100 Chr.1:24981181 - 25393108 on Build GRCh38 Gain TMEM50A RHCE MIR4425 SYF2 RHD RSRP1
          esv3576582 Chr.1:24981195 - 25361084 on Build GRCh38 Gain TMEM50A MIR4425 SYF2 RHD RSRP1
          nsv6319333 Chr.1:25223901 - 25361200 on Build GRCh38 Duplication TMEM50A SYF2 RHD RSRP1
          nsv1160388 Chr.1:25177805 - 25266637 on Build GRCh38 Duplication SYF2 RSRP1
          dgv133n100 Chr.1:25228018 - 25361785 on Build GRCh38 Gain TMEM50A SYF2 RHD RSRP1

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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
          mRNA processing
          mitotic G2 DNA damage checkpoint
          gastrulation
          positive regulation of cell proliferation
          RNA splicing
          embryonic organ development
          RNA binding
          protein binding

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