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          • Home
          • › Search Tool
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          • › Hs06971509_cn
          See other EIF4B CNV Assays ›
          Gene Symbol
          EIF4B
          Assay Reference Genome
          Location

          Chr.12:53039430 on build GRCh38
          Cytoband
          12q13.13
          Assay ID Hs06971509_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price 4,505.00
          Your Price
          Online offer:
          4505.0
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          1975

          Gene Name:

          eukaryotic translation initiation factor 4B

          Gene Aliases:

          EIF-4B, PRO1843

          Location:

          Chr.12:53006258-53042209 on Build GRCh38

          Assay Gene Location:

          Within Intron 13
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          EIF4B NM_001300821.1 NP_001287750.1
          NM_001417.5 NP_001408.2
          AB076839.1 BAB82380.1
          AK092188.1
          AK222528.1 BAD96248.1
          AK293731.1
          AK299329.1
          AK299510.1
          AK299526.1
          AK307496.1
          BC001097.1 AAH01097.1
          BC073139.1 AAH73139.1
          BC073154.1 AAH73154.1
          BC098437.1 AAH98437.1
          BP243230.1
          CR456958.1 CAG33239.1
          CR627377.1 CAH10474.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv517066 Chr.12:53006394 - 53340722 on Build GRCh38 Loss MFSD5 TNS2 PFDN5 ESPL1 SOAT2 ITGB7 SPRYD3 SP7 CSAD ZNF740 IGFBP6 EIF4B AAAS C12orf10 LOC283335 RARG MIR6757

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          More Information


          Additional Information:

          For this assay, SNP(s) [rs140983860] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Panther Classification:

          Molecular Function -

          translation initiation factor

          Gene Ontology Categories:

          Function(s) Process(es)

          nuclear-transcribed mRNA poly(A) tail shortening
          formation of translation preinitiation complex
          cytoplasmic translation
          translational initiation
          regulation of translational initiation
          eukaryotic translation initiation factor 4F complex assembly
          nucleotide binding
          RNA binding
          translation initiation factor activity
          helicase activity
          protein binding
          RNA strand annealing activity
          RNA strand-exchange activity
          ribosomal small subunit binding
          poly(A) RNA binding

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