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See other EIF4G3 CNV Assays ›
Gene Symbol
EIF4G3
Assay Reference Genome
Location

Chr.1:20806639 on build GRCh38
Cytoband
1p36.12
Assay ID Hs00837414_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:

8672

Gene Name:

eukaryotic translation initiation factor 4 gamma 3

Gene Aliases:

eIF-4G 3, eIF4G 3, eIF4GII

Location:

Chr.1:20806292-21177320 on Build GRCh38

Assay Gene Location:

Within Exon 43
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
EIF4G3 NM_001198801.1 35 6168 NP_001185730.1
NM_001198802.1 35 6078 NP_001185731.1
NM_003760.4 32 5694 NP_003751.2
XM_011542356.2 38 6768 XP_011540658.1
XM_011542361.2 37 6657 XP_011540663.1
XM_011542370.1 38 6771 XP_011540672.1
XM_011542371.1 36 6513 XP_011540673.1
XM_011542374.1 35 6480 XP_011540676.1
XM_011542375.2 35 8068 XP_011540677.1
XM_011542381.2 25 4154 XP_011540683.1
XM_017002672.1 39 8306 XP_016858161.1
XM_017002673.1 37 6750 XP_016858162.1
XM_017002674.1 37 6747 XP_016858163.1
XM_017002675.1 37 6738 XP_016858164.1
XM_017002676.1 36 6717 XP_016858165.1
XM_017002677.1 36 6594 XP_016858166.1
XM_017002678.1 37 6660 XP_016858167.1
XM_017002679.1 37 6657 XP_016858168.1
XM_017002680.1 34 5687 XP_016858169.1
XM_017002681.1 37 6654 XP_016858170.1
XM_017002682.1 36 6636 XP_016858171.1
XM_017002683.1 36 6636 XP_016858172.1
XM_017002684.1 37 8162 XP_016858173.1
XM_017002685.1 36 6627 XP_016858174.1
XM_017002686.1 36 6624 XP_016858175.1
XM_017002687.1 36 6624 XP_016858176.1
XM_017002688.1 33 5653 XP_016858177.1
XM_017002689.1 37 6624 XP_016858178.1
XM_017002690.1 36 6621 XP_016858179.1
XM_017002691.1 35 6606 XP_016858180.1
XM_017002692.1 35 6603 XP_016858181.1
XM_017002693.1 34 6474 XP_016858182.1
XM_017002694.1 36 6546 XP_016858183.1
XM_017002695.1 36 6543 XP_016858184.1
XM_017002696.1 35 6525 XP_016858185.1
XM_017002697.1 35 6522 XP_016858186.1
XM_017002698.1 35 6513 XP_016858187.1
XM_017002699.1 36 6513 XP_016858188.1
XM_017002700.1 34 6492 XP_016858189.1
XM_017002701.1 34 6489 XP_016858190.1
XM_017002702.1 34 6423 XP_016858191.1
XM_017002703.1 32 5584 XP_016858192.1
XM_017002704.1 36 6636 XP_016858193.1
XM_017002705.1 37 5931 XP_016858194.1
XM_017002706.1 36 5820 XP_016858195.1
XM_017002707.1 34 5763 XP_016858196.1
XM_017002708.1 33 5652 XP_016858197.1
XM_017002709.1 34 6368 XP_016858198.1
AB209119.1 35 6037 BAD92356.1
AF012072.2 32 5694 AAC02903.2
BC094683.1 AAH94683.1

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More Information


Additional Information:

For this assay, SNP(s) [rs532703823] 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 Exonic non-DGV Variation

Panther Classification:

Molecular Function -

translation factor translation initiation factor translational protein

Gene Ontology Categories:

Function(s) Process(es)

translational initiation
regulation of translational initiation
viral process
RNA cap binding
translation initiation factor activity
translation factor activity, RNA binding
poly(A) RNA binding

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