Product Details

Assay Reference Genome
Location

Chr.2:27364761 on build GRCh38
Cytoband
2p23.3
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs78914478] 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.

Target Gene Details

Entrez Gene ID
8890
Gene Symbol
EIF2B4
Gene Name
eukaryotic translation initiation factor 2B subunit delta
Gene Aliases
EIF-2B, EIF2B, EIF2Bdelta
Location
Chr.2:27364352-27370457 on build GRCh38
Assay Gene Location
Overlaps Intron 12 - Exon 12
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
EIF2B4 NM_001034116.1 NP_001029288.1
NM_001318965.1 NP_001305894.1
NM_001318966.1 NP_001305895.1
NM_001318967.1 NP_001305896.1
NM_001318968.1 NP_001305897.1
NM_001318969.1 NP_001305898.1
NM_015636.3 NP_056451.3
NM_172195.3 NP_751945.2
XM_006712132.1 XP_006712195.1
XM_011533147.2 XP_011531449.1
AF057699.1 AAQ13438.1
AF086520.1
AF112207.1 AAF17195.1
AF218009.1 AAG17251.1
AJ011305.1 CAB57260.1
AJ011306.1 CAB57261.1
AL050109.1 CAB43277.1
BC001870.1 AAH01870.1
BC091502.1 AAH91502.1
JQ991007.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv833614 Chr2:27263559 - 27452213 on Build GRCh38 Gain LOC105374363 EIF2B4 ZNF513 UCN GTF3C2-AS1 SNX17 FTH1P3 DNAJC5G SLC30A3 MPV17 IFT172 TRIM54 PPM1G KRTCAP3 NRBP1 GTF3C2
esv3575209 Chr2:27334578 - 27389381 on Build GRCh38 Gain GTF3C2-AS1 SNX17 LOC105374363 EIF2B4 ZNF513 PPM1G GTF3C2
nsv581244 Chr2:27335385 - 27480628 on Build GRCh38 Loss GTF3C2-AS1 SNX17 FTH1P3 LOC105374363 EIF2B4 ZNF513 IFT172 PPM1G KRTCAP3 NRBP1 GTF3C2

View Full Product Details