Assay Details
Target Gene Details
Entrez Gene ID: | 1982 |
Gene Name: | eukaryotic translation initiation factor 4 gamma 2 |
Gene Aliases: |
AAG1, DAP5, NAT1, P97 |
Location: |
Chr.11:10797046-10809035 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 20 - Exon 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
EIF4G2 | NM_001042559.2 | NP_001036024.3 | ||
NM_001172705.1 | NP_001166176.1 | |||
NM_001418.3 | NP_001409.3 | |||
AB063323.1 | BAB93515.1 | |||
AB073654.1 | BAE45728.1 | |||
AB209267.1 | BAD92504.1 | |||
AK223548.1 | BAD97268.1 | |||
AK302886.1 | ||||
AY513274.1 | AAT08027.1 | |||
BC014930.2 | AAH14930.2 | |||
BC018746.1 | ||||
BC018975.2 | ||||
BC039851.1 | AAH39851.1 | |||
BC043149.1 | ||||
BC065276.1 | ||||
BC111415.1 | ||||
BC111548.1 | ||||
BX647799.1 | ||||
U73824.1 | AAB49973.1 | |||
U76111.1 | AAC51166.1 | |||
X89713.1 | CAA61857.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv483000 | Chr.11:10678454 - 12678453 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs200629956] 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: |
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Panther Classification:
Gene Ontology Categories:
