Genomic Map
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Target Gene Details
Entrez Gene ID: | 1938 |
Gene Name: | eukaryotic translation elongation factor 2 |
Gene Aliases: |
EEF-2, EF-2, EF2, SCA26 |
Location: |
Chr.19:3976056-3985463 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EEF2 | NM_001961.3 | 15 | 2914 | NP_001952.1 |
| AK298498.1 | ||||
| AK299225.1 | ||||
| BC024689.1 | 8 | 1809 | AAH24689.1 | |
| BC126259.1 | ||||
| BC136313.1 | ||||
| M19997.1 | 6 | 1333 | AAA50388.1 | |
| X51466.1 | 14 | 2831 | CAA35829.1 | |
| Z11692.1 | 14 | 2831 | CAA77750.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833715 | Chr.19:3786758 - 3977144 on Build GRCh38 | Loss |
 ZFR2
NMRK2
EEF2
DAPK3
MIR637
ATCAY
MATK
|
| nsv953949 | Chr.19:3959703 - 4089602 on Build GRCh38 | Deletion |
PIAS4
ZBTB7A
SNORD37
EEF2
DAPK3
MIR637
|
| esv1001715 | Chr.19:3972105 - 3981537 on Build GRCh38 | Deletion |
EEF2
|
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Additional Information:
For this assay, SNP(s) [rs73530391] 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
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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