Assay Details
Target Gene Details
Entrez Gene ID: | 90459 |
Gene Name: | exoribonuclease 1 |
Gene Aliases: |
3'HEXO, HEXO, THEX1 |
Location: |
Chr.8:8892225-9100262 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ERI1 | XM_017013949.1 | XP_016869438.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv972228 | Chr.8:8895187 - 8901517 on Build GRCh38 | Deletion | ERI1 |
nsv610190 | Chr.8:8886730 - 8909371 on Build GRCh38 | Loss | MFHAS1 ERI1 |
nsv831228 | Chr.8:8750877 - 8933280 on Build GRCh38 | Loss | MFHAS1 ERI1 |
dgv1370e214 | Chr.8:8851973 - 8899115 on Build GRCh38 | Gain | MFHAS1 ERI1 |
nsv831229 | Chr.8:8894013 - 9068725 on Build GRCh38 | Gain+Loss | MIR4660 ERI1 |
nsv1018828 | Chr.8:8752370 - 8933150 on Build GRCh38 | Loss | MFHAS1 ERI1 |
More Information
Additional Information:
For this assay, SNP(s) [rs75465272] 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 |