Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 2120 |
Gene Name: | ETS variant 6 |
Gene Aliases: |
TEL, TEL/ABL, THC5 |
Location: |
Chr.12:11649601-11895402 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ETV6 | NM_001987.4 | NP_001978.1 | ||
| XM_011520607.2 | XP_011518909.1 | |||
| XM_011520611.2 | XP_011518913.1 | |||
| XM_017018990.1 | XP_016874479.1 | |||
| XM_017018991.1 | XP_016874480.1 | |||
| AK289441.1 | ||||
| BC043399.1 | AAH43399.1 | |||
| FR719953.1 | ||||
| KU178049.1 | ||||
| KU178050.1 | ||||
| U11732.1 | AAA19786.1 | |||
| Z35761.1 | CAA84815.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv951328 | Chr.12:11650867 - 11656766 on Build GRCh38 | Duplication |
 ETV6
|
| nsv609 | Chr.12:11651252 - 11686040 on Build GRCh38 | Insertion |
ETV6
|
| nsv1046355 | Chr.12:11501836 - 12890185 on Build GRCh38 | Loss |
RPL13AP20
MANSC1
APOLD1
LOH12CR2
MIR1244-4
BORCS5
LOC105369662
CREBL2
ETV6
MIR613
LOC100506248
GPR19
LRP6
DDX47
DUSP16
LINC01252
CDKN1B
BCL2L14
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs74062342] 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
|
Panther Classification:
Gene Ontology Categories:
Back To Top