Genomic Map
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Target Gene Details
Entrez Gene ID: | 7026 |
Gene Name: | nuclear receptor subfamily 2 group F member 2 |
Gene Aliases: |
ARP1, CHTD4, COUPTFB, COUPTFII, NF-E3, NR2F1, SVP40, TFCOUP2 |
Location: |
Chr.15:96325928-96340263 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NR2F2 | NM_001145155.1 | 3 | 1198 | NP_001138627.1 |
| NM_001145156.1 | 3 | 830 | NP_001138628.1 | |
| NM_001145157.1 | 3 | 1291 | NP_001138629.1 | |
| NM_021005.3 | 3 | 2439 | NP_066285.1 | |
| AB307711.1 | ||||
| AK298824.1 | 3 | 878 | ||
| AK301595.1 | 3 | 835 | ||
| AK316086.1 | 3 | 830 | ||
| BC014664.1 | 3 | 1365 | AAH14664.1 | |
| BC042897.1 | 4 | 1796 | AAH42897.1 | |
| BC106083.1 | 3 | 1198 | AAI06084.1 | |
| BX538114.1 | ||||
| FM208183.1 | 3 | 1188 | ||
| HQ692848.1 | ||||
| HQ692849.1 | ||||
| HQ692850.1 | ||||
| M64497.1 | 3 | 1557 | AAA86429.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1141674 | Chr.15:95302056 - 96435607 on Build GRCh38 | Deletion |
 LINC00924
NR2F2
NR2F2-AS1
MIR1469
LINC01197
|
| dgv448n67 | Chr.15:96307811 - 96377491 on Build GRCh38 | Gain |
NR2F2
NR2F2-AS1
MIR1469
|
| nsv827449 | Chr.15:96323551 - 96342897 on Build GRCh38 | Gain |
NR2F2
NR2F2-AS1
MIR1469
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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