Assay Details
Target Gene Details
Entrez Gene ID: | 11217 |
Gene Name: | A-kinase anchoring protein 2 |
Gene Aliases: |
AKAP-2, AKAPKL, MISP2, PRKA2 |
Location: |
Chr.9:110048598-110172512 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| AKAP2 | NM_001004065.4 | NP_001004065.2 | ||
| NM_001198656.1 | NP_001185585.1 | |||
| AK057098.1 | ||||
| AK304311.1 | ||||
| BC146863.1 | ||||
| BC171800.1 | ||||
| BE674805.1 |
Target Gene Details
Entrez Gene ID: | 445815 |
Gene Name: | PALM2-AKAP2 readthrough |
Gene Aliases: |
AKAP2 |
Location: |
Chr.9:109780297-110172512 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALM2-AKAP2 | NM_007203.4 | NP_009134.1 | ||
| NM_147150.2 | NP_671492.1 | |||
| AB023137.1 | ||||
| AJ303079.1 | CAC38839.1 | |||
| AJ312217.1 | CAC59702.1 | |||
| BC140818.1 | ||||
| BX649126.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv494n21 | Chr.9:109952819 - 110202456 on Build GRCh38 | Gain |
|
| esv3573350 | Chr.9:110061538 - 110069597 on Build GRCh38 | Loss |
|
| nsv1150859 | Chr.9:110067907 - 110068654 on Build GRCh38 | Deletion |
|
| nsv466480 | Chr.9:110067939 - 110096621 on Build GRCh38 | Loss |
|
| esv28884 | Chr.9:110067919 - 110068852 on Build GRCh38 | Loss |
|
| esv3621448 | Chr.9:109954078 - 110129324 on Build GRCh38 | Gain |
|
| esv3621452 | Chr.9:110067914 - 110068620 on Build GRCh38 | Loss |
|
| nsv1043494 | Chr.9:109988131 - 110214627 on Build GRCh38 | Gain |
|
| nsv1117903 | Chr.9:110067915 - 110068618 on Build GRCh38 | Deletion |
|
| esv3621449 | Chr.9:109959589 - 110304023 on Build GRCh38 | Gain |
|
| esv2195369 | Chr.9:110067755 - 110068737 on Build GRCh38 | Deletion |
|
| esv2501710 | Chr.9:110067316 - 110068996 on Build GRCh38 | Deletion |
|
| nsv471314 | Chr.9:110059903 - 110093364 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs116415864] 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: |
|

Genomic Map