Assay Details
Target Gene Details
Entrez Gene ID: | 114299 |
Gene Name: | paralemmin 2 |
Gene Aliases: |
AKAP2 |
Location: |
Chr.9:109640788-109951476 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALM2 | NM_001037293.2 | NP_001032370.1 | ||
| AK095003.1 | BAC04472.1 | |||
| BC039306.1 | AAH39306.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2670341 | Chr.9:109667920 - 109668235 on Build GRCh38 | Deletion |
|
| esv2610332 | Chr.9:109667923 - 109668237 on Build GRCh38 | Deletion |
|
| esv4643 | Chr.9:109667877 - 109668328 on Build GRCh38 | Loss |
|
| esv3545291 | Chr.9:109667913 - 109668290 on Build GRCh38 | Deletion |
|
| nsv957747 | Chr.9:109667928 - 109668224 on Build GRCh38 | Deletion |
|
| esv2738914 | Chr.9:109667909 - 109668237 on Build GRCh38 | Deletion |
|
| nsv831686 | Chr.9:109599537 - 109770842 on Build GRCh38 | Gain |
|
| esv9371 | Chr.9:109667781 - 109668434 on Build GRCh38 | Loss |
|
| esv2563678 | Chr.9:109667126 - 109668657 on Build GRCh38 | Deletion |
|
| esv1922439 | Chr.9:109667743 - 109668425 on Build GRCh38 | Deletion |
|
| nsv6661 | Chr.9:109652973 - 109678901 on Build GRCh38 | Insertion |
|
More Information
Set Membership: |
|

Genomic Map