Assay Details
Target Gene Details
Entrez Gene ID: | 132864 |
Gene Name: | cytoplasmic polyadenylation element binding protein 2 |
Gene Aliases: |
CPE-BP2, CPEB-2, hCPEB-2 |
Location: |
Chr.4:15002451-15070153 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CPEB2 | NM_001177381.1 | 11 | 3858 | NP_001170852.1 |
| NM_001177382.1 | 12 | 3939 | NP_001170853.1 | |
| NM_001177383.1 | 11 | 3849 | NP_001170854.1 | |
| NM_001177384.1 | 10 | 3834 | NP_001170855.1 | |
| NM_182485.2 | 11 | 3915 | NP_872291.2 | |
| NM_182646.2 | 10 | 3825 | NP_872587.2 | |
| XM_005248135.3 | 12 | 4171 | XP_005248192.2 | |
| XM_011513777.2 | 11 | 4147 | XP_011512079.1 | |
| XM_017007733.1 | 12 | 2307 | XP_016863222.1 | |
| XM_017007734.1 | 12 | 2308 | XP_016863223.1 | |
| BC103939.1 | 12 | 2530 | ||
| BC103940.1 | 11 | 2653 | AAI03941.1 | |
| BC103941.1 | 11 | 2590 | AAI03942.1 | |
| BC103942.1 | 13 | 2611 | AAI03943.1 | |
| BC105925.1 | 10 | 2572 | AAI05926.1 | |
| BI857384.1 | 1 | 216 | ||
| BX640753.1 | 2 | 1092 | CAE45860.1 |
Target Gene Details
Entrez Gene ID: | 101929095 |
Gene Name: | uncharacterized LOC101929095 |
Gene Aliases: |
- |
Location: |
Chr.4:15004942-15427914 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC101929095 | NR_125911.1 | |||
| DB497821.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv829868 | Chr.4:14962935 - 15163082 on Build GRCh38 | Gain |
|
| nsv461280 | Chr.4:14960872 - 15079750 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs141127740] 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: |
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Genomic Map