Assay Details
Target Gene Details
Entrez Gene ID: | 285025 |
Gene Name: | coiled-coil domain containing 141 |
Gene Aliases: |
CAMDI |
Location: |
Chr.2:178825308-179050134 on Build GRCh38 |
Assay Gene Location: | Within Exon 26 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CCDC141 | XM_011510992.2 | 26 | 5931 | XP_011509294.1 |
| XM_011510993.2 | 25 | 5839 | XP_011509295.1 | |
| XM_017003867.1 | 26 | 6016 | XP_016859356.1 | |
| XM_017003868.1 | 25 | 5801 | XP_016859357.1 | |
| XM_017003869.1 | 25 | 5712 | XP_016859358.1 | |
| XM_017003870.1 | 20 | 4841 | XP_016859359.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834470 | Chr.2:178690425 - 178863999 on Build GRCh38 | Gain |
|
| esv3593495 | Chr.2:178809374 - 178845060 on Build GRCh38 | Gain |
|
| esv3593496 | Chr.2:178820157 - 178969265 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114009751,rs73040354] 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