Assay Details
Target Gene Details
Entrez Gene ID: | 9871 |
Gene Name: | SEC24 homolog D, COPII coat complex component |
Gene Aliases: |
CLCRP2 |
Location: |
Chr.4:118722823-118838683 on Build GRCh38 |
Assay Gene Location: | Within Exon 25 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SEC24D | NM_001318066.1 | 23 | 3623 | NP_001304995.1 |
| NM_014822.3 | 23 | 3620 | NP_055637.2 | |
| XM_005263379.2 | 23 | 3497 | XP_005263436.1 | |
| XM_017008875.1 | 18 | 2778 | XP_016864364.1 | |
| AB018298.1 | 23 | 3523 | ||
| AK001390.1 | 20 | 2991 | ||
| AK125962.1 | 18 | 3455 | ||
| AK291765.1 | ||||
| AK309960.1 | 16 | 2359 | ||
| BC035761.1 | 23 | 3545 | AAH35761.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2759279 | Chr.4:117557693 - 118753587 on Build GRCh38 | Gain |
|
| nsv519017 | Chr.4:117907652 - 118850326 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79586191] 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