Assay Details
Target Gene Details
Entrez Gene ID: | 103021164 |
Gene Name: | cancer susceptibility candidate 21 (non-protein coding) |
Gene Aliases: |
CARLo-2, LINC01244 |
Location: |
Chr.8:127244637-127392631 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CASC21 | NR_117099.1 | |||
| AL709378.1 |
Target Gene Details
Entrez Gene ID: | 727677 |
Gene Name: | cancer susceptibility candidate 8 (non-protein coding) |
Gene Aliases: |
CARLo-1, LINC00860 |
Location: |
Chr.8:127289676-127482139 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CASC8 | NR_117100.1 | |||
| DQ515897.1 | ||||
| DQ515898.1 | ||||
| DQ515899.1 | ||||
| JX003864.1 | ||||
| JX003866.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv275357 | Chr.8:127320952 - 127321306 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72712310] 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