Assay Details
Target Gene Details
Entrez Gene ID: | 284119 |
Gene Name: | polymerase I and transcript release factor |
Gene Aliases: |
CAVIN, CAVIN1, CGL4, FKSG13, cavin-1 |
Location: |
Chr.17:42402449-42423320 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PTRF | NM_012232.5 | 2 | 2059 | NP_036364.2 |
| AF312393.1 | 2 | 2256 | AAG27093.1 | |
| AK000715.1 | 2 | 1545 | ||
| AK092406.1 | 4 | 1698 | ||
| BC004295.1 | 1 | 1269 | AAH04295.1 | |
| BC008849.1 | 2 | 1342 | AAH08849.1 | |
| BC066123.1 | 2 | 1995 | AAH66123.1 | |
| BC073759.1 | 2 | 1881 | AAH73759.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv470586 | Chr.17:42362183 - 42459270 on Build GRCh38 | Gain |
|
| nsv833449 | Chr.17:42274854 - 42421081 on Build GRCh38 | Loss |
|
| nsv575051 | Chr.17:42317580 - 42498404 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79683345] 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