Assay Details
Target Gene Details
Entrez Gene ID: | 54620 |
Gene Name: | F-box and leucine rich repeat protein 19 |
Gene Aliases: |
CXXC11, Fbl19, JHDM1C |
Location: |
Chr.16:30923055-30948783 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 6 - Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FBXL19 | NM_001099784.2 | NP_001093254.2 | ||
| NM_001282351.1 | NP_001269280.1 | |||
| AK098777.1 | BAC05410.1 | |||
| AK127701.1 | ||||
| AK302669.1 | ||||
| BC059173.1 | AAH59173.1 | |||
| CX781342.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv457483 | Chr.16:30892358 - 31180161 on Build GRCh38 | Loss |
|
| dgv35n68 | Chr.16:30833730 - 31036730 on Build GRCh38 | Loss |
|
| nsv953802 | Chr.16:30876680 - 30999279 on Build GRCh38 | Deletion |
|
| nsv833189 | Chr.16:30808387 - 30949474 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs140893916] 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