Assay Details
Target Gene Details
Entrez Gene ID: | 6397 |
Gene Name: | SEC14 like lipid binding 1 |
Gene Aliases: |
PRELID4A, SEC14L |
Location: |
Chr.17:77088643-77217101 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SEC14L1 | NM_001204408.1 | NP_001191337.1 | ||
| NM_001204410.1 | NP_001191339.1 | |||
| FM995495.1 | ||||
| FM995496.1 | ||||
| FM995497.1 | ||||
| FM995498.1 | ||||
| FN357114.1 | ||||
| FN357120.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv5784n54 | Chr.17:77049144 - 77101828 on Build GRCh38 | Gain |
|
| esv3641304 | Chr.17:77065524 - 77180984 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76088609] 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