Assay Details
Target Gene Details
Entrez Gene ID: | 283551 |
Gene Name: | long intergenic non-protein coding RNA 1588 |
Gene Aliases: |
C14orf182 |
Location: |
Chr.14:49981669-50007520 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LINC01588 | NR_126496.1 | |||
NR_126497.1 | ||||
NR_126498.1 | ||||
AK090420.1 | BAC03401.1 | |||
AK091232.1 | ||||
BC128083.1 | ||||
BC144351.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1270 | Chr.14:49966729 - 49998159 on Build GRCh38 | Insertion | LINC01588 |
esv28926 | Chr.14:49426970 - 50475809 on Build GRCh38 | Gain+Loss | MIR4504 L2HGDH LINC01588 MAP4K5 LINC01599 RN7SL2 NEMF KLHDC1 SOS2 ATP5S POLE2 LOC100288910 KLHDC2 ARF6 LOC100506446 RPS29 RN7SL1 CDKL1 MGAT2 MIR6076 RPL36AL LRR1 DNAAF2 VCPKMT |
More Information
Additional Information:
For this assay, SNP(s) [rs113943852] 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: |
Intragenic Intronic Non-exonic DGV Variation |