Assay Details
Target Gene Details
Entrez Gene ID: | 440503 |
Gene Name: | perilipin 5 |
Gene Aliases: |
LSDA5, LSDP5, MLDP, OXPAT |
Location: |
Chr.19:4522531-4535196 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PLIN5 | NM_001013706.2 | NP_001013728.2 | ||
BC131524.1 | ||||
DQ839131.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833720 | Chr.19:4367721 - 4540556 on Build GRCh38 | Loss | LRG1 UBXN6 PLIN4 SH3GL1 HDGFRP2 MIR4746 PLIN5 CHAF1A |
nsv578444 | Chr.19:4502189 - 4559634 on Build GRCh38 | Gain | LRG1 SEMA6B PLIN4 HDGFRP2 PLIN5 |
nsv428361 | Chr.19:4510042 - 4689189 on Build GRCh38 | Loss | LRG1 TNFAIP8L1 SEMA6B PLIN4 DPP9-AS1 MYDGF DPP9 PLIN5 |
More Information
Additional Information:
For this assay, SNP(s) [rs76930576] 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 |