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See other PLIN5 CNV Assays ›
Gene Symbol
PLIN5
Assay Reference Genome
Location

Chr.19:4528293 on build GRCh38
Cytoband
19p13.3
Assay ID Hs04019741_cn
Size
Availability Made To Order
Catalog # 4400291
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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 5
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 PLIN4 PLIN5 UBXN6 SH3GL1 CHAF1A LRG1 MIR4746 HDGFRP2
nsv578444 Chr.19:4502189 - 4559634 on Build GRCh38 Gain PLIN4 PLIN5 LRG1 HDGFRP2 SEMA6B
nsv428361 Chr.19:4510042 - 4689189 on Build GRCh38 Loss PLIN4 PLIN5 MYDGF DPP9 DPP9-AS1 LRG1 SEMA6B TNFAIP8L1

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More Information


Additional Information:

For this assay, SNP(s) [rs111956527] 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

Panther Classification:

Molecular Function -

scaffold/adaptor protein

Gene Ontology Categories:

Function(s) Process(es)


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