Hs02930746_cn

• Gene Symbol: PRND
• Assay Reference Genome Location: Chr.20:4728148 on build GRCh38
• Cytoband: 20p13

Target Gene Details

• Entrez Gene ID: 23627
• Gene Name: prion protein 2 (dublet)
• Gene Aliases: DOPPEL, DPL, PrPLP, dJ1068H6.4
• Location: Chr.20:4721854-4728462 on Build GRCh38
• Assay Gene Location: Within Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PRND	NM_012409.3	2	3724	NP_036541.2
	AF086354.1	1	254
	BC043644.2	2	3668	AAH43644.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv3645074	Chr.20:4205961 - 5037636 on Build GRCh38	Gain	RASSF2 ADRA1D SLC23A2 PRNP PRNT PRND
nsv179053	Chr.20:4727804 - 4730313 on Build GRCh38	Deletion	PRND
nsv585310	Chr.20:4586645 - 4794039 on Build GRCh38	Gain	RASSF2 PRNP PRNT PRND

More Information

Additional Information:

For this assay, SNP(s) [rs144848773] 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, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

cellular copper ion homeostasis
protein homooligomerization

Function(s)

copper ion binding