Hs07186495_cn

• Gene Symbol: PFDN4
• Assay Reference Genome Location: Chr.20:54208473 on build GRCh38
• Cytoband: 20q13.2

Target Gene Details

• Entrez Gene ID: 5203
• Gene Name: prefoldin subunit 4
• Gene Aliases: C1, PFD4
• Location: Chr.20:54207963-54219953 on Build GRCh38
• Assay Gene Location: Overlaps Intron 1 - Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PFDN4	NM_002623.3			NP_002614.2
	XM_017027879.1			XP_016883368.1
	AK312059.1
	BC010953.1			AAH10953.1
	CN482830.1
	U41816.1			AAB17063.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv586224	Chr.20:53858311 - 54662951 on Build GRCh38	Gain	DOK5 SUMO1P1 MIR4756 BCAS1 CYP24A1 PFDN4
nsv834010	Chr.20:54143285 - 54316400 on Build GRCh38	Loss	CYP24A1 PFDN4

More Information

Additional Information:

For this assay, SNP(s) [rs137871814] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

protein folding

Function(s)

protein binding
unfolded protein binding
chaperone binding