Assay Details
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: | Within Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PFDN4 | NM_002623.3 | 4 | 903 | NP_002614.2 |
XM_017027879.1 | 4 | 1187 | XP_016883368.1 | |
U41816.1 | 4 | 764 | 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 | BCAS1 SUMO1P1 DOK5 CYP24A1 PFDN4 MIR4756 |
nsv834010 | Chr.20:54143285 - 54316400 on Build GRCh38 | Loss | CYP24A1 PFDN4 |
More Information
Additional Information:
For this assay, SNP(s) [rs150624897] 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 |