Assay Details
Target Gene Details
Entrez Gene ID: | 5204 |
Gene Name: | prefoldin subunit 5 |
Gene Aliases: |
MM-1, MM1, PFD5 |
Location: |
Chr.12:53295451-53299450 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PFDN5 | NM_002624.3 | NP_002615.2 | ||
NM_145897.2 | NP_665904.1 | |||
AB055803.1 | BAB32644.1 | |||
AB055804.1 | BAB32645.1 | |||
AB055805.1 | BAB32646.1 | |||
AK024094.1 | 3 | 695 | ||
AK292623.1 | ||||
BC062671.1 | AAH62671.1 | |||
BE392248.1 | ||||
BT007195.1 | AAP35859.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv517066 | Chr.12:53006394 - 53340722 on Build GRCh38 | Loss | ITGB7 EIF4B C12orf10 CSAD TNS2 ZNF740 LOC283335 RARG IGFBP6 SP7 ESPL1 PFDN5 MFSD5 SPRYD3 SOAT2 AAAS MIR6757 |
More Information
Additional Information:
For this assay, SNP(s) [rs149989496] 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 |