Assay Details
Target Gene Details
Entrez Gene ID: | 79726 |
Gene Name: | WD repeat domain 59 |
Gene Aliases: |
FP977 |
Location: |
Chr.16:74873568-74985146 on Build GRCh38 |
Assay Gene Location: | Within Intron 26 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WDR59 | NM_030581.3 | NP_085058.3 | ||
XM_005256146.3 | XP_005256203.1 | |||
XM_011523331.2 | XP_011521633.1 | |||
XM_011523332.2 | XP_011521634.1 | |||
XM_017023667.1 | XP_016879156.1 | |||
XM_017023668.1 | XP_016879157.1 | |||
XM_017023669.1 | XP_016879158.1 | |||
XM_017023670.1 | XP_016879159.1 | |||
AB067510.1 | BAB67816.1 | |||
AF370390.1 | AAQ15226.1 | |||
AK022332.1 | BAB14015.1 | |||
AK091316.1 | ||||
AL832078.1 | ||||
BC014887.2 | AAH14887.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833280 | Chr.16:74821913 - 75043329 on Build GRCh38 | Loss | ZNRF1 WDR59 |
dgv3019n100 | Chr.16:74834429 - 74955590 on Build GRCh38 | Loss | WDR59 |
nsv572978 | Chr.16:74839676 - 74956106 on Build GRCh38 | Loss | WDR59 |
nsv572977 | Chr.16:74839615 - 74920999 on Build GRCh38 | Loss | WDR59 |
More Information
Additional Information:
For this assay, SNP(s) [rs113406680] 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 |