Assay Details
Target Gene Details
Entrez Gene ID: | 89887 |
Gene Name: | zinc finger protein 628 |
Gene Aliases: |
ZEC, Zfp628 |
Location: |
Chr.19:55476332-55484487 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZNF628 | NM_033113.2 | 3 | 2728 | NP_149104.3 |
XM_005259371.3 | 2 | 2373 | XP_005259428.1 | |
BC089449.1 | 3 | 2728 | AAH89449.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv2552 | Chr.19:55467079 - 55498718 on Build GRCh38 | Insertion | SSC5D ZNF628 NAT14 |
nsv580343 | Chr.19:55466542 - 55521721 on Build GRCh38 | Loss | SSC5D ZNF628 NAT14 |
nsv953624 | Chr.19:55302033 - 55625034 on Build GRCh38 | Deletion | ISOC2 MIR6805 SBK2 ZNF524 FAM71E2 SHISA7 TMEM238 SBK3 BRSK1 NAT14 COX6B2 TMEM150B IL11 ZNF865 SSC5D RPL28 ZNF579 ZNF784 TMEM190 ZNF628 KMT5C UBE2S FIZ1 |
More Information
Additional Information:
For this assay, SNP(s) [rs114775834] 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 |