Assay Details
Target Gene Details
Entrez Gene ID: | 84922 |
Gene Name: | FLT3 interacting zinc finger 1 |
Gene Aliases: |
ZNF798 |
Location: |
Chr.19:55591371-55599703 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FIZ1 | NM_032836.2 | NP_116225.2 | ||
XM_005259352.4 | 1 | 725 | XP_005259409.1 | |
XM_011527426.2 | XP_011525728.1 | |||
AK027674.1 | BAB55286.1 | |||
AK160385.1 | 1 | 3122 | BAD18728.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv953624 | Chr.19:55302033 - 55625034 on Build GRCh38 | Deletion | TMEM150B TMEM190 SSC5D IL11 ZNF628 RPL28 FIZ1 TMEM238 FAM71E2 SBK2 ZNF865 ISOC2 ZNF579 SBK3 SHISA7 BRSK1 KMT5C MIR6805 ZNF784 COX6B2 UBE2S ZNF524 NAT14 |
nsv828643 | Chr.19:55547914 - 55643457 on Build GRCh38 | Loss | ZNF865 ZNF579 FIZ1 ZNF784 ZNF524 LOC107983998 ZNF581 ZNF580 |
More Information
Additional Information:
For this assay, SNP(s) [rs111957536] 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 |