Hs01933389_cn

• Gene Symbol: ZNF708
• Assay Reference Genome Location: Chr.19:21293039 on build GRCh38
• Cytoband: 19p12

Target Gene Details

• Entrez Gene ID: 7562
• Gene Name: zinc finger protein 708
• Gene Aliases: KOX8, ZNF15, ZNF15L1
• Location: Chr.19:21290388-21329439 on Build GRCh38
• Assay Gene Location: Within Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ZNF708	NM_001297560.1	4	2209	NP_001284489.1
	NM_001297561.1	3	2000	NP_001284490.1
	NM_021269.2	4	2125	NP_067092.2
	XM_017027201.1	4	2027	XP_016882690.1
	XM_017027202.1	4	2150	XP_016882691.1
	XM_017027203.1	2	1930	XP_016882692.1
	XM_017027204.1			XP_016882693.1
	AK128184.1	4	2084
	AK131527.1	4	2125	BAD18665.1
	AK311130.1	1	852
	BX647526.1	4	2195

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv578950	Chr.19:21206193 - 21294629 on Build GRCh38	Loss	ZNF708
esv2718325	Chr.19:21119097 - 21656664 on Build GRCh38	Deletion	ZNF429 LOC105372321 ZNF493 ZNF431 ZNF708 LINC00664 ZNF714 LOC400682 ZNF738 LOC101929007
esv2751783	Chr.19:21283020 - 21543535 on Build GRCh38	Loss	ZNF429 LOC105372321 ZNF493 ZNF708 LINC00664 ZNF738
esv2665276	Chr.19:21082662 - 21397631 on Build GRCh38	Deletion	ZNF493 ZNF431 ZNF708 ZNF714 ZNF738
nsv578809	Chr.19:20352186 - 21528400 on Build GRCh38	Gain	ZNF429 ZNF430 LOC105372321 ZNF493 ZNF431 LOC105372319 ZNF714 LOC105372315 ZNF738 MIR1270 ZNF626 ZNF708 ZNF826P LINC00664 ZNF85 ZNF737
nsv1061327	Chr.19:21059770 - 22484758 on Build GRCh38	Gain	LOC105376917 ZNF429 ZNF43 LOC641367 ZNF430 LOC105372321 ZNF493 ZNF431 ZNF98 ZNF714 LOC400682 ZNF738 ZNF729 ZNF676 ZNF708 LINC00664 ZNF208 ZNF100 LOC101929007 ZNF257
esv3893179	Chr.19:21236750 - 21304570 on Build GRCh38	Loss	ZNF708

More Information

Additional Information:

For this assay, SNP(s) [rs115298258] 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

Panther Classification:

Molecular Function -

DNA-binding transcription factor, C2H2 zinc finger transcription factor

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated

Function(s)

RNA polymerase II core promoter proximal region sequence-specific DNA binding
metal ion binding