Hs06670387_cn

• Gene Symbol: TATDN2
• Assay Reference Genome Location: Chr.3:10254109 on build GRCh38
• Cytoband: 3p25.3

Target Gene Details

• Entrez Gene ID: 9797
• Gene Name: TatD DNase domain containing 2
• Gene Aliases: -
• Location: Chr.3:10248493-10281222 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TATDN2	NM_014760.3			NP_055575.3
	AK289794.1
	BC090935.1			AAH90935.1
	BC101770.1			AAI01771.1
	BC101776.1			AAI01777.1
	D86972.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv436362	Chr.3:10048344 - 11860564 on Build GRCh38	Deletion	SEC13 IRAK2 FANCD2 SLC6A11 FANCD2OS HRH1 LINC00852 GHRLOS LOC101927467 MIR885 TATDN2 SLC6A1-AS1 BRK1 LINC00606 MIR378B GHRL ATG7 VHL TAMM41 ATP2B2 ATP2B2-IT2 VGLL4 SLC6A1
dgv762e201	Chr.3:10008967 - 11913136 on Build GRCh38	Deletion	SEC13 IRAK2 FANCD2 SLC6A11 FANCD2OS LINC00852 FANCD2P2 GHRLOS LOC101927467 MIR885 CIDECP LOC401052 EMC3 BRK1 MIR378B GHRL VHL VGLL4 HRH1 TATDN2 SLC6A1-AS1 LINC00606 ATG7 TAMM41 ATP2B2 ATP2B2-IT2 SLC6A1
nsv1121603	Chr.3:10071433 - 11889279 on Build GRCh38	Deletion	SEC13 IRAK2 FANCD2 SLC6A11 FANCD2OS HRH1 LINC00852 FANCD2P2 GHRLOS LOC101927467 MIR885 TATDN2 SLC6A1-AS1 BRK1 LINC00606 MIR378B GHRL ATG7 VHL TAMM41 ATP2B2 ATP2B2-IT2 VGLL4 SLC6A1
nsv436869	Chr.3:10064456 - 11877985 on Build GRCh38	Insertion	SEC13 IRAK2 FANCD2 SLC6A11 FANCD2OS HRH1 LINC00852 FANCD2P2 GHRLOS LOC101927467 MIR885 TATDN2 SLC6A1-AS1 BRK1 LINC00606 MIR378B GHRL ATG7 VHL TAMM41 ATP2B2 ATP2B2-IT2 VGLL4 SLC6A1
nsv1073204	Chr.3:9996548 - 11875005 on Build GRCh38	Deletion	SEC13 IRAK2 FANCD2 SLC6A11 FANCD2OS LINC00852 FANCD2P2 GHRLOS LOC101927467 MIR885 CIDECP LOC401052 EMC3 BRK1 MIR378B GHRL VHL VGLL4 EMC3-AS1 HRH1 TATDN2 SLC6A1-AS1 LINC00606 ATG7 TAMM41 ATP2B2 ATP2B2-IT2 SLC6A1

More Information

Additional Information:

For this assay, SNP(s) [rs113207620] 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

Gene Ontology Categories:

Process(es)

DNA catabolic process
IRE1-mediated unfolded protein response
nucleic acid phosphodiester bond hydrolysis

Function(s)

deoxyribonuclease activity
endodeoxyribonuclease activity, producing 5'-phosphomonoesters
metal ion binding