Hs03932643_cn

• Gene Symbol: DDX19B
• Assay Reference Genome Location: Chr.16:70296651 on build GRCh38
• Cytoband: 16q22.1

Target Gene Details

• Entrez Gene ID: 11269
• Gene Name: DEAD-box helicase 19B
• Gene Aliases: DBP5, DDX19, RNAh
• Location: Chr.16:70289767-70335213 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
DDX19B	NM_001257172.1			NP_001244101.1
	NM_001257173.1			NP_001244102.1
	NM_001257174.1			NP_001244103.1
	XM_011522832.2			XP_011521134.1
	XM_011522833.2			XP_011521135.1
	XM_011522834.2			XP_011521136.1
	XM_017022890.1			XP_016878379.1
	AF353720.1			AAK40102.1
	AK301938.1
	AK302107.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1061286	Chr.16:70219906 - 70297504 on Build GRCh38	Gain	SMG1P7 DDX19B LOC107984138 EXOSC6 AARS
nsv833271	Chr.16:70151791 - 70319431 on Build GRCh38	Gain+Loss	LOC100506083 CLEC18C SMG1P7 DDX19B LOC107984138 EXOSC6 LOC400541 PDPR AARS LOC105371328

More Information

Additional Information:

For this assay, SNP(s) [rs77186135] 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)

mRNA export from nucleus
RNA secondary structure unwinding
protein transport

Function(s)

RNA binding
ATP-dependent RNA helicase activity
helicase activity
protein binding
ATP binding