Hs02221109_cn

• Gene Symbol: DDX55
• Assay Reference Genome Location: Chr.12:123620744 on build GRCh38
• Cytoband: 12q24.31

Target Gene Details

• Entrez Gene ID: 57696
• Gene Name: DEAD-box helicase 55
• Gene Aliases: -
• Location: Chr.12:123602077-123620943 on Build GRCh38
• Assay Gene Location: Within Exon 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
DDX55	NM_020936.2	14	2479	NP_065987.1
	NR_135104.1	14	2551
	NR_135105.1	14	2463
	XM_017019710.1	14	2518	XP_016875199.1
	XM_017019711.1	13	2573	XP_016875200.1
	XM_017019712.1	14	2371	XP_016875201.1
	XM_017019713.1	14	2494	XP_016875202.1
	XM_017019714.1	15	2652	XP_016875203.1
	XM_017019715.1	12	2219	XP_016875204.1
	XM_017019716.1	12	2164	XP_016875205.1
	XM_017019717.1	14	2416	XP_016875206.1
	XM_017019718.1	12	2834	XP_016875207.1
	XM_017019719.1	14	2371	XP_016875208.1
	XM_017019720.1	12	3449	XP_016875209.1
	AA403154.1	1	204
	BU619784.1	1	208

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv1566n100	Chr.12:123610211 - 123711309 on Build GRCh38	Gain	TCTN2 GTF2H3 EIF2B1 DDX55
dgv524e212	Chr.12:123614065 - 123625575 on Build GRCh38	Loss	EIF2B1 DDX55
nsv1042181	Chr.12:123552853 - 123668403 on Build GRCh38	Gain	TMED2 LOC101927415 GTF2H3 EIF2B1 DDX55

More Information

Additional Information:

For this assay, SNP(s) [rs118095783] 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

Gene Ontology Categories:

Process(es)

RNA secondary structure unwinding

Function(s)

ATP-dependent RNA helicase activity
protein binding
ATP binding
poly(A) RNA binding