Hs06354187_cn

• Gene Symbol: WSB2
• Assay Reference Genome Location: Chr.12:118060849 on build GRCh38
• Cytoband: 12q24.23

Target Gene Details

• Entrez Gene ID: 55884
• Gene Name: WD repeat and SOCS box containing 2
• Gene Aliases: SBA2
• Location: Chr.12:118032687-118062430 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
WSB2	NM_001278557.1			NP_001265486.1
	NM_001278558.1			NP_001265487.1
	NM_018639.4			NP_061109.1
	XM_017019642.1			XP_016875131.1
	AF229181.1			AAF71302.1
	AK295555.1
	AK298513.1
	AK310892.1
	BC015887.2			AAH15887.1
	DA772463.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1126323	Chr.12:118060795 - 118061495 on Build GRCh38	Deletion	WSB2
nsv1071058	Chr.12:118060694 - 118061395 on Build GRCh38	Deletion	WSB2
esv3581916	Chr.12:117356518 - 118228514 on Build GRCh38	Gain	WSB2 KSR2 NOS1 VSIG10 TAOK3 RFC5 PEBP1

More Information

Additional Information:

For this assay, SNP(s) [rs371352502] 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)

protein ubiquitination
intracellular signal transduction