Hs07179699_cn

• Gene Symbol: SLX4IP
• Assay Reference Genome Location: Chr.20:10459655 on build GRCh38
• Cytoband: 20p12.2

Target Gene Details

• Entrez Gene ID: 128710
• Gene Name: SLX4 interacting protein
• Gene Aliases: C20orf94, bA204H22.1, bA254M13.1, dJ1099D15.3
• Location: Chr.20:10434453-10628138 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLX4IP	NM_001009608.2			NP_001009608.1
	XM_017027648.1			XP_016883137.1
	XM_017027650.1			XP_016883139.1
	XM_017027652.1			XP_016883141.1
	BC020787.1
	BC026094.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv522874	Chr.20:9918791 - 10838562 on Build GRCh38	Loss	MIR6870 LOC101929395 SNAP25 LOC101929371 JAG1 LOC105372526 SNAP25-AS1 MKKS SLX4IP ANKEF1

More Information

Additional Information:

For this assay, SNP(s) [rs111791682] 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:

Function(s)

protein binding