Hs05348650_cn

• Gene Symbol: LYSMD4
• Assay Reference Genome Location: Chr.15:99726711 on build GRCh38
• Cytoband: 15q26.3

Target Gene Details

• Entrez Gene ID: 145748
• Gene Name: LysM domain containing 4
• Gene Aliases: -
• Location: Chr.15:99715033-99733561 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LYSMD4	XM_006720397.3			XP_006720460.2
	XM_011521242.2			XP_011519544.1
	XM_011521243.2			XP_011519545.1
	XM_011521245.2			XP_011519547.1
	AK056718.1
	BX640928.1			CAE45966.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv4769n54	Chr.15:99700705 - 100224933 on Build GRCh38	Gain	LOC105371022 ADAMTS17 LYSMD4 LOC400464 MEF2A DNM1P46
esv3637430	Chr.15:99708759 - 100311912 on Build GRCh38	Gain	LOC105371022 ADAMTS17 LYSMD4 LOC400464 MEF2A DNM1P46
nsv428313	Chr.15:99695998 - 100216834 on Build GRCh38	Gain	LOC105371022 ADAMTS17 LYSMD4 LOC400464 MEF2A DNM1P46
nsv1045838	Chr.15:99702862 - 100492013 on Build GRCh38	Gain	CERS3 SPATA41 LOC105371022 ADAMTS17 CERS3-AS1 LYSMD4 LOC400464 MEF2A DNM1P46

More Information

Additional Information:

For this assay, SNP(s) [rs72760585] 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