Hs03734496_cn

• Gene Symbol: LRRC18
• Assay Reference Genome Location: Chr.10:48906207 on build GRCh38
• Cytoband: 10q11.23

Target Gene Details

• Entrez Gene ID: 474354
• Gene Name: leucine rich repeat containing 18
• Gene Aliases: UNQ933, UNQ9338, VKGE9338
• Location: Chr.10:48881011-48940126 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LRRC18

Target Gene Details

• Entrez Gene ID: 57705
• Gene Name: WDFY family member 4
• Gene Aliases: C10orf64
• Location: Chr.10:48684815-48982956 on Build GRCh38
• Assay Gene Location: Within Intron 53

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
WDFY4	NM_020945.1			NP_065996.1
	XM_005270004.3			XP_005270061.1
	XM_011539986.2			XP_011538288.2
	XM_011539987.2			XP_011538289.2
	XM_011539988.2			XP_011538290.1
	XM_017016463.1			XP_016871952.1
	XM_017016464.1			XP_016871953.1
	AB046827.1			BAB13433.1
	AK074085.1			BAB84911.1
	AK074443.1
	AL833669.1
	BC047574.1			AAH47574.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv831865	Chr.10:48786209 - 48956194 on Build GRCh38	Gain	WDFY4 LRRC18
nsv1042677	Chr.10:47993784 - 49928329 on Build GRCh38	Loss	VSTM4 FRMPD2 ARHGAP22 C10orf128 FAM170B FAM25C LRRC18 OGDHL C10orf53 FAM170B-AS1 PGBD3 C10orf71-AS1 WDFY4 PARG SLC18A3 DRGX MIR4294 C10orf71 MAPK8 ERCC6 AGAP12P CHAT

More Information

Additional Information:

For this assay, SNP(s) [rs144532012] 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)

phospholipid binding