Hs03627475_cn

• Gene Symbol: FAM185A
• Assay Reference Genome Location: Chr.7:102812176 on build GRCh38
• Cytoband: 7q22.1

Target Gene Details

• Entrez Gene ID: 222234
• Gene Name: family with sequence similarity 185 member A
• Gene Aliases: -
• Location: Chr.7:102748944-102913394 on Build GRCh38
• Assay Gene Location: Within Intron 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM185A	XM_006715896.3			XP_006715959.1
	XM_011515922.2			XP_011514224.1
	XM_011515923.2			XP_011514225.1
	XM_011515924.2			XP_011514226.1
	XM_011515925.2			XP_011514227.1
	XM_011515926.2			XP_011514228.1
	XM_017011846.1			XP_016867335.1
	XM_017011847.1			XP_016867336.1
	XM_017011848.1			XP_016867337.1
	XM_017011849.1			XP_016867338.1
	AK297455.1

Target Gene Details

• Entrez Gene ID: 222235
• Gene Name: F-box and leucine rich repeat protein 13
• Gene Aliases: DRC6, Fbl13
• Location: Chr.7:102699226-103074841 on Build GRCh38
• Assay Gene Location: Within Exon 29

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FBXL13	XM_005250205.3	21	3707	XP_005250262.1
	XM_005250207.3	20	3608	XP_005250264.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2761100	Chr.7:102695340 - 102841531 on Build GRCh38	Gain+Loss	FBXL13 FAM185A
nsv469620	Chr.7:102655945 - 102813616 on Build GRCh38	Loss	FBXL13 FAM185A POLR2J2 SPDYE2B
nsv608057	Chr.7:102799737 - 102898068 on Build GRCh38	Loss	FBXL13 FAM185A
esv3614358	Chr.7:102794927 - 102853299 on Build GRCh38	Gain	FBXL13 FAM185A
nsv470382	Chr.7:102735216 - 102898068 on Build GRCh38	Loss	FBXL13 FAM185A
dgv6538n100	Chr.7:102171110 - 103063688 on Build GRCh38	Gain	UPK3BL NFE4 MIR5090 RASA4 MIR4467 LRWD1 ALKBH4 FBXL13 MIR4285 CUX1 FAM185A POLR2J LOC100289561 PRKRIP1 LOC107983993 SH2B2 LOC102724229 POLR2J2 ORAI2 LRRC17 LOC100630923 RASA4B POLR2J3 SPDYE2B SPDYE6 SPDYE2 MIR548O
esv2752138	Chr.7:102717873 - 103146688 on Build GRCh38	Loss	FBXL13 NFE4 FAM185A ARMC10 NAPEPLD LRRC17 RPL19P12

More Information

Additional Information:

For this assay, SNP(s) [rs115121768] 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, Intronic, Non-exonic, DGV Variation