Hs01692266_cn

• Gene Symbol: KIAA0895L
• Assay Reference Genome Location: Chr.16:67178091 on build GRCh38
• Cytoband: 16q22.1

Target Gene Details

• Entrez Gene ID: 653319
• Gene Name: KIAA0895 like
• Gene Aliases: -
• Location: Chr.16:67175602-67183980 on Build GRCh38
• Assay Gene Location: Overlaps Intron 5 - Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
KIAA0895L	NM_001040715.1			NP_001035805.1
	AK092303.1			BAC03856.1
	AK094787.1
	AK096855.1
	AL834156.1			CAD38862.1
	BC007594.1			AAH07594.1
	BC080183.1			AAH80183.1
	BC128539.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv522852	Chr.16:67153308 - 68071571 on Build GRCh38	Gain	TRADD SLC12A4 LOC105369155 LCAT CTRL LRRC29 KCTD19 PSMB10 HSD11B2 LOC100131303 EDC4 ATP6V0D1 SLC9A5 FAM65A LOC100505942 AGRP CTCF TMEM208 LOC107984813 FBXL8 CARMIL2 GFOD2 KIAA0895L EXOC3L1 ACD ZDHHC1 C16orf86 NOL3 NRN1L CENPT FHOD1 ENKD1 THAP11 ELMO3 MIR328 NUTF2 PLEKHG4 PARD6A E2F4 TSNAXIP1 TPPP3 DUS2 PSKH1 DPEP3 DPEP2 RANBP10 HSF4 LRRC36 DDX28
nsv952044	Chr.16:67141198 - 67244397 on Build GRCh38	Deletion	MIR328 KIAA0895L TRADD EXOC3L1 E2F4 LOC105369155 NOL3 C16orf70 FHOD1 B3GNT9 LRRC29 HSF4 TMEM208 ELMO3 FBXL8
nsv827707	Chr.16:67148355 - 67289296 on Build GRCh38	Loss	MIR328 KIAA0895L TRADD PLEKHG4 EXOC3L1 E2F4 LOC105369155 SLC9A5 NOL3 C16orf70 FHOD1 B3GNT9 LRRC29 HSF4 TMEM208 ELMO3 FBXL8
nsv1160429	Chr.16:67161549 - 67220197 on Build GRCh38	Deletion	MIR328 KIAA0895L LRRC29 EXOC3L1 E2F4 LOC105369155 HSF4 ELMO3 NOL3 FBXL8
nsv524363	Chr.16:67136529 - 68071571 on Build GRCh38	Loss	TRADD SLC12A4 LOC105369155 LCAT CTRL LRRC29 KCTD19 PSMB10 HSD11B2 LOC100131303 EDC4 ATP6V0D1 SLC9A5 FAM65A LOC100505942 AGRP CTCF TMEM208 LOC107984813 FBXL8 CARMIL2 GFOD2 KIAA0895L EXOC3L1 ACD ZDHHC1 C16orf86 NOL3 C16orf70 NRN1L CENPT FHOD1 ENKD1 THAP11 ELMO3 MIR328 NUTF2 PLEKHG4 PARD6A E2F4 TSNAXIP1 TPPP3 B3GNT9 DUS2 PSKH1 DPEP3 DPEP2 RANBP10 HSF4 LRRC36 DDX28
nsv471092	Chr.16:67174030 - 67518392 on Build GRCh38	Gain	MIR328 KIAA0895L PLEKHG4 EXOC3L1 ZDHHC1 E2F4 ATP6V0D1 LOC105369155 SLC9A5 NOL3 TPPP3 FHOD1 LRRC29 LOC100505942 KCTD19 AGRP TMEM208 LRRC36 ELMO3 HSD11B2

More Information

Additional Information:

For this assay, SNP(s) [rs143977756] 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, Non-exonic, DGV Variation