Hs05345842_cn

• Gene Symbol: AVEN
• Assay Reference Genome Location: Chr.15:33885249 on build GRCh38
• Cytoband: 15q14

Target Gene Details

• Entrez Gene ID: 57099
• Gene Name: apoptosis and caspase activation inhibitor
• Gene Aliases: PDCD12
• Location: Chr.15:33858602-34074877 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
AVEN	NM_020371.2			NP_065104.1
	XM_011521818.2			XP_011520120.1
	XM_011521819.2			XP_011520121.1
	XM_011521820.1			XP_011520122.1
	AF283508.1			AAF91470.1
	BC010488.1			AAH10488.1
	BC063533.1			AAH63533.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv437798	Chr.15:33883135 - 33885515 on Build GRCh38	Loss	AVEN
nsv471235	Chr.15:33743328 - 34129750 on Build GRCh38	Gain	AVEN RYR3 CHRM5 EMC7 PGBD4
esv3636092	Chr.15:33878005 - 33890938 on Build GRCh38	Gain	AVEN
nsv1052620	Chr.15:32612402 - 34538731 on Build GRCh38	Gain	AVEN GREM1 CHRM5 ARHGAP11A MIR1233-1 FMN1 LOC101928134 SLC12A6 NOP10 SCG5 LPCAT4 LOC105370757 GOLGA8A EMC7 PGBD4 NUTM1 RYR3 KATNBL1 GOLGA8B EMC4 LOC101928042 TMCO5B LOC100131315 MIR1233-2
nsv568922	Chr.15:33883771 - 33902385 on Build GRCh38	Loss	AVEN
esv33337	Chr.15:31689863 - 34575097 on Build GRCh38	Gain+Loss	AVEN GOLGA8O ARHGAP11A FMN1 SLC12A6 NOP10 LPCAT4 LOC105370757 GOLGA8A GOLGA8K KATNBL1 LOC101060588 GOLGA8B TMCO5B LOC100131315 LOC100996255 GREM1 CHRNA7 LOC100653133 CHRM5 ULK4P1 MIR1233-1 LOC101928134 WHAMMP1 SCG5 LOC105370940 EMC7 PGBD4 NUTM1 RYR3 GOLGA8N EMC4 LOC101928042 MIR1233-2
nsv568921	Chr.15:33754434 - 33955421 on Build GRCh38	Gain	AVEN RYR3
esv3569431	Chr.15:33564570 - 35080307 on Build GRCh38	Gain	AVEN CHRM5 MIR1233-1 GJD2 SLC12A6 NOP10 LPCAT4 GOLGA8A EMC7 PGBD4 NUTM1 LOC101928174 ACTC1 RYR3 KATNBL1 GOLGA8B ZNF770 EMC4 AQR MIR1233-2
nsv1044844	Chr.15:33773323 - 34004628 on Build GRCh38	Loss	AVEN RYR3 CHRM5
nsv568920	Chr.15:33742220 - 34134417 on Build GRCh38	Gain	AVEN RYR3 CHRM5 EMC7 PGBD4
dgv4456n54	Chr.15:32604149 - 34557061 on Build GRCh38	Gain	AVEN ARHGAP11A FMN1 SLC12A6 NOP10 LPCAT4 LOC105370757 GOLGA8A KATNBL1 GOLGA8B TMCO5B LOC100131315 GREM1 CHRM5 MIR1233-1 LOC101928134 SCG5 EMC7 PGBD4 NUTM1 RYR3 GOLGA8N EMC4 LOC101928042 MIR1233-2

More Information

Additional Information:

For this assay, SNP(s) [rs75665860] 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:

Process(es)

apoptotic process
negative regulation of apoptotic process

Function(s)

protein binding