Hs04366257_cn

• Gene Symbol: AKNA
• Assay Reference Genome Location: Chr.9:114334782 on build GRCh38
• Cytoband: 9q32

Target Gene Details

• Entrez Gene ID: 80709
• Gene Name: AT-hook transcription factor
• Gene Aliases: -
• Location: Chr.9:114334149-114398498 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
AKNA	AK055563.1	1	93
	AK098036.1	1	1418

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv2181e212	Chr.9:114317539 - 114335437 on Build GRCh38	Gain	ORM1 AKNA ORM2
nsv968749	Chr.9:114324831 - 114335180 on Build GRCh38	Duplication	ORM1 AKNA ORM2
esv3576696	Chr.9:114324735 - 114335437 on Build GRCh38	Gain	ORM1 AKNA ORM2
dgv33e196	Chr.9:114030664 - 114604363 on Build GRCh38	Duplication	COL27A1 ORM1 KIF12 ATP6V1G1 AKNA ZNF618 WHRN ORM2 TMEM268 MIR455 AMBP
dgv949n27	Chr.9:114283521 - 114343856 on Build GRCh38	Gain	COL27A1 ORM1 AKNA ORM2
esv2462819	Chr.9:114327942 - 114335805 on Build GRCh38	Deletion	AKNA ORM2
esv22321	Chr.9:114320556 - 114336003 on Build GRCh38	Gain	ORM1 AKNA ORM2
dgv948n27	Chr.9:114193988 - 114693895 on Build GRCh38	Gain	COL27A1 ORM1 ATP6V1G1 AKNA WHRN ORM2 TMEM268 MIR455 LOC100505478
esv2752277	Chr.9:114323991 - 114338965 on Build GRCh38	Gain	ORM1 AKNA ORM2
esv2761285	Chr.9:114049617 - 114340988 on Build GRCh38	Gain	COL27A1 ORM1 KIF12 AKNA ZNF618 ORM2 MIR455 AMBP
nsv509319	Chr.9:114297186 - 114380605 on Build GRCh38	Insertion	COL27A1 ORM1 AKNA ORM2
dgv7706n100	Chr.9:114182745 - 114697870 on Build GRCh38	Gain	COL27A1 ORM1 ATP6V1G1 AKNA WHRN ORM2 TMEM268 MIR455 LOC100505478
esv3621554	Chr.9:114316410 - 114335883 on Build GRCh38	Loss	ORM1 AKNA ORM2
nsv471320	Chr.9:114284841 - 114346385 on Build GRCh38	Gain	COL27A1 ORM1 AKNA ORM2
nsv615233	Chr.9:114167820 - 114486199 on Build GRCh38	Gain	COL27A1 ORM1 AKNA WHRN ORM2 MIR455

More Information

Additional Information:

For this assay, SNP(s) [rs115361201] 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