Hs01614255_cn

• Gene Symbol: ASB8
• Assay Reference Genome Location: Chr.12:48148236 on build GRCh38
• Cytoband: 12q13.11

Target Gene Details

• Entrez Gene ID: 140461
• Gene Name: ankyrin repeat and SOCS box containing 8
• Gene Aliases: PP14212
• Location: Chr.12:48147788-48157595 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ASB8	NM_001319296.1	5	2303	NP_001306225.1
	NM_001319297.1	4	2163	NP_001306226.1
	NM_001319298.1	5	2268	NP_001306227.1
	NM_001319299.1	5	2264	NP_001306228.1
	NM_001319300.1	5	2221	NP_001306229.1
	NM_001319301.1	5	2217	NP_001306230.1
	NM_024095.4	4	2167	NP_077000.1
	AF464877.1	4	2059	AAQ04830.1
	AW292787.1	1	463
	BQ009637.1	1	464

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2759898	Chr.12:48035919 - 48431716 on Build GRCh38	Gain+Loss	C12orf54 MIR6505 SENP1 ASB8 H1FNT CCDC184 ZNF641 OR10AD1 PFKM
esv3629429	Chr.12:48142951 - 48278499 on Build GRCh38	Gain	ASB8 CCDC184 OR10AD1 PFKM
nsv508673	Chr.12:48096003 - 48173355 on Build GRCh38	Deletion	MIR6505 SENP1 ASB8 PFKM
nsv8971	Chr.12:48142743 - 48364718 on Build GRCh38	Gain+Loss	ASB8 H1FNT CCDC184 ZNF641 OR10AD1 PFKM
esv34439	Chr.12:48147974 - 48385779 on Build GRCh38	Gain	ASB8 H1FNT CCDC184 ZNF641 OR10AD1

More Information

Additional Information:

For this assay, SNP(s) [rs74089125] 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, DGV Variation

Gene Ontology Categories:

Process(es)

protein ubiquitination
intracellular signal transduction