Hs05444389_cn

• Gene Symbol: ATF7IP2
• Assay Reference Genome Location: Chr.16:10389117 on build GRCh38
• Cytoband: 16p13.2

Target Gene Details

• Entrez Gene ID: 80063
• Gene Name: activating transcription factor 7 interacting protein 2
• Gene Aliases: MCAF2
• Location: Chr.16:10386055-10483640 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ATF7IP2	NM_001256160.1			NP_001243089.1
	NM_024997.3			NP_079273.2
	NR_045816.1
	AK093414.1			BAC04157.1
	AK296565.1
	AK299040.1
	BC033891.1			AAH33891.1
	BI459223.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1051406	Chr.16:10365859 - 10570475 on Build GRCh38	Loss	EMP2 ATF7IP2
nsv519263	Chr.16:10386989 - 10466528 on Build GRCh38	Gain+Loss	ATF7IP2
dgv4907n54	Chr.16:10388455 - 10504610 on Build GRCh38	Loss	ATF7IP2
nsv1040428	Chr.16:10145408 - 11362136 on Build GRCh38	Gain	CLEC16A CIITA LOC107984859 TVP23A EMP2 DEXI PRM1 ATF7IP2 NUBP1 TEKT5 RMI2 TNP2 PRM3 SOCS1 MIR548H2 GRIN2A LOC105371083 PRM2
dgv2727n100	Chr.16:9914166 - 10436036 on Build GRCh38	Gain	GRIN2A ATF7IP2 IMPDH1P11

More Information

Additional Information:

For this assay, SNP(s) [rs76640481] 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

Panther Classification:

Molecular Function -

transcription cofactor

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated