Hs02540948_cn

• Gene Symbol: ARMCX5-GPRASP2
• Assay Reference Genome Location: Chr.X:102717633 on build GRCh38
• Cytoband: Xq22.1

Target Gene Details

• Entrez Gene ID: 100528062
• Gene Name: ARMCX5-GPRASP2 readthrough
• Gene Aliases: -
• Location: Chr.X:102599348-102717733 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ARMCX5-GPRASP2	NM_001199818.1	7	3840	NP_001186747.1

Target Gene Details

• Entrez Gene ID: 114928
• Gene Name: G protein-coupled receptor associated sorting protein 2
• Gene Aliases: GASP2
• Location: Chr.X:102712176-102717733 on Build GRCh38
• Assay Gene Location: Within Exon 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GPRASP2	NM_001004051.3	5	3708	NP_001004051.1
	NM_001184874.2	5	3836	NP_001171803.1
	NM_001184875.2	4	3748	NP_001171804.1
	NM_001184876.2	5	3747	NP_001171805.1
	NM_138437.5	4	3620	NP_612446.1
	AA906216.1	1	111
	AK092981.1	1	796
	AK094646.1	2	2006
	AK096067.1	1	2958
	AK123832.1	4	3620
	BC013576.1	1	2952	AAH13576.1
	BC036772.1	4	3384	AAH36772.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv526716	Chr.X:102582805 - 102934382 on Build GRCh38	Gain	GPRASP1 GPRASP2 ARMCX5-GPRASP2 LINC00630 BHLHB9 ARMCX5

More Information

Additional Information:

For this assay, SNP(s) [rs113047800] 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

Panther Classification:

Molecular Function -

basic helix-loop-helix transcription factor

Gene Ontology Categories:

Function(s)

beta-amyloid binding
protein binding