Hs01213562_cn

• Gene Symbol: GPRIN3
• Assay Reference Genome Location: Chr.4:89249596 on build GRCh38
• Cytoband: 4q22.1

Target Gene Details

• Entrez Gene ID: 285513
• Gene Name: GPRIN family member 3
• Gene Aliases: GRIN3
• Location: Chr.4:89237666-89308010 on Build GRCh38
• Assay Gene Location: Within Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GPRIN3	NM_198281.2	2	1034	NP_938022.2
	XM_005262936.3	2	1274	XP_005262993.1
	XM_005262937.4	2	1328	XP_005262994.1
	XM_017008043.1	2	3111	XP_016863532.1
	XM_017008044.1	2	832	XP_016863533.1
	AB095947.2	1	1599
	AK124616.1	2	817	BAC85902.1
	BC126371.1	1	648

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3569577	Chr.4:89026064 - 89372742 on Build GRCh38	Loss	GPRIN3 TIGD2 FAM13A
nsv1012406	Chr.4:89246630 - 90245636 on Build GRCh38	Loss	GPRIN3 CCSER1 SNCA-AS1 MMRN1 SNCA
nsv470051	Chr.4:88723780 - 89721993 on Build GRCh38	Gain	GPRIN3 FAM13A-AS1 TIGD2 FAM13A
nsv830002	Chr.4:89135081 - 89337714 on Build GRCh38	Gain	GPRIN3
nsv594806	Chr.4:88621130 - 90539537 on Build GRCh38	Gain	GPRIN3 FAM13A-AS1 CCSER1 TIGD2 FAM13A SNCA-AS1 MMRN1 HERC3 NAP1L5 SNCA

More Information

Additional Information:

For this assay, SNP(s) [rs72869899] 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