Hs02969552_cn

• Gene Symbol: ADGRF3
• Assay Reference Genome Location: Chr.2:26316342 on build GRCh38
• Cytoband: 2p23.3

Target Gene Details

• Entrez Gene ID: 165082
• Gene Name: adhesion G protein-coupled receptor F3
• Gene Aliases: GPR113, PGR23
• Location: Chr.2:26308173-26346817 on Build GRCh38
• Assay Gene Location: Within Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ADGRF3	NM_001145168.1	5	609	NP_001138640.1
	NM_001145169.1	4	455	NP_001138641.1
	NM_001321971.1	4	1015	NP_001308900.1
	NM_001321975.1	4	450	NP_001308904.1
	NM_153835.3			NP_722577.2
	NR_135916.1
	XM_011532621.2	4	940	XP_011530923.1
	XM_011532622.2	4	892	XP_011530924.1
	XM_011532623.2	4	884	XP_011530925.1
	XM_017003505.1	4	926	XP_016858994.1
	XM_017003506.1	4	1182	XP_016858995.1
	AK122995.1
	AK293887.1	4	455
	AY140955.1	5	609	AAN46669.1
	AY358172.1			AAQ88539.1
	AY358214.1			AAQ88581.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv953758	Chr.2:26310833 - 26320232 on Build GRCh38	Deletion	ADGRF3
esv33316	Chr.2:25440017 - 26672800 on Build GRCh38	Loss	DRC1 RAB10 ADGRF3 GAREM2 CIB4 DTNB EPT1 OTOF KIF3C ASXL2 C2orf70 HADHB HADHA

More Information

Additional Information:

For this assay, SNP(s) [rs79188484] 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)

cell surface receptor signaling pathway
G-protein coupled receptor signaling pathway

Function(s)

G-protein coupled receptor activity