Hs03357766_cn

• Gene Symbol: GPR153
• Assay Reference Genome Location: Chr.1:6259800 on build GRCh38
• Cytoband: 1p36.31

Target Gene Details

• Entrez Gene ID: 387509
• Gene Name: G protein-coupled receptor 153
• Gene Aliases: PGR1
• Location: Chr.1:6247346-6260975 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GPR153	NM_207370.2			NP_997253.2
	XM_011541434.2			XP_011539736.1
	XM_017001251.1			XP_016856740.1
	BC068275.1			AAH68275.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv965	Chr.1:6253120 - 6297822 on Build GRCh38	Deletion	GPR153 ACOT7
dgv8n67	Chr.1:6220621 - 6264303 on Build GRCh38	Gain	GPR153 RNF207 HES3 ICMT ACOT7 LINC00337
nsv526371	Chr.1:6247195 - 6307159 on Build GRCh38	Loss	GPR153 ACOT7
nsv831425	Chr.1:6129291 - 6264418 on Build GRCh38	Loss	RPL22 GPR153 LOC102724450 RNF207 HES3 CHD5 ICMT ACOT7 LINC00337
nsv545236	Chr.1:6161915 - 6262876 on Build GRCh38	Loss	RPL22 GPR153 LOC102724450 RNF207 HES3 CHD5 ICMT LINC00337
nsv508825	Chr.1:6221275 - 6286549 on Build GRCh38	Insertion	GPR153 RNF207 HES3 ICMT ACOT7 LINC00337

More Information

Additional Information:

For this assay, SNP(s) [rs115097550] 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 -

G-protein coupled receptor

Gene Ontology Categories:

Process(es)

G-protein coupled receptor signaling pathway

Function(s)

G-protein coupled receptor activity