Hs03331558_cn

• Gene Symbol: GPR153
• Assay Reference Genome Location: Chr.1:6252100 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 3

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_017001250.1			XP_016856739.1
	XM_017001251.1			XP_016856740.1
	AY255529.1			AAO85041.1
	BC068275.1			AAH68275.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv8n67	Chr.1:6220621 - 6264303 on Build GRCh38	Gain	ACOT7 HES3 RNF207 GPR153 LINC00337 ICMT
nsv526371	Chr.1:6247195 - 6307159 on Build GRCh38	Loss	ACOT7 GPR153
nsv831425	Chr.1:6129291 - 6264418 on Build GRCh38	Loss	CHD5 ACOT7 HES3 LOC102724450 RNF207 GPR153 RPL22 LINC00337 ICMT
nsv545236	Chr.1:6161915 - 6262876 on Build GRCh38	Loss	CHD5 HES3 LOC102724450 RNF207 GPR153 RPL22 LINC00337 ICMT
nsv545238	Chr.1:6248510 - 6257923 on Build GRCh38	Loss	GPR153
nsv508825	Chr.1:6221275 - 6286549 on Build GRCh38	Insertion	ACOT7 HES3 RNF207 GPR153 LINC00337 ICMT

More Information

Additional Information:

For this assay, SNP(s) [rs78137903] 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