Hs07094679_cn

• Gene Symbol: GPATCH2L
• Assay Reference Genome Location: Chr.14:76165668 on build GRCh38
• Cytoband: 14q24.3

Target Gene Details

• Entrez Gene ID: 55668
• Gene Name: G-patch domain containing 2 like
• Gene Aliases: C14orf118
• Location: Chr.14:76151885-76214473 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GPATCH2L	NM_001322026.1			NP_001308955.1
	NM_001322027.1			NP_001308956.1
	NM_001322028.1			NP_001308957.1
	NM_001322029.1			NP_001308958.1
	NM_001322030.1			NP_001308959.1
	NM_001322031.1			NP_001308960.1
	NM_001322032.1			NP_001308961.1
	NM_017926.3			NP_060396.2
	NM_017972.3			NP_060442.2
	NR_110314.1
	XM_006720191.2			XP_006720254.1
	XM_017021427.1			XP_016876916.1
	XM_017021428.1			XP_016876917.1
	XM_017021429.1			XP_016876918.1
	XM_017021430.1			XP_016876919.1
	XM_017021431.1			XP_016876920.1
	XM_017021432.1			XP_016876921.1
	XM_017021433.1			XP_016876922.1
	AB032978.1			BAA86466.1
	AK000696.1			BAA91325.1
	AK000895.1			BAA91411.1
	AK023523.1
	BC058032.1			AAH58032.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3581315	Chr.14:76155402 - 76173245 on Build GRCh38	Loss	GPATCH2L

More Information

Additional Information:

For this assay, SNP(s) [rs79557908] 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 -

RNA metabolism protein

Gene Ontology Categories:

Function(s)

protein binding