Hs02407022_cn

• Gene Symbol: ERICH3
• Assay Reference Genome Location: Chr.1:74573459 on build GRCh38
• Cytoband: 1p31.1

Target Gene Details

• Entrez Gene ID: 127254
• Gene Name: glutamate rich 3
• Gene Aliases: C1orf173
• Location: Chr.1:74568111-74674343 on Build GRCh38
• Assay Gene Location: Overlaps Intron 18 - Exon 19

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ERICH3	NM_001002912.4			NP_001002912.4
	XM_017000274.1			XP_016855763.1
	XM_017000275.1			XP_016855764.1
	XM_017000276.1			XP_016855765.1
	XM_017000277.1			XP_016855766.1
	XM_017000278.1			XP_016855767.1
	XM_017000279.1			XP_016855768.1
	XM_017000280.1			XP_016855769.1
	XM_017000281.1			XP_016855770.1
	XM_017000282.1			XP_016855771.1
	XM_017000283.1			XP_016855772.1
	XM_017000284.1			XP_016855773.1
	XM_017000285.1			XP_016855774.1
	AK127470.1			BAC86994.1
	CR749349.1			CAH18202.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv830248	Chr.1:74496707 - 74678774 on Build GRCh38	Loss	TNNI3K ERICH3-AS1 LOC105378803 FPGT-TNNI3K ERICH3
nsv1002115	Chr.1:72379872 - 74933684 on Build GRCh38	Gain	TNNI3K LINC01360 TYW3 ERICH3-AS1 CRYZ LOC105378803 LRRIQ3 FPGT FPGT-TNNI3K ERICH3 LOC339468

More Information

Additional Information:

For this assay, SNP(s) [rs77910454] 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, Non-exonic, DGV Variation