Product Details

Assay Reference Genome Location: Chr.19:46744857 on build GRCh38
Cytoband: 19q13.32
Species: Homo sapiens
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs111476621] 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.

Target Gene Details

Entrez Gene ID: 29888
Gene Symbol: STRN4
Gene Name: striatin 4
Gene Aliases: PPP2R6C, ZIN, zinedin
Location: Chr.19:46719509-46746475 on build GRCh38
Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Protein ID
STRN4	NM_001039877.1	NP_001034966.1
	NM_013403.2	NP_037535.2
	XM_006723171.2	XP_006723234.1
	XM_006723172.2	XP_006723235.1
	XM_011526878.1	XP_011525180.1
	XM_017026719.1	XP_016882208.1
	AB209003.1	BAD92240.1
	AF212940.1	AAF29527.1
	AK297637.1
	AK298804.1
	BC034604.1	AAH34604.1
	DA510367.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833850	Chr19:46703285 - 46867053 on Build GRCh38	Loss	FKRP MIR320E AP2S1 ARHGAP35 LOC107987269 SNAR-E SLC1A5 STRN4 PRKD2

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