Product Details

Assay Reference Genome
Location

Chr.2:213291507 on build GRCh38

Cytoband

2q34

Species

Homo sapiens

Variation Type

Copy Number

Additional Information

For this assay, SNP(s) [rs115093595] 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

79582

Gene Symbol

SPAG16

Gene Name

sperm associated antigen 16

Gene Aliases

PF20, WDR29

Location

Chr.2:213284369-214410501 on build GRCh38

Assay Gene Location

Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
SPAG16	NM_001025436.2			NP_001020607.1
	NM_024532.4			NP_078808.3
	NR_047659.1
	NR_047660.1
	XM_006712746.2			XP_006712809.1
	XM_011511814.1			XP_011510116.1
	XM_011511815.1			XP_011510117.1
	XM_011511816.2			XP_011510118.1
	XM_011511817.1			XP_011510119.1
	XM_011511818.1			XP_011510120.1
	XM_011511820.1			XP_011510122.1
	XM_011511821.2			XP_011510123.1
	XM_011511822.1			XP_011510124.1
	XM_011511824.1			XP_011510126.1
	XM_011511827.1			XP_011510129.1
	XM_011511828.1			XP_011510130.1
	XM_011511829.1			XP_011510131.1
	XM_011511831.1			XP_011510133.1
	XM_011511832.1			XP_011510134.1
	XM_011511835.2			XP_011510137.1
	XM_011511837.2			XP_011510139.1
	XM_017004896.1			XP_016860385.1
	XM_017004899.1			XP_016860388.1
	XM_017004900.1			XP_016860389.1
	XM_017004901.1			XP_016860390.1
	AF310672.1			AAM63956.1
	AF426740.1			AAN63530.1
	AF490390.1			AAM97147.1
	AK026377.1			BAB15466.1
	AK095036.1			BAC04481.1
	AK302351.1
	AK310883.1
	AL832962.1			CAH56274.1
	BC009614.1			AAH09614.1
	BC025379.1			AAH25379.1
	BC067756.1			AAH67756.1
	BC100282.1			AAI00283.1
	CR457359.1			CAG33640.1
	CR749477.1			CAH18307.1

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