Hs01161449_cn

• Gene Symbol: ENO3
• Assay Reference Genome Location: Chr.17:4952838 on build GRCh38
• Cytoband: 17p13.2

Target Gene Details

• Entrez Gene ID: 2027
• Gene Name: enolase 3
• Gene Aliases: GSD13, MSE
• Location: Chr.17:4949182-4957131 on Build GRCh38
• Assay Gene Location: Overlaps Intron 4 - Exon 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ENO3	NM_001193503.1			NP_001180432.1
	NM_001976.4			NP_001967.3
	NM_053013.3			NP_443739.3
	XM_005256521.2			XP_005256578.1
	XM_011523729.1			XP_011522031.1
	XM_017024346.1			XP_016879835.1
	AK300662.1
	AK300673.1
	AK300709.1
	AK309864.1
	AU143784.1
	BC017249.2			AAH17249.1
	BJ995304.1
	DA082822.1
	DA566866.1
	X16504.1			CAA34513.1
	X51957.1			CAA36216.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv833350	Chr.17:4884713 - 5060776 on Build GRCh38	Loss	LOC101927979 INCA1 CAMTA2 PFN1 SLC52A1 LOC102724009 ENO3 KIF1C MIR6864 RNF167 MINK1 SPAG7 GP1BA CHRNE C17orf107 MIR6865 SLC25A11
nsv833349	Chr.17:4853631 - 4991300 on Build GRCh38	Loss	LOC101927979 INCA1 CAMTA2 PFN1 ENO3 MIR6864 RNF167 MINK1 SPAG7 GP1BA CHRNE C17orf107 MIR6865 SLC25A11
nsv833347	Chr.17:4785297 - 4955981 on Build GRCh38	Loss	LOC107984973 PLD2 PFN1 ENO3 GLTPD2 RNF167 VMO1 MINK1 GP1BA CHRNE C17orf107 SLC25A11 PSMB6
nsv574273	Chr.17:4585589 - 5460332 on Build GRCh38	Gain	LOC101927979 DHX33 LOC107984973 LOC101559451 C1QBP ZNF232 USP6 RPAIN ENO3 KIF1C SMTNL2 MINK1 SPAG7 CHRNE TM4SF5 SLC25A11 LOC101928000 PSMB6 ARRB2 LOC400568 INCA1 CAMTA2 ALOX15 CXCL16 PLD2 PFN1 LOC100130950 SLC52A1 LOC102724009 MED11 MIR6864 GLTPD2 RABEP1 ZMYND15 ZNF594 RNF167 VMO1 NUP88 GP1BA C17orf107 ZFP3 PELP1 SCIMP MIR6865

More Information

Additional Information:

For this assay, SNP(s) [rs151153333] 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

Panther Classification:

Molecular Function -

lyase

Gene Ontology Categories:

Process(es)

gluconeogenesis
aging
response to drug
skeletal muscle tissue regeneration
canonical glycolysis

Function(s)

magnesium ion binding
phosphopyruvate hydratase activity
protein homodimerization activity
protein heterodimerization activity