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