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 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv833349 | Chr.17:4853631 - 4991300 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv833347 | Chr.17:4785297 - 4955981 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv574273 | Chr.17:4585589 - 5460332 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
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: |
![]() ![]() ![]() |
Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)