Assay Details
Target Gene Details
Entrez Gene ID: | 55068 |
Gene Name: | ecto-NOX disulfide-thiol exchanger 1 |
Gene Aliases: |
CNOX, PIG38, bA64J21.1, cCNOX |
Location: |
Chr.13:43213525-43786980 on Build GRCh38 |
Assay Gene Location: | Within Intron 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ENOX1 | NM_001127615.1 | NP_001121087.1 | ||
NM_001242863.1 | NP_001229792.1 | |||
NM_017993.3 | NP_060463.2 | |||
XM_005266439.3 | XP_005266496.1 | |||
XM_011535126.2 | XP_011533428.1 | |||
XM_011535127.2 | XP_011533429.1 | |||
XM_011535128.2 | XP_011533430.1 | |||
XM_011535132.2 | XP_011533434.1 | |||
XM_017020637.1 | XP_016876126.1 | |||
XM_017020638.1 | XP_016876127.1 | |||
XM_017020639.1 | XP_016876128.1 | |||
XM_017020640.1 | XP_016876129.1 | |||
AK000956.1 | BAA91442.1 | |||
AY513282.1 | AAT08035.1 | |||
BC024178.1 | AAH24178.1 | |||
EF432052.1 | ||||
KU178683.1 | ||||
KU178684.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2751145 | Chr.13:43080522 - 43250305 on Build GRCh38 | Gain |
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esv3631919 | Chr.13:43144920 - 43295829 on Build GRCh38 | Gain |
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dgv329e214 | Chr.13:42914540 - 43294285 on Build GRCh38 | Gain |
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dgv1637n100 | Chr.13:42834264 - 43351384 on Build GRCh38 | Gain |
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esv33538 | Chr.13:42808106 - 43299785 on Build GRCh38 | Gain |
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dgv1644n100 | Chr.13:43202567 - 43317013 on Build GRCh38 | Gain |
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nsv832594 | Chr.13:43135173 - 43317395 on Build GRCh38 | Gain+Loss |
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dgv3129n54 | Chr.13:42767972 - 43316240 on Build GRCh38 | Gain |
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nsv1046164 | Chr.13:43168728 - 43364405 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs73173901] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)