Genomic Map
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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 7 |
| 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 | |||
| XM_017020641.1 | XP_016876130.1 | |||
| XM_017020642.1 | XP_016876131.1 | |||
| AK000956.1 | BAA91442.1 | |||
| BC024178.1 | AAH24178.1 | |||
| BM834061.1 | ||||
| DA512678.1 | ||||
| DA779748.1 | ||||
| DB058776.1 |
Target Gene Details
Entrez Gene ID: | 100874130 |
Gene Name: | ENOX1 antisense RNA 2 |
Gene Aliases: |
- |
Location: |
Chr.13:43448852-43459488 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ENOX1-AS2 | NR_120399.1 | |||
| CR739820.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3892336 | Chr.13:43420155 - 43603319 on Build GRCh38 | Loss |
 ENOX1-AS2
ENOX1
|
| nsv516714 | Chr.13:43450021 - 43454653 on Build GRCh38 | Loss |
ENOX1-AS2
ENOX1
|
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Additional Information:
For this assay, SNP(s) [rs78374108,rs78516042] 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
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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