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Gene Symbol
ENOX1
Assay Reference Genome
Location

Chr.13:43243296 on build GRCh38
Cytoband
13q14.11
Assay ID Hs03848132_cn
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Availability Made To Order
Catalog # 4400291
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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 DNAJC15 ENOX1 LINC00400
esv3631919 Chr.13:43144920 - 43295829 on Build GRCh38 Gain ENOX1 LINC00400
dgv329e214 Chr.13:42914540 - 43294285 on Build GRCh38 Gain LOC105370178 DNAJC15 ENOX1 LINC00400 EPSTI1
dgv1637n100 Chr.13:42834264 - 43351384 on Build GRCh38 Gain LOC105370178 LINC00428 DNAJC15 ENOX1 LINC00400 EPSTI1
esv33538 Chr.13:42808106 - 43299785 on Build GRCh38 Gain LINC01050 LOC105370178 LINC00428 DNAJC15 ENOX1 LINC00400 EPSTI1
dgv1644n100 Chr.13:43202567 - 43317013 on Build GRCh38 Gain ENOX1
nsv832594 Chr.13:43135173 - 43317395 on Build GRCh38 Gain+Loss ENOX1 LINC00400
dgv3129n54 Chr.13:42767972 - 43316240 on Build GRCh38 Gain FAM216B LINC01050 LOC105370178 LINC00428 DNAJC15 ENOX1 LINC00400 EPSTI1
nsv1046164 Chr.13:43168728 - 43364405 on Build GRCh38 Gain ENOX1

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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:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

oxidoreductase

Gene Ontology Categories:

Function(s) Process(es)


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