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See other NOXA1 CNV Assays ›
Gene Symbol
NOXA1
Assay Reference Genome
Location

Chr.9:137424035 on build GRCh38
Cytoband
9q34.3
Assay ID Hs03722622_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 10811

Gene Name:

 NADPH oxidase activator 1

Gene Aliases:

 NY-CO-31, SDCCAG31, p51NOX

Location:

 Chr.9:137423372-137434406 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NOXA1 NM_001256067.1 NP_001242996.1
NM_001256068.1 NP_001242997.1
NM_006647.1 NP_006638.1
XM_011518158.2 XP_011516460.1
XM_011518159.1 XP_011516461.1
XM_011518160.1 XP_011516462.1
AB095031.1 BAC76710.1
AK098341.1
AY255769.1 AAP13480.1
AY927790.1 AAY16126.1
AY927791.1 AAY16127.1
BC041594.1 AAH41594.1
BC110840.1 AAI10841.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1049808 Chr.9:137356366 - 137438026 on Build GRCh38 Gain EXD3 ENTPD8 NOXA1
nsv951208 Chr.9:137379349 - 137467948 on Build GRCh38 Deletion EXD3 NSMF PNPLA7 ENTPD8 MIR7114 NOXA1
nsv524322 Chr.9:136795692 - 137482216 on Build GRCh38 Loss NPDC1 C9orf172 PRR31 FUT7 TUBB4B RABL6 TMEM203 MIR4292 TRAF2 MIR4479 GRIN1 ENTPD8 STPG3 CCDC183-AS1 NOXA1 C9orf173-AS1 MAN1B1 RNF224 CCDC183 NDOR1 TOR4A UAP1L1 SSNA1 PTGDS LRRC26 MIR3621 TMEM210 ANAPC2 MAN1B1-AS1 SAPCD2 MAMDC4 ENTPD2 EXD3 PHPT1 MIR7114 NELFB TPRN LCNL1 RNF208 C8G NSMF EDF1 PNPLA7 FBXW5 LOC101930307 CYSRT1 NRARP C9orf139 ABCA2 FAM166A DPP7 CLIC3 LCN12 C9orf142 SLC34A3
esv2759721 Chr.9:137303332 - 137447299 on Build GRCh38 Loss EXD3 ENTPD8 NOXA1
nsv6771 Chr.9:137412670 - 137444666 on Build GRCh38 Insertion EXD3 ENTPD8 NOXA1
esv3573431 Chr.9:137415581 - 137425256 on Build GRCh38 Loss EXD3 NOXA1
nsv1161918 Chr.9:137118319 - 137438026 on Build GRCh38 Duplication ANAPC2 NDOR1 TOR4A TUBB4B SSNA1 CYSRT1 NRARP TMEM203 EXD3 LRRC26 FAM166A GRIN1 ENTPD8 MIR3621 NELFB STPG3 NOXA1 SLC34A3 C9orf173-AS1 TPRN RNF208 TMEM210 RNF224

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More Information


Additional Information:

For this assay, SNP(s) [rs116280312] 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:

Function(s) Process(es)


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