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See other NUDT18 CNV Assays ›
Gene Symbol
NUDT18
Assay Reference Genome
Location

Chr.8:22107129 on build GRCh38
Cytoband
8p21.3
Assay ID Hs01371862_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 79873

Gene Name:

 nudix hydrolase 18

Gene Aliases:

 MTH3

Location:

 Chr.8:22106872-22110355 on Build GRCh38

Assay Gene Location:

 Within Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NUDT18 NM_024815.3 3 1262 NP_079091.3
XM_011544650.1 4 1993 XP_011542952.1
AK026147.1 2 1446 BAB15376.1
AK124446.1 4 1993 BAC85853.1
BC016902.1 3 1274 AAH16902.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv465613 Chr.8:22046701 - 22197835 on Build GRCh38 Loss FGF17 FAM160B2 BMP1 SFTPC DMTN LGI3 HR REEP4 NUDT18
nsv528590 Chr.8:22034428 - 22168131 on Build GRCh38 Loss FGF17 FAM160B2 NPM2 BMP1 SFTPC DMTN LGI3 HR REEP4 NUDT18
nsv610765 Chr.8:22043573 - 22149780 on Build GRCh38 Loss FGF17 FAM160B2 DMTN LGI3 HR REEP4 NUDT18
nsv951112 Chr.8:22023690 - 22135287 on Build GRCh38 Deletion FGF17 FAM160B2 NPM2 DMTN HR NUDT18
nsv527293 Chr.8:22106867 - 22163524 on Build GRCh38 Loss SFTPC LGI3 HR REEP4 NUDT18
nsv831263 Chr.8:22031088 - 22184413 on Build GRCh38 Loss FGF17 FAM160B2 NPM2 BMP1 SFTPC DMTN LGI3 HR REEP4 NUDT18
nsv470204 Chr.8:22094715 - 22171155 on Build GRCh38 Loss FAM160B2 BMP1 SFTPC LGI3 HR REEP4 NUDT18
dgv12054n54 Chr.8:22045805 - 22251098 on Build GRCh38 Loss FGF17 FAM160B2 MIR320A BMP1 PHYHIP SFTPC DMTN LGI3 HR POLR3D REEP4 NUDT18
nsv831264 Chr.8:22093700 - 22328040 on Build GRCh38 Gain+Loss LOC100507071 FAM160B2 MIR320A PIWIL2 BMP1 PHYHIP SFTPC LGI3 HR POLR3D REEP4 NUDT18
esv2759604 Chr.8:20675533 - 23254096 on Build GRCh38 Loss CHMP7 MIR320A LOC107986876 TNFRSF10C NPM2 BMP1 LOC101929237 LOC286059 RHOBTB2 DOK2 REEP4 EGR3 DMTN TNFRSF10B LGI3 POLR3D LOC102467222 LOC100507071 FGF17 FAM160B2 LOC107984124 PIWIL2 BIN3 SFTPC LOC389641 CCAR2 GFRA2 TNFRSF10A NUDT18 TNFRSF10D SORBS3 SLC39A14 LOC101929172 XPO7 PPP3CC BIN3-IT1 PEBP4 PHYHIP C8orf58 LOC254896 PDLIM2 LOC286114 HR

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More Information


Additional Information:

For this assay, SNP(s) [rs376806678,rs76769824] 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 Exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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