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See other ENTPD2 CNV Assays ›
Gene Symbol
ENTPD2
Assay Reference Genome
Location

Chr.9:137049412 on build GRCh38
Cytoband
9q34.3
Assay ID Hs03704770_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 954

Gene Name:

 ectonucleoside triphosphate diphosphohydrolase 2

Gene Aliases:

 CD39L1, NTPDase-2

Location:

 Chr.9:137048098-137054051 on Build GRCh38

Assay Gene Location:

 Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ENTPD2 NM_001246.3 NP_001237.1
NM_203468.2 NP_982293.1
XM_011519212.2 XP_011517514.1
AF144748.1 AAD40239.1
BC035738.1 AAH35738.1
EF495152.1
U91510.1 AAB81013.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv13007n54 Chr.9:136966179 - 137173890 on Build GRCh38 Loss CLIC3 DPP7 GRIN1 TMEM210 PRR31 LOC101930307 NPDC1 ENTPD2 PTGDS C9orf139 MIR3621 MAN1B1-AS1 FUT7 SAPCD2 UAP1L1 LRRC26 C9orf142 MAN1B1 ABCA2 LCNL1
nsv524322 Chr.9:136795692 - 137482216 on Build GRCh38 Loss RNF224 PNPLA7 PHPT1 STPG3 MIR4479 NSMF ANAPC2 MAN1B1-AS1 FUT7 EDF1 CLIC3 CYSRT1 MIR4292 C9orf172 TMEM203 EXD3 LOC101930307 NPDC1 NDOR1 TRAF2 CCDC183-AS1 C9orf142 RNF208 TOR4A LCNL1 DPP7 MAMDC4 TMEM210 ENTPD8 MIR7114 CCDC183 LCN12 ENTPD2 RABL6 PTGDS C9orf139 MIR3621 SLC34A3 TPRN C9orf173-AS1 UAP1L1 TUBB4B LRRC26 MAN1B1 NRARP FBXW5 GRIN1 PRR31 FAM166A C8G SSNA1 NOXA1 SAPCD2 NELFB ABCA2
nsv951206 Chr.9:136944849 - 137114548 on Build GRCh38 Deletion CLIC3 DPP7 PRR31 C8G LOC101930307 NPDC1 LCN12 ENTPD2 PTGDS C9orf139 MAN1B1-AS1 FUT7 SAPCD2 UAP1L1 C9orf142 MAN1B1 ABCA2 LCNL1
nsv469918 Chr.9:136359865 - 137173890 on Build GRCh38 Loss TMEM141 INPP5E FAM69B PHPT1 MIR4674 SNORA17A HSPC324 LCN8 MIR4479 DNLZ MAN1B1-AS1 FUT7 NOTCH1 LOC100128593 SNAPC4 EDF1 CLIC3 MIR4292 C9orf172 MIR126 LOC101930307 NPDC1 SDCCAG3 TRAF2 CCDC183-AS1 C9orf142 LCNL1 SEC16A SNORA17B EGFL7 DPP7 MAMDC4 TMEM210 NALT1 LCN10 LINC01451 CCDC183 LCN12 CARD9 ENTPD2 RABL6 LCN15 PTGDS C9orf139 MIR3621 UAP1L1 LRRC26 MAN1B1 MIR6722 FBXW5 GRIN1 AGPAT2 LCN6 PRR31 C8G PMPCA C9orf163 SNHG7 SAPCD2 ABCA2 MIR4673
nsv616005 Chr.9:137036493 - 137173890 on Build GRCh38 Loss DPP7 GRIN1 TMEM210 LOC101930307 NPDC1 ENTPD2 C9orf139 MIR3621 MAN1B1-AS1 SAPCD2 UAP1L1 LRRC26 MAN1B1
esv2761561 Chr.9:137030185 - 137191593 on Build GRCh38 Gain DPP7 GRIN1 TMEM210 LOC101930307 NPDC1 ENTPD2 SSNA1 C9orf139 MIR3621 ANAPC2 MAN1B1-AS1 FUT7 SAPCD2 UAP1L1 LRRC26 MAN1B1
nsv616004 Chr.9:137014976 - 137053021 on Build GRCh38 Loss C9orf139 FUT7 NPDC1 ABCA2 ENTPD2
esv2422220 Chr.9:136584135 - 137350098 on Build GRCh38 Deletion RNF224 TMEM141 FAM69B PHPT1 SNORA17A HSPC324 LCN8 STPG3 MIR4479 ANAPC2 MAN1B1-AS1 FUT7 LOC100128593 EDF1 CLIC3 CYSRT1 MIR4292 C9orf172 MIR126 TMEM203 EXD3 LOC101930307 NPDC1 NDOR1 TRAF2 CCDC183-AS1 C9orf142 RNF208 TOR4A LCNL1 SNORA17B EGFL7 DPP7 MAMDC4 TMEM210 LCN10 LINC01451 CCDC183 LCN12 ENTPD2 RABL6 LCN15 PTGDS C9orf139 MIR3621 SLC34A3 TPRN C9orf173-AS1 UAP1L1 TUBB4B LRRC26 MAN1B1 NRARP MIR6722 FBXW5 GRIN1 AGPAT2 LCN6 PRR31 FAM166A C8G SSNA1 SNHG7 SAPCD2 NELFB ABCA2

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More Information


Additional Information:

For this assay, SNP(s) [rs117662508] 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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