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See other C9ORF139 CNV Assays ›
Gene Symbol
C9orf139
Assay Reference Genome
Location

Chr.9:137037078 on build GRCh38
Cytoband
9q34.3
Assay ID Hs03711746_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 401563

Gene Name:

 chromosome 9 open reading frame 139

Gene Aliases:

 -

Location:

 Chr.9:137027464-137037770 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C9orf139 XM_017014717.1 3 3076 XP_016870206.1

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

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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