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

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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