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

Chr.9:137033161 on build GRCh38
Cytoband
9q34.3
Assay ID Hs00528576_cn
Size
Availability Made To Order
Catalog # 4400291
Price 457.00
Your Price
Online offer: 424.65
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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 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C9orf139 NM_207511.2 2 1612 NP_997394.1
XM_017014717.1 2 577 XP_016870206.1
AK093587.1 BAC04202.1
AK124899.1 2 1612 BAC85986.1
BC132809.1 1 386
BC136839.1 1 386

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

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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