accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other EME2 CNV Assays ›
Gene Symbol
EME2
Assay Reference Genome
Location

Chr.16:1773300 on build GRCh38
Cytoband
16p13.3
Assay ID Hs02944557_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 197342

Gene Name:

 essential meiotic structure-specific endonuclease subunit 2

Gene Aliases:

 SLX2B, gs125

Location:

 Chr.16:1773222-1776714 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
EME2 NM_001257370.1 1 73 NP_001244299.1
XM_017023025.1 1 79 XP_016878514.1
XM_017023026.1 1 79 XP_016878515.1
AK074080.2 BAB84906.2
EF452422.1 1 73

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv457335 Chr.16:1729694 - 1789022 on Build GRCh38 Loss NME3 EME2 MAPK8IP3 MRPS34 SPSB3 NUBP2 MIR3177
esv2422427 Chr.16:10001 - 2723164 on Build GRCh38 Duplication ZNF598 ABCA17P RNPS1 SNHG9 LOC106660606 CLCN7 CCDC154 DNASE1L2 NTN3 UBE2I MIR4717 C1QTNF8 CHTF18 HBA1 RNF151 DDX11L10 SOX8 POLR3K LOC100134368 LOC105371049 SSTR5 MIR6511B1 SLC9A3R2 NARFL MAPK8IP3 GNG13 MCRIP2 IFT140 MIR3180-5 NOXO1 WDR24 TBL3 RAB11FIP3 HBZ PTX4 METRN SSTR5-AS1 METTL26 AMDHD2 ARHGDIG HBM STUB1 NUBP2 MIR662 NME3 PKD1 TPSG1 FAHD1 SYNGR3 PRR35 LMF1-AS1 CCNF TSC2 NHLRC4 MIR3178 FAM234A NPW LOC105371045 HAGH MRPL28 PRSS27 DECR2 PIGQ RAB26 MSRB1 MEIOB LOC105371046 ABCA3 PDIA2 LINC00235 PRR25 TRAF7 WDR90 RPL23AP5 ATP6V0C MIR3677 LOC101929280 CCDC78 HS3ST6 NPRL3 LOC105371038 FBXL16 CASKIN1 LOC107987233 RPL3L MIR6859-4 NME4 C16orf91 LOC652276 KCTD5 SPSB3 C16orf59 MLST8 RPUSD1 NTHL1 CAPN15 MSLN SNORA64 PRSS29P MIR5587 HBA2 LOC107984876 LINC00254 RGS11 LOC729652 E4F1 PGP TPSD1 MPG MIR1225 MRPS34 MIR6767 WASIR2 FLJ42627 SNRNP25 TELO2 BAIAP3 LOC105371184 SNHG19 SNORD60 MIR3177 AXIN1 ECI1 CRAMP1 PDPK1 SNORA10 SNORA78 UNKL TBC1D24 HBQ1 RPS2 RAB40C HN1L LMF1 TPSAB1 WFIKKN1 GNPTG TMEM204 CEMP1 JMJD8 RHBDL1 MIR4516 EME2 NDUFB10 LUC7L LOC105371047 IGFALS TSR3 MIR6768 TMEM8A HAGHL LOC100287175 GFER ERVK13-1 TPSB2 RHOT2 BRICD5 CACNA1H RHBDF1 MIR3176 FAM173A MIR940
esv3892756 Chr.16:1764390 - 1780436 on Build GRCh38 Loss NME3 EME2 MAPK8IP3 MRPS34 SPSB3
nsv1160328 Chr.16:1704619 - 1797867 on Build GRCh38 Deletion NME3 EME2 IGFALS MAPK8IP3 MRPS34 SPSB3 NUBP2 MIR3177
nsv571171 Chr.16:1757779 - 1804539 on Build GRCh38 Gain+Loss NME3 EME2 IGFALS MAPK8IP3 MRPS34 SPSB3 NUBP2
dgv4856n54 Chr.16:1600945 - 1813519 on Build GRCh38 Loss NME3 CRAMP1 EME2 IFT140 IGFALS MRPS34 SPSB3 HN1L MAPK8IP3 HAGH NUBP2 MIR3177 LOC105371046
nsv471069 Chr.16:1754356 - 1791032 on Build GRCh38 Loss NME3 EME2 IGFALS MAPK8IP3 MRPS34 SPSB3 NUBP2
nsv1051692 Chr.16:1505070 - 1866102 on Build GRCh38 Loss NME3 CRAMP1 FAHD1 EME2 IFT140 LOC105371047 IGFALS MRPS34 SPSB3 TELO2 HN1L MAPK8IP3 HAGH NUBP2 MEIOB MIR3177 LOC105371046 TMEM204
nsv827500 Chr.16:1761258 - 1795126 on Build GRCh38 Gain NME3 EME2 IGFALS MAPK8IP3 MRPS34 SPSB3 NUBP2
nsv518641 Chr.16:1645775 - 1835631 on Build GRCh38 Loss NME3 CRAMP1 FAHD1 EME2 IGFALS MRPS34 SPSB3 HN1L MAPK8IP3 HAGH NUBP2 MEIOB MIR3177
nsv571173 Chr.16:1767596 - 1780436 on Build GRCh38 Loss NME3 EME2 MAPK8IP3 MRPS34 SPSB3
nsv952900 Chr.16:1724500 - 1827999 on Build GRCh38 Deletion NME3 FAHD1 EME2 IGFALS MAPK8IP3 HAGH MRPS34 SPSB3 NUBP2 MIR3177
nsv571170 Chr.16:1752231 - 1791032 on Build GRCh38 Loss NME3 EME2 IGFALS MAPK8IP3 MRPS34 SPSB3 NUBP2

Back To Top

More Information


Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products