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Gene Symbol
GNG13
Assay Reference Genome
Location

Chr.16:800684 on build GRCh38
Cytoband
16p13.3
Assay ID Hs01758980_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 51764

Gene Name:

 G protein subunit gamma 13

Gene Aliases:

 G(gamma)13, h2-35

Location:

 Chr.16:798041-800733 on Build GRCh38

Assay Gene Location:

 Overlaps - Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
GNG13 NM_016541.2 NP_057625.1
AB030207.1 BAA92768.1
AK312139.1
AY029486.1 AAK40269.1
DA111448.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv4828n54 Chr.16:760143 - 828324 on Build GRCh38 Gain MSLN GNG13 PRR25 RPUSD1 CHTF18 MIR662
esv3637582 Chr.16:751057 - 851536 on Build GRCh38 Gain MSLN GNG13 PRR25 RPUSD1 CHTF18 MIR662
esv2422427 Chr.16:10001 - 2723164 on Build GRCh38 Duplication LUC7L LOC107987233 MIR3176 HAGH LOC729652 RHBDL1 NTN3 SSTR5 EME2 LINC00254 FLJ42627 MIR4516 TPSG1 SNHG9 SNRNP25 KCTD5 LOC652276 TSC2 HBA1 RPL3L TBL3 MRPL28 AMDHD2 PDPK1 LMF1-AS1 PRR35 TPSD1 IFT140 DDX11L10 C16orf59 PRR25 BAIAP3 MAPK8IP3 TPSB2 RAB11FIP3 CASKIN1 PKD1 NME3 AXIN1 STUB1 TSR3 PDIA2 MEIOB RAB40C ERVK13-1 MIR6859-4 LOC106660606 PIGQ WDR24 SNORA10 TMEM8A FAHD1 LOC105371049 LOC100134368 NPRL3 ZNF598 LOC105371047 ARHGDIG MIR4717 CRAMP1 LOC105371045 LINC00235 ABCA17P LOC105371046 HBQ1 NTHL1 NHLRC4 METRN GNPTG MIR3177 SNORD60 UNKL FBXL16 CCDC154 MIR940 MIR5587 MIR3178 RGS11 CHTF18 NARFL RPS2 CAPN15 BRICD5 TELO2 C1QTNF8 RNPS1 MIR3677 TMEM204 CEMP1 SNORA78 HBZ RPL23AP5 SLC9A3R2 WFIKKN1 MIR1225 IGFALS JMJD8 PGP WASIR2 C16orf91 MPG FAM173A METTL26 LOC105371038 RNF151 ATP6V0C MIR6768 CACNA1H NME4 TRAF7 RAB26 HAGHL MIR6511B1 UBE2I WDR90 HN1L RPUSD1 NDUFB10 MLST8 CCDC78 NUBP2 SNORA64 MIR662 SNHG19 CLCN7 TBC1D24 MRPS34 SPSB3 PRSS29P HBM SOX8 RHOT2 MSRB1 MCRIP2 RHBDF1 LOC101929280 LOC105371184 LOC107984876 DNASE1L2 MSLN CCNF FAM234A DECR2 NOXO1 ABCA3 ECI1 TPSAB1 GFER MIR3180-5 MIR6767 E4F1 LMF1 SYNGR3 GNG13 POLR3K HBA2 LOC100287175 HS3ST6 PTX4 PRSS27 NPW SSTR5-AS1
nsv471063 Chr.16:520623 - 852322 on Build GRCh38 Loss RAB40C WDR90 WFIKKN1 LOC107987233 RPUSD1 MIR3176 PIGQ WDR24 RHBDL1 JMJD8 CCDC78 MIR662 LINC00235 NHLRC4 METRN FAM173A RHOT2 MCRIP2 METTL26 LOC101929280 LOC105371184 MSLN LOC105371038 PRR35 FBXL16 MIR5587 CHTF18 NARFL CAPN15 GNG13 PRR25 LOC100287175 RAB11FIP3 STUB1 HAGHL
nsv526903 Chr.16:451362 - 810673 on Build GRCh38 Loss RAB40C WDR90 WFIKKN1 LOC107987233 RPUSD1 MIR3176 PIGQ WDR24 RHBDL1 JMJD8 CCDC78 MIR662 LINC00235 NHLRC4 METRN FAM173A RHOT2 MCRIP2 METTL26 LOC101929280 LOC105371184 MSLN LOC105371038 PRR35 FBXL16 MIR5587 CHTF18 NARFL CAPN15 GNG13 PRR25 LOC100287175 RAB11FIP3 STUB1 HAGHL
esv3570042 Chr.16:793849 - 822928 on Build GRCh38 Gain GNG13 PRR25 CHTF18
nsv952898 Chr.16:495001 - 1132900 on Build GRCh38 Deletion RAB40C WDR90 WFIKKN1 LOC107987233 RPUSD1 MIR3176 PIGQ WDR24 RHBDL1 JMJD8 SSTR5 CCDC78 MIR662 LINC00235 NHLRC4 METRN SOX8 FAM173A RHOT2 MCRIP2 METTL26 LOC101929280 LOC105371184 LOC107984876 MSLN LMF1-AS1 LOC105371038 PRR35 FBXL16 MIR5587 CHTF18 NARFL LMF1 CAPN15 GNG13 PRR25 C1QTNF8 LOC100287175 RAB11FIP3 STUB1 HAGHL SSTR5-AS1
nsv571042 Chr.16:785298 - 847566 on Build GRCh38 Loss GNG13 PRR25 RPUSD1 CHTF18
nsv482184 Chr.16:798041 - 800733 on Build GRCh38 Gain GNG13 CHTF18
nsv1160326 Chr.16:580902 - 804689 on Build GRCh38 Duplication RAB40C WDR90 WFIKKN1 RPUSD1 PIGQ WDR24 RHBDL1 JMJD8 CCDC78 MIR662 METRN FAM173A RHOT2 MCRIP2 METTL26 LOC101929280 LOC105371184 MSLN LOC105371038 FBXL16 CHTF18 NARFL GNG13 LOC100287175 STUB1 HAGHL
esv3637584 Chr.16:798001 - 812299 on Build GRCh38 Loss GNG13 PRR25 CHTF18
nsv1160325 Chr.16:506925 - 836376 on Build GRCh38 Duplication RAB40C WDR90 WFIKKN1 LOC107987233 RPUSD1 MIR3176 PIGQ WDR24 RHBDL1 JMJD8 CCDC78 MIR662 LINC00235 NHLRC4 METRN FAM173A RHOT2 MCRIP2 METTL26 LOC101929280 LOC105371184 MSLN LOC105371038 PRR35 FBXL16 MIR5587 CHTF18 NARFL CAPN15 GNG13 PRR25 LOC100287175 RAB11FIP3 STUB1 HAGHL
nsv817712 Chr.16:774098 - 810673 on Build GRCh38 Loss GNG13 PRR25 RPUSD1 CHTF18
esv3637587 Chr.16:798995 - 892120 on Build GRCh38 Gain LMF1 GNG13 PRR25
nsv9321 Chr.16:638149 - 804328 on Build GRCh38 Gain+Loss WDR90 LOC105371184 MSLN LOC105371038 RPUSD1 WDR24 FBXL16 RHBDL1 JMJD8 CCDC78 CHTF18 NARFL MIR662 GNG13 LOC100287175 METRN STUB1 FAM173A HAGHL RHOT2 MCRIP2
nsv571045 Chr.16:790597 - 847566 on Build GRCh38 Gain GNG13 PRR25 CHTF18
nsv517488 Chr.16:760039 - 810673 on Build GRCh38 Loss MSLN GNG13 PRR25 RPUSD1 CHTF18 MIR662
esv3637588 Chr.16:799071 - 846677 on Build GRCh38 Loss GNG13 PRR25

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More Information


Additional Information:

For this assay, SNP(s) [rs78987137] 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 Non-exonic DGV Variation

Panther Classification:

Molecular Function -

heterotrimeric G-protein

Gene Ontology Categories:

Function(s) Process(es)


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