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	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	GNG13 MSLN CHTF18 RPUSD1 MIR662 PRR25
esv3637582	Chr.16:751057 - 851536 on Build GRCh38	Gain	GNG13 MSLN CHTF18 RPUSD1 MIR662 PRR25
esv2422427	Chr.16:10001 - 2723164 on Build GRCh38	Duplication	LOC729652 MIR5587 NPW WDR90 AXIN1 MIR6511B1 LOC107984876 WASIR2 FAM234A HAGH MIR6768 NARFL MIR6859-4 WDR24 TMEM204 POLR3K SSTR5 ABCA17P LOC105371045 NOXO1 MIR3176 LOC100287175 MIR3180-5 LOC105371184 C16orf59 MIR662 SSTR5-AS1 PDIA2 METRN RAB26 PDPK1 SNHG19 RNF151 PRSS27 TPSD1 TPSG1 KCTD5 STUB1 TBL3 ATP6V0C LOC100134368 MRPS34 IGFALS RPL3L PGP NUBP2 METTL26 RHBDL1 TPSAB1 RHBDF1 CAPN15 MIR3177 AMDHD2 LINC00235 SNORA10 TBC1D24 NPRL3 LOC101929280 MIR1225 EME2 LOC105371049 FBXL16 MIR4516 PRR35 LUC7L TELO2 CCDC154 TMEM8A LMF1-AS1 CEMP1 LOC652276 MAPK8IP3 GNPTG HBZ SOX8 MSLN NME4 RAB40C PRSS29P MIR6767 SNHG9 C16orf91 GFER TPSB2 E4F1 LOC105371038 DDX11L10 TRAF7 SNORD60 PIGQ UBE2I ABCA3 ECI1 MPG LOC105371046 MSRB1 GNG13 FAHD1 PKD1 MCRIP2 FAM173A RHOT2 MLST8 DECR2 RAB11FIP3 CCDC78 TSR3 MIR4717 SNORA78 CHTF18 RPUSD1 DNASE1L2 LMF1 LOC106660606 ERVK13-1 CASKIN1 MRPL28 LINC00254 RNPS1 ARHGDIG HN1L MEIOB RGS11 PTX4 RPS2 LOC107987233 MIR3178 IFT140 HBA1 SPSB3 SLC9A3R2 CRAMP1 BAIAP3 NDUFB10 NME3 C1QTNF8 LOC105371047 BRICD5 NHLRC4 RPL23AP5 FLJ42627 HS3ST6 ZNF598 MIR3677 PRR25 MIR940 SNORA64 CLCN7 HBA2 CCNF HBQ1 NTHL1 HBM SYNGR3 NTN3 WFIKKN1 UNKL JMJD8 TSC2 HAGHL SNRNP25 CACNA1H
nsv471063	Chr.16:520623 - 852322 on Build GRCh38	Loss	LOC107987233 MIR5587 PIGQ WDR90 METTL26 GNG13 RHBDL1 NHLRC4 CAPN15 NARFL MCRIP2 WDR24 FAM173A RHOT2 RAB11FIP3 CCDC78 LINC00235 PRR25 LOC101929280 MIR3176 LOC100287175 CHTF18 LOC105371184 FBXL16 PRR35 RPUSD1 MIR662 METRN MSLN WFIKKN1 RAB40C JMJD8 LOC105371038 HAGHL STUB1
nsv526903	Chr.16:451362 - 810673 on Build GRCh38	Loss	LOC107987233 MIR5587 PIGQ WDR90 METTL26 GNG13 RHBDL1 NHLRC4 CAPN15 NARFL MCRIP2 WDR24 FAM173A RHOT2 RAB11FIP3 CCDC78 LINC00235 PRR25 LOC101929280 MIR3176 LOC100287175 CHTF18 LOC105371184 FBXL16 PRR35 RPUSD1 MIR662 METRN MSLN WFIKKN1 RAB40C JMJD8 LOC105371038 HAGHL STUB1
esv3570042	Chr.16:793849 - 822928 on Build GRCh38	Gain	GNG13 CHTF18 PRR25
nsv952898	Chr.16:495001 - 1132900 on Build GRCh38	Deletion	LOC107987233 MIR5587 PIGQ WDR90 LOC107984876 METTL26 C1QTNF8 GNG13 RHBDL1 NHLRC4 CAPN15 NARFL MCRIP2 WDR24 FAM173A RHOT2 RAB11FIP3 SSTR5 CCDC78 LINC00235 PRR25 LOC101929280 MIR3176 LOC100287175 CHTF18 LOC105371184 FBXL16 PRR35 RPUSD1 MIR662 SSTR5-AS1 LMF1-AS1 METRN LMF1 SOX8 MSLN WFIKKN1 RAB40C JMJD8 LOC105371038 HAGHL STUB1
nsv571042	Chr.16:785298 - 847566 on Build GRCh38	Loss	GNG13 CHTF18 RPUSD1 PRR25
nsv482184	Chr.16:798041 - 800733 on Build GRCh38	Gain	GNG13 CHTF18
esv3637585	Chr.16:798001 - 812299 on Build GRCh38	Gain	GNG13 CHTF18 PRR25
nsv1160326	Chr.16:580902 - 804689 on Build GRCh38	Duplication	PIGQ WDR90 METTL26 GNG13 RHBDL1 NARFL MCRIP2 WDR24 FAM173A RHOT2 CCDC78 LOC101929280 LOC100287175 CHTF18 LOC105371184 FBXL16 RPUSD1 MIR662 METRN MSLN WFIKKN1 RAB40C JMJD8 LOC105371038 HAGHL STUB1
nsv1160325	Chr.16:506925 - 836376 on Build GRCh38	Duplication	LOC107987233 MIR5587 PIGQ WDR90 METTL26 GNG13 RHBDL1 NHLRC4 CAPN15 NARFL MCRIP2 WDR24 FAM173A RHOT2 RAB11FIP3 CCDC78 LINC00235 PRR25 LOC101929280 MIR3176 LOC100287175 CHTF18 LOC105371184 FBXL16 PRR35 RPUSD1 MIR662 METRN MSLN WFIKKN1 RAB40C JMJD8 LOC105371038 HAGHL STUB1
nsv817712	Chr.16:774098 - 810673 on Build GRCh38	Loss	GNG13 CHTF18 RPUSD1 PRR25
esv3637586	Chr.16:798995 - 892120 on Build GRCh38	Loss	GNG13 LMF1 PRR25
nsv9321	Chr.16:638149 - 804328 on Build GRCh38	Gain+Loss	LOC100287175 CHTF18 LOC105371184 FBXL16 RPUSD1 WDR90 MIR662 METRN GNG13 MSLN RHBDL1 NARFL MCRIP2 WDR24 FAM173A RHOT2 JMJD8 LOC105371038 CCDC78 HAGHL STUB1
nsv571045	Chr.16:790597 - 847566 on Build GRCh38	Gain	GNG13 CHTF18 PRR25
dgv4827n54	Chr.16:760039 - 810673 on Build GRCh38	Loss	GNG13 MSLN CHTF18 RPUSD1 MIR662 PRR25
esv3637588	Chr.16:799071 - 846677 on Build GRCh38	Loss	GNG13 PRR25

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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System Message

Genomic Map

Assay Details

Target Gene Details

Entrez Gene ID:

Gene Name:

Gene Aliases:

Location:

Assay Gene Location: