Hs01890913_cn

• Gene Symbol: GNG13
• Assay Reference Genome Location: Chr.16:799035 on build GRCh38
• Cytoband: 16p13.3

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: Within Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
GNG13	NM_016541.2	2	145	NP_057625.1
	AB030207.1	2	124	BAA92768.1
	AF493880.1	1	43	AAM12594.1
	AK312139.1	2	146
	AY029486.1	2	111	AAK40269.1
	BC093760.1	1	76	AAH93760.1
	BC095525.1	1	46	AAH95525.1
	DA111448.1	2	146

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

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

heterotrimeric G-protein

Gene Ontology Categories:

Process(es)

phospholipase C-activating G-protein coupled receptor signaling pathway
sensory perception of taste
cellular response to glucagon stimulus

Function(s)

signal transducer activity
G-protein beta-subunit binding