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See other RGS11 CNV Assays ›
Gene Symbol
RGS11
Assay Reference Genome
Location

Chr.16:275311 on build GRCh38
Cytoband
16p13.3
Assay ID Hs02360412_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 8786

Gene Name:

 regulator of G-protein signaling 11

Gene Aliases:

 RS11

Location:

 Chr.16:268301-275943 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 2 - Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RGS11 NM_001286485.1 NP_001273414.1
NM_001286486.1 NP_001273415.1
NM_003834.2 NP_003825.1
NM_183337.2 NP_899180.1
XM_011522719.2 XP_011521021.1
XM_011522720.2 XP_011521022.1
XM_011522721.1 XP_011521023.1
XM_011522722.1 XP_011521024.1
XM_011522723.1 XP_011521025.1
AB016929.1 BAA74751.1
AF035153.1 AAC69175.1
AF035154.1 AAC69176.1
AK091701.1
AK293564.1
AK294033.1
AK294448.1
AK308972.1
BC040504.1 AAH40504.1
BC141803.1
DC423811.1 2 285

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2422427 Chr.16:10001 - 2723164 on Build GRCh38 Duplication PKD1 UBE2I LOC729652 MLST8 LOC105371038 RGS11 TRAF7 GNG13 NME4 AMDHD2 TPSAB1 FBXL16 C1QTNF8 RHOT2 HAGHL POLR3K MIR3178 LOC652276 AXIN1 CAPN15 MIR662 FAM234A RAB40C JMJD8 MIR6768 C16orf59 MSLN PIGQ STUB1 ZNF598 LOC106660606 MIR940 RPUSD1 WDR24 TMEM204 MIR4717 SNORD60 SSTR5-AS1 HS3ST6 CASKIN1 TMEM8A FLJ42627 LMF1 ECI1 NTHL1 TPSG1 MIR6859-4 WDR90 LOC107984876 KCTD5 PRSS27 MEIOB RHBDF1 WFIKKN1 NARFL NPW MRPL28 SNORA78 PRR35 TPSB2 SOX8 IFT140 NOXO1 SNRNP25 RNPS1 ERVK13-1 C16orf91 RAB11FIP3 TSR3 SLC9A3R2 ABCA3 SNORA10 MCRIP2 NDUFB10 RNF151 LOC105371047 FAHD1 LUC7L WASIR2 SNORA64 NPRL3 HN1L CHTF18 DECR2 NUBP2 EME2 HAGH PRSS29P SPSB3 PRR25 HBA1 ABCA17P MPG BRICD5 RPL3L SNHG19 MAPK8IP3 HBZ TBL3 MIR3176 PTX4 MIR3177 LOC105371046 GFER MIR3677 LOC105371184 LINC00235 RAB26 PDPK1 CLCN7 MIR1225 LINC00254 TELO2 E4F1 LOC100134368 RPS2 LOC101929280 NHLRC4 SYNGR3 HBQ1 MIR6511B1 METTL26 CACNA1H GNPTG IGFALS LOC100287175 UNKL MRPS34 PDIA2 CCDC154 CCDC78 HBM MSRB1 LOC105371045 MIR6767 DNASE1L2 RPL23AP5 HBA2 LMF1-AS1 SNHG9 FAM173A LOC107987233 TPSD1 NME3 ATP6V0C CEMP1 CRAMP1 BAIAP3 SSTR5 TSC2 MIR5587 PGP LOC105371049 RHBDL1 TBC1D24 METRN ARHGDIG MIR4516 MIR3180-5 NTN3 DDX11L10 CCNF
esv3570031 Chr.16:243389 - 278107 on Build GRCh38 Gain RGS11 FAM234A
nsv952896 Chr.16:273501 - 321500 on Build GRCh38 Deletion PDIA2 ARHGDIG RGS11 AXIN1
esv3637563 Chr.16:263248 - 505590 on Build GRCh38 Gain PDIA2 RAB11FIP3 NME4 TMEM8A ARHGDIG MRPL28 RGS11 LOC100134368 DECR2 RPL23AP5 AXIN1 FAM234A
nsv827477 Chr.16:262247 - 297639 on Build GRCh38 Gain PDIA2 ARHGDIG RGS11 AXIN1 FAM234A
nsv570947 Chr.16:272935 - 297326 on Build GRCh38 Loss PDIA2 ARHGDIG RGS11 AXIN1
dgv32n68 Chr.16:245507 - 476226 on Build GRCh38 Loss PDIA2 RAB11FIP3 NME4 TMEM8A ARHGDIG MRPL28 RGS11 LOC100134368 DECR2 RPL23AP5 AXIN1 FAM234A

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More Information


Additional Information:

For this assay, SNP(s) [rs117215141] 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

Gene Ontology Categories:

Function(s) Process(es)


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