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 RGS11 CNV Assays ›
Gene Symbol
RGS11
Assay Reference Genome
Location

Chr.16:270798 on build GRCh38
Cytoband
16p13.3
Assay ID Hs01886315_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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 16 - Intron 17
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
AB016929.1 BAA74751.1
AB209582.1 BAD92819.1
AF035153.1 AAC69175.1
AF035154.1 AAC69176.1
AK091701.1
AK293564.1
BC141803.1

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 SNORA64 TBL3 CCNF LOC105371046 HAGHL WDR24 LOC100287175 LOC101929280 KCTD5 GNG13 MRPS34 WASIR2 FAHD1 LINC00254 TELO2 RAB26 FLJ42627 SSTR5-AS1 TBC1D24 C16orf91 MIR3176 PRR35 E4F1 RAB11FIP3 UBE2I NME3 MIR4516 POLR3K GFER ATP6V0C SNHG9 MRPL28 BAIAP3 HAGH MIR1225 SNORD60 TPSG1 RPS2 HBM NPW NUBP2 C16orf59 ABCA3 LOC105371047 BRICD5 LOC106660606 SNORA78 METRN CHTF18 HS3ST6 LOC105371049 CCDC78 SLC9A3R2 UNKL SPSB3 SNRNP25 ECI1 RNF151 WDR90 CCDC154 LMF1 STUB1 PRSS27 TSC2 NPRL3 PTX4 MLST8 HBQ1 LOC105371045 AMDHD2 PGP LOC652276 LINC00235 LOC107984876 ABCA17P PRSS29P CASKIN1 LOC105371184 DDX11L10 TRAF7 TMEM8A ERVK13-1 PKD1 MIR6768 MIR662 CRAMP1 MIR6767 SNHG19 MSRB1 SOX8 RHOT2 CEMP1 HBA2 MIR4717 LOC107987233 MCRIP2 MIR3677 DNASE1L2 JMJD8 RNPS1 HBZ FAM234A WFIKKN1 RPUSD1 IGFALS RPL23AP5 NTN3 RAB40C FBXL16 PRR25 SNORA10 TSR3 TPSAB1 MIR6859-4 NARFL MIR5587 ZNF598 RGS11 NDUFB10 MIR3180-5 MEIOB TMEM204 SSTR5 MSLN LOC100134368 MIR940 C1QTNF8 HN1L MPG RPL3L TPSD1 MIR3177 PDPK1 ARHGDIG RHBDL1 NOXO1 HBA1 METTL26 MAPK8IP3 CAPN15 NHLRC4 CLCN7 FAM173A SYNGR3 CACNA1H AXIN1 EME2 MIR6511B1 LOC729652 GNPTG IFT140 PDIA2 TPSB2 DECR2 PIGQ NME4 RHBDF1 NTHL1 LOC105371038 LMF1-AS1 LUC7L MIR3178
esv3570031 Chr.16:243389 - 278107 on Build GRCh38 Gain RGS11 FAM234A
esv3637563 Chr.16:263248 - 505590 on Build GRCh38 Gain RAB11FIP3 TMEM8A RGS11 AXIN1 LOC100134368 RPL23AP5 MRPL28 PDIA2 DECR2 NME4 ARHGDIG FAM234A
nsv827477 Chr.16:262247 - 297639 on Build GRCh38 Gain RGS11 AXIN1 PDIA2 ARHGDIG FAM234A
esv3637561 Chr.16:261769 - 271795 on Build GRCh38 Loss RGS11 FAM234A
dgv32n68 Chr.16:245507 - 476226 on Build GRCh38 Loss RAB11FIP3 TMEM8A RGS11 AXIN1 LOC100134368 RPL23AP5 MRPL28 PDIA2 DECR2 NME4 ARHGDIG FAM234A

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs74988319] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products