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 5 - Intron 6 |
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 | |||
AB209582.1 | 1 | 742 | BAD92819.1 | |
AF035153.1 | AAC69175.1 | |||
AF035154.1 | AAC69176.1 | |||
AK091701.1 | ||||
AK293564.1 | ||||
AK294448.1 | ||||
AK308972.1 | ||||
BC040504.1 | AAH40504.1 | |||
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 | SSTR5-AS1 TPSG1 LOC105371045 RPL23AP5 PIGQ GNPTG ZNF598 NHLRC4 LMF1-AS1 TSR3 MIR6768 SPSB3 LUC7L CAPN15 NUBP2 RAB40C LOC100134368 MLST8 RHOT2 TPSB2 CCDC78 HBQ1 MIR4516 MIR3176 SNHG19 MIR6859-4 RPL3L AXIN1 PKD1 MIR3177 NME3 CASKIN1 GFER EME2 SYNGR3 METTL26 LOC107987233 MSLN MPG MIR6511B1 FAHD1 FAM234A PRR35 STUB1 TMEM204 JMJD8 MIR940 TBC1D24 TBL3 NPRL3 ERVK13-1 METRN NTN3 FBXL16 ABCA3 WASIR2 NPW LOC107984876 NME4 PRSS29P SNORA10 SSTR5 LOC105371046 SLC9A3R2 LOC105371049 TRAF7 CHTF18 MIR3178 MIR4717 RHBDL1 MSRB1 BAIAP3 CLCN7 WFIKKN1 RNPS1 ABCA17P HAGHL RAB11FIP3 LINC00254 HS3ST6 SNORD60 RPS2 ECI1 NDUFB10 SNORA78 SNORA64 PTX4 PRSS27 MIR1225 RAB26 FLJ42627 FAM173A UNKL E4F1 POLR3K ARHGDIG MCRIP2 PDIA2 DDX11L10 IGFALS HBA2 HBZ CCDC154 RNF151 HBM BRICD5 TPSD1 DNASE1L2 MEIOB CCNF C1QTNF8 KCTD5 AMDHD2 HBA1 HAGH LMF1 HN1L MIR5587 LOC105371184 LOC105371038 MIR3677 MRPL28 WDR24 LOC652276 LOC101929280 MIR662 CACNA1H RGS11 LOC105371047 LINC00235 TELO2 NARFL GNG13 MRPS34 UBE2I NTHL1 MIR6767 C16orf91 TPSAB1 WDR90 MIR3180-5 PGP PRR25 PDPK1 CEMP1 TSC2 SNRNP25 LOC729652 RHBDF1 TMEM8A LOC100287175 CRAMP1 SNHG9 DECR2 IFT140 MAPK8IP3 ATP6V0C SOX8 LOC106660606 NOXO1 RPUSD1 C16orf59 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | FAM234A RGS11 |
nsv952896 | Chr.16:273501 - 321500 on Build GRCh38 | Deletion | AXIN1 ARHGDIG PDIA2 RGS11 |
esv3637563 | Chr.16:263248 - 505590 on Build GRCh38 | Gain | RPL23AP5 DECR2 LOC100134368 TMEM8A AXIN1 ARHGDIG RAB11FIP3 PDIA2 MRPL28 NME4 FAM234A RGS11 |
nsv827477 | Chr.16:262247 - 297639 on Build GRCh38 | Gain | AXIN1 ARHGDIG PDIA2 FAM234A RGS11 |
nsv570947 | Chr.16:272935 - 297326 on Build GRCh38 | Loss | AXIN1 ARHGDIG PDIA2 RGS11 |
dgv32n68 | Chr.16:245507 - 476226 on Build GRCh38 | Loss | RPL23AP5 DECR2 LOC100134368 TMEM8A AXIN1 ARHGDIG RAB11FIP3 PDIA2 MRPL28 NME4 FAM234A RGS11 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |