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 6 - Intron 7 |
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 | BAD92819.1 | |||
AF035153.1 | AAC69175.1 | |||
AF035154.1 | AAC69176.1 | |||
AK091701.1 | ||||
AK293564.1 | ||||
AK294448.1 | ||||
AK308972.1 | ||||
BC040504.1 | AAH40504.1 | |||
BC141803.1 | ||||
EF212269.1 |
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 | DDX11L10 MIR4717 C16orf91 RHBDL1 PTX4 ECI1 MIR3180-5 MIR5587 SPSB3 POLR3K ERVK13-1 PDPK1 GNPTG TMEM8A HBA2 PRR25 ZNF598 GNG13 SNHG19 RNF151 LOC105371184 MAPK8IP3 CACNA1H PGP CCDC78 HBA1 LOC107987233 ARHGDIG MSLN SSTR5-AS1 NTN3 DNASE1L2 TSR3 WFIKKN1 LOC106660606 MIR3176 WDR24 ATP6V0C NPW WDR90 MEIOB UBE2I LMF1 DECR2 RGS11 PDIA2 CRAMP1 LOC105371045 CCNF C16orf59 RPS2 BRICD5 FAM173A HBM PRSS27 SNORA64 MIR662 BAIAP3 HS3ST6 MCRIP2 SNORA78 CCDC154 RHBDF1 MIR6767 SSTR5 SYNGR3 TMEM204 WASIR2 SNHG9 LUC7L RNPS1 SNORA10 RHOT2 CAPN15 TBC1D24 MSRB1 CHTF18 RPL3L HAGHL MIR3178 PRSS29P LOC105371046 LOC100287175 RPL23AP5 SLC9A3R2 LMF1-AS1 HAGH ABCA3 RAB40C NME3 AXIN1 TPSG1 LINC00235 CEMP1 TSC2 HBZ IFT140 LOC107984876 LOC729652 PIGQ MRPL28 PRR35 TRAF7 NHLRC4 TPSAB1 METTL26 TELO2 NUBP2 C1QTNF8 CASKIN1 RAB26 SNORD60 PKD1 MPG LOC105371049 HBQ1 UNKL TPSD1 NARFL STUB1 ABCA17P FAM234A LOC652276 TBL3 E4F1 MIR1225 HN1L TPSB2 KCTD5 AMDHD2 EME2 IGFALS CLCN7 JMJD8 MLST8 MIR940 LOC105371038 MIR4516 NPRL3 MIR3677 FBXL16 LOC101929280 FAHD1 SNRNP25 NDUFB10 MIR6511B1 MIR6768 LOC105371047 SOX8 MIR3177 LOC100134368 FLJ42627 MRPS34 LINC00254 RAB11FIP3 GFER NOXO1 MIR6859-4 METRN NME4 RPUSD1 NTHL1 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | FAM234A RGS11 |
nsv952896 | Chr.16:273501 - 321500 on Build GRCh38 | Deletion | AXIN1 ARHGDIG RGS11 PDIA2 |
esv3637563 | Chr.16:263248 - 505590 on Build GRCh38 | Gain | LOC100134368 RAB11FIP3 MRPL28 AXIN1 ARHGDIG FAM234A NME4 RPL23AP5 DECR2 RGS11 PDIA2 TMEM8A |
nsv827477 | Chr.16:262247 - 297639 on Build GRCh38 | Gain | AXIN1 ARHGDIG FAM234A RGS11 PDIA2 |
nsv570947 | Chr.16:272935 - 297326 on Build GRCh38 | Loss | AXIN1 ARHGDIG RGS11 PDIA2 |
dgv32n68 | Chr.16:245507 - 476226 on Build GRCh38 | Loss | LOC100134368 RAB11FIP3 MRPL28 AXIN1 ARHGDIG FAM234A NME4 RPL23AP5 DECR2 RGS11 PDIA2 TMEM8A |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |