Assay Details
Target Gene Details
Entrez Gene ID: | 83986 |
Gene Name: | family with sequence similarity 234 member A |
Gene Aliases: |
C16orf9, ITFG3, gs19 |
Location: |
Chr.16:234546-269943 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM234A | NM_001284497.1 | NP_001271426.1 | ||
NM_032039.3 | NP_114428.1 | |||
NR_104317.1 | ||||
XM_005255622.1 | XP_005255679.1 | |||
XM_005255623.2 | XP_005255680.1 | |||
XM_006720957.1 | XP_006721020.1 | |||
XM_011522691.1 | XP_011520993.1 | |||
XM_011522692.1 | XP_011520994.1 | |||
XM_017023760.1 | XP_016879249.1 | |||
XM_017023761.1 | XP_016879250.1 | |||
XM_017023762.1 | XP_016879251.1 | |||
XM_017023763.1 | XP_016879252.1 | |||
XM_017023764.1 | XP_016879253.1 | |||
XM_017023765.1 | XP_016879254.1 | |||
AK057165.1 | BAB71374.1 | |||
AK294581.1 | ||||
AK310766.1 | ||||
AL136542.1 | CAB66477.1 | |||
BC013047.1 | AAH13047.1 | |||
BC032112.2 | AAH32112.1 | |||
CN262982.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv518291 | Chr.16:47354 - 254515 on Build GRCh38 | Loss | RHBDF1 HBQ1 HBM HBA2 POLR3K SNRNP25 LUC7L NPRL3 FAM234A HBZ MPG HBA1 |
esv2422427 | Chr.16:10001 - 2723164 on Build GRCh38 | Duplication | SNORA78 RPS2 PGP ERVK13-1 RNF151 METRN E4F1 ZNF598 SNORD60 ABCA3 LOC652276 PRSS29P HN1L LINC00254 NUBP2 MIR5587 MIR3177 BRICD5 PDPK1 IGFALS CLCN7 ABCA17P RHBDF1 IFT140 HBM SPSB3 LOC106660606 MIR3176 NTN3 ARHGDIG METTL26 PRSS27 MLST8 SLC9A3R2 HBA1 FAM173A LOC107984876 GNG13 NPRL3 NME4 WDR24 MSRB1 LMF1-AS1 CASKIN1 LOC100134368 DECR2 UBE2I SNRNP25 LMF1 TMEM8A ECI1 ATP6V0C RNPS1 NME3 RPL3L TRAF7 MEIOB TBC1D24 RAB11FIP3 MIR6859-4 LOC105371046 HAGH TELO2 MIR6511B1 STUB1 MPG SOX8 WFIKKN1 CCDC78 LOC101929280 MIR940 LOC105371047 DNASE1L2 CCDC154 C16orf91 SNORA64 TBL3 RPL23AP5 HBQ1 PRR25 RHBDL1 LOC105371184 MIR3180-5 SNORA10 CHTF18 MIR4717 MIR3178 MIR1225 CACNA1H SNHG9 TPSD1 WDR90 FAHD1 LUC7L KCTD5 MRPS34 RAB40C HBZ GFER LOC729652 NTHL1 TPSB2 PRR35 MRPL28 WASIR2 JMJD8 MIR3677 DDX11L10 TMEM204 NARFL RAB26 MIR662 LOC107987233 MCRIP2 PTX4 RGS11 PDIA2 TSR3 MIR6767 RPUSD1 LOC100287175 HBA2 CEMP1 UNKL RHOT2 HS3ST6 FLJ42627 NDUFB10 LINC00235 MSLN SSTR5 SNHG19 MIR4516 LOC105371038 NPW TPSAB1 LOC105371045 POLR3K AMDHD2 CCNF SYNGR3 PIGQ LOC105371049 GNPTG SSTR5-AS1 FBXL16 C16orf59 NOXO1 C1QTNF8 HAGHL CAPN15 TSC2 TPSG1 NHLRC4 CRAMP1 AXIN1 PKD1 FAM234A BAIAP3 MIR6768 EME2 MAPK8IP3 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | FAM234A RGS11 |
nsv1044142 | Chr.16:10765 - 255644 on Build GRCh38 | Gain | HBQ1 HBA2 MIR6859-4 POLR3K SNRNP25 WASIR2 DDX11L10 MPG HBA1 RHBDF1 HBM LUC7L NPRL3 FAM234A HBZ |
dgv32n68 | Chr.16:245507 - 476226 on Build GRCh38 | Loss | RPL23AP5 DECR2 AXIN1 TMEM8A MRPL28 NME4 FAM234A RGS11 PDIA2 ARHGDIG LOC100134368 RAB11FIP3 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |