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 3 |
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 | |||
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 | SNRNP25 HBZ LUC7L POLR3K HBQ1 HBA2 FAM234A HBA1 MPG RHBDF1 HBM NPRL3 |
esv2422427 | Chr.16:10001 - 2723164 on Build GRCh38 | Duplication | LINC00254 IGFALS LOC105371184 MRPL28 BAIAP3 HAGH PRSS29P CCNF MIR3176 SNORD60 PRR35 RHOT2 METRN MIR3178 LOC100287175 MIR1225 LUC7L PRSS27 ATP6V0C CCDC78 RAB26 C1QTNF8 LOC652276 NHLRC4 KCTD5 SSTR5-AS1 FBXL16 HN1L RPL3L FLJ42627 WDR24 PTX4 PKD1 LMF1-AS1 BRICD5 MIR4717 NPRL3 DNASE1L2 MIR3180-5 NARFL RAB11FIP3 LOC105371046 GNG13 GFER TELO2 MIR940 LOC101929280 POLR3K LOC105371047 NME3 HBA1 RPS2 MPG LOC107987233 UNKL RHBDL1 ABCA17P SOX8 SNRNP25 MIR5587 PGP SYNGR3 TPSB2 LOC106660606 LOC105371049 SNORA10 NTN3 MIR6767 FAHD1 MSLN SLC9A3R2 EME2 NOXO1 WFIKKN1 RPUSD1 TMEM204 TBL3 JMJD8 MIR662 PRR25 MEIOB LMF1 MIR6768 ARHGDIG HBZ PDIA2 MCRIP2 ZNF598 DDX11L10 CASKIN1 LOC105371038 E4F1 METTL26 WDR90 SPSB3 FAM234A MRPS34 NME4 TRAF7 CACNA1H HAGHL RAB40C HBQ1 ECI1 CLCN7 MIR3177 TSC2 NDUFB10 NUBP2 NTHL1 MIR4516 ERVK13-1 AMDHD2 UBE2I MIR3677 GNPTG LOC105371045 RPL23AP5 TPSD1 CCDC154 CHTF18 RNPS1 PDPK1 MSRB1 HBM LOC100134368 SNHG9 SSTR5 DECR2 RGS11 MAPK8IP3 PIGQ NPW IFT140 FAM173A MLST8 MIR6859-4 RHBDF1 CRAMP1 LINC00235 AXIN1 TBC1D24 WASIR2 STUB1 SNHG19 TMEM8A SNORA64 ABCA3 MIR6511B1 CEMP1 CAPN15 HBA2 HS3ST6 TPSG1 C16orf59 C16orf91 LOC107984876 TPSAB1 SNORA78 LOC729652 TSR3 RNF151 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | RGS11 FAM234A |
nsv1044142 | Chr.16:10765 - 255644 on Build GRCh38 | Gain | SNRNP25 HBZ LUC7L HBQ1 HBA2 MIR6859-4 DDX11L10 RHBDF1 POLR3K WASIR2 FAM234A HBA1 MPG HBM NPRL3 |
esv2660459 | Chr.16:244784 - 246872 on Build GRCh38 | Deletion | FAM234A |
esv3637559 | Chr.16:244840 - 246974 on Build GRCh38 | Loss | FAM234A |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |