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 POLR3K HBM FAM234A NPRL3 MPG RHBDF1 LUC7L HBQ1 HBZ HBA2 HBA1 |
esv2422427 | Chr.16:10001 - 2723164 on Build GRCh38 | Duplication | SNRNP25 SSTR5 GFER MIR3180-5 LOC107987233 LOC105371184 RNPS1 LOC105371049 TRAF7 LOC107984876 MIR6767 SSTR5-AS1 C16orf59 PDIA2 NARFL RPL3L LOC100134368 MAPK8IP3 SNORA78 GNG13 MIR1225 SPSB3 TSC2 ATP6V0C PDPK1 CHTF18 AXIN1 LOC652276 FAM234A JMJD8 ECI1 RAB40C NME4 NUBP2 UBE2I ERVK13-1 CASKIN1 HBQ1 E4F1 MIR940 NOXO1 CCNF PRSS29P RPUSD1 TPSG1 NTHL1 FAM173A MIR6511B1 SNHG19 UNKL TELO2 PRR25 LOC100287175 STUB1 MEIOB MIR3176 HS3ST6 SNORA64 TMEM8A C16orf91 NME3 ARHGDIG MRPL28 TPSD1 LOC105371038 POLR3K PKD1 LOC105371045 DDX11L10 RAB26 CLCN7 LMF1-AS1 TMEM204 NHLRC4 TBL3 HBZ SNORA10 MSLN MIR6859-4 LINC00254 AMDHD2 BAIAP3 WDR90 SOX8 LOC105371046 RHBDL1 KCTD5 MRPS34 RHOT2 LMF1 CRAMP1 LOC729652 NDUFB10 SYNGR3 TPSAB1 PIGQ GNPTG PRR35 MIR4717 MIR3677 PGP LINC00235 PRSS27 LOC105371047 EME2 RNF151 MIR4516 WFIKKN1 CACNA1H ABCA3 MPG CCDC154 IGFALS MLST8 SNORD60 FBXL16 HN1L FAHD1 C1QTNF8 HAGHL PTX4 DNASE1L2 METRN MIR662 MCRIP2 LUC7L LOC101929280 FLJ42627 MIR3178 ABCA17P CAPN15 TBC1D24 RGS11 NPRL3 CCDC78 LOC106660606 RPL23AP5 TPSB2 RHBDF1 IFT140 TSR3 METTL26 NTN3 CEMP1 MSRB1 HBM WDR24 MIR6768 MIR3177 NPW HBA2 HBA1 SLC9A3R2 RAB11FIP3 ZNF598 DECR2 HAGH SNHG9 BRICD5 MIR5587 WASIR2 RPS2 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | FAM234A RGS11 |
nsv1044142 | Chr.16:10765 - 255644 on Build GRCh38 | Gain | SNRNP25 POLR3K HBM DDX11L10 FAM234A MPG LUC7L HBZ MIR6859-4 HBA2 HBA1 NPRL3 RHBDF1 HBQ1 WASIR2 |
esv2660459 | Chr.16:244784 - 246872 on Build GRCh38 | Deletion | FAM234A |
dgv32n68 | Chr.16:245507 - 476226 on Build GRCh38 | Loss | PDIA2 MRPL28 AXIN1 RAB11FIP3 DECR2 LOC100134368 FAM234A RGS11 RPL23AP5 TMEM8A NME4 ARHGDIG |
esv3637559 | Chr.16:244840 - 246974 on Build GRCh38 | Loss | FAM234A |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |