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