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: | Overlaps Intron 14 - Exon 15 |
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 | ||||
AL136542.1 | CAB66477.1 | |||
BC010521.1 | AAH10521.1 | |||
BC013047.1 | AAH13047.1 | |||
BC032112.2 | AAH32112.1 |
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 | TPSD1 RHOT2 HAGHL MIR6859-4 KCTD5 LOC105371045 FAM173A LOC105371038 METTL26 SOX8 HS3ST6 E4F1 CRAMP1 MAPK8IP3 RNPS1 ABCA17P TPSG1 WASIR2 HN1L BRICD5 FLJ42627 LOC652276 PGP FAHD1 RAB40C WDR24 TMEM8A FBXL16 CAPN15 ABCA3 CCNF SNHG19 PRR35 NPW MLST8 MIR4717 NPRL3 SSTR5 UBE2I CEMP1 TRAF7 C1QTNF8 DNASE1L2 LOC100134368 NOXO1 SYNGR3 PTX4 MIR3178 RGS11 CASKIN1 BAIAP3 LOC105371049 RHBDF1 HBA2 MCRIP2 RNF151 PRR25 WDR90 MIR3677 HAGH NHLRC4 SLC9A3R2 LUC7L ARHGDIG LOC100287175 TPSAB1 CLCN7 RAB26 POLR3K DDX11L10 HBQ1 MIR662 LOC101929280 CACNA1H TBL3 NDUFB10 RPL3L CCDC78 SPSB3 LINC00235 GFER LOC107984876 MRPL28 FAM234A MEIOB LMF1 SSTR5-AS1 MIR3180-5 PRSS27 TSC2 WFIKKN1 ECI1 IFT140 SNORA78 TELO2 CHTF18 DECR2 NUBP2 MRPS34 NTHL1 LOC106660606 MIR6767 RHBDL1 MIR5587 LMF1-AS1 TBC1D24 TMEM204 ZNF598 NME3 TPSB2 AMDHD2 MIR940 RPUSD1 AXIN1 PDPK1 ERVK13-1 HBM MIR1225 IGFALS MIR4516 UNKL RAB11FIP3 LOC107987233 ATP6V0C SNORA10 GNG13 MPG MIR6768 EME2 HBZ LOC729652 LOC105371184 MIR3176 NARFL TSR3 SNRNP25 LOC105371047 MSLN LOC105371046 SNHG9 C16orf91 PIGQ C16orf59 RPS2 CCDC154 PDIA2 SNORA64 PRSS29P GNPTG METRN PKD1 NME4 SNORD60 MIR3177 MIR6511B1 NTN3 MSRB1 HBA1 LINC00254 STUB1 RPL23AP5 JMJD8 |
esv3570031 | Chr.16:243389 - 278107 on Build GRCh38 | Gain | FAM234A RGS11 |
esv3637563 | Chr.16:263248 - 505590 on Build GRCh38 | Gain | MRPL28 LOC100134368 FAM234A RAB11FIP3 DECR2 RGS11 AXIN1 PDIA2 RPL23AP5 NME4 TMEM8A ARHGDIG |
nsv827477 | Chr.16:262247 - 297639 on Build GRCh38 | Gain | FAM234A RGS11 AXIN1 PDIA2 ARHGDIG |
esv3637561 | Chr.16:261769 - 271795 on Build GRCh38 | Loss | FAM234A RGS11 |
dgv32n68 | Chr.16:245507 - 476226 on Build GRCh38 | Loss | MRPL28 LOC100134368 FAM234A RAB11FIP3 DECR2 RGS11 AXIN1 PDIA2 RPL23AP5 NME4 TMEM8A ARHGDIG |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |