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See other FAM234A CNV Assays ›
Gene Symbol
FAM234A
Assay Reference Genome
Location

Chr.16:249644 on build GRCh38
Cytoband
16p13.3
Assay ID Hs01833470_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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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 Exon 5 - 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 POLR3K HBA1 HBZ HBA2 RHBDF1 HBM MPG NPRL3 SNRNP25 LUC7L HBQ1 FAM234A
esv2422427 Chr.16:10001 - 2723164 on Build GRCh38 Duplication MSRB1 CCNF NME3 CEMP1 GFER CHTF18 FLJ42627 SNHG19 RPS2 LINC00235 TELO2 ARHGDIG DNASE1L2 MIR4516 MIR3177 BRICD5 MAPK8IP3 RPUSD1 UBE2I MSLN ERVK13-1 TPSB2 ZNF598 LOC107984876 RPL23AP5 CASKIN1 NPW RNF151 MPG EME2 SNORA78 AMDHD2 IGFALS PRSS27 DDX11L10 LOC729652 PDPK1 RHBDL1 MLST8 SSTR5 NARFL LOC105371049 PKD1 CCDC154 LOC652276 MIR1225 LOC107987233 SNRNP25 KCTD5 RAB40C MIR6511B1 TBC1D24 WDR90 LOC105371184 HAGH TSR3 MIR3180-5 SOX8 FAM234A LOC101929280 RGS11 BAIAP3 RAB11FIP3 SYNGR3 LOC105371046 NTHL1 HAGHL SSTR5-AS1 JMJD8 METRN PTX4 TRAF7 FBXL16 LOC106660606 HBQ1 MIR4717 LMF1-AS1 MIR3677 IFT140 CLCN7 UNKL ATP6V0C LMF1 TMEM8A SNORA64 PRR35 WDR24 LUC7L HBA1 SNHG9 PGP GNG13 MIR6767 ABCA3 GNPTG MIR6859-4 E4F1 CACNA1H SNORD60 NOXO1 SNORA10 NUBP2 CAPN15 METTL26 HS3ST6 RAB26 HN1L DECR2 MRPL28 HBM STUB1 SPSB3 MIR662 LINC00254 LOC105371038 HBZ NTN3 MIR3178 PRR25 MIR3176 NDUFB10 NPRL3 TPSAB1 MIR5587 C16orf91 ABCA17P MEIOB TPSG1 WFIKKN1 MIR940 MIR6768 RHBDF1 CCDC78 FAM173A C1QTNF8 LOC105371047 RHOT2 MRPS34 AXIN1 TBL3 LOC100287175 PRSS29P C16orf59 MCRIP2 TSC2 TMEM204 RPL3L FAHD1 NHLRC4 WASIR2 PIGQ TPSD1 POLR3K SLC9A3R2 HBA2 LOC105371045 RNPS1 CRAMP1 PDIA2 NME4 LOC100134368 ECI1
nsv1044142 Chr.16:10765 - 255644 on Build GRCh38 Gain MIR6859-4 HBZ MPG NPRL3 DDX11L10 WASIR2 LUC7L HBQ1 FAM234A POLR3K HBA1 HBA2 RHBDF1 HBM SNRNP25
esv3570031 Chr.16:243389 - 278107 on Build GRCh38 Gain RGS11 FAM234A
esv2667528 Chr.16:246450 - 249976 on Build GRCh38 Deletion FAM234A
esv3637560 Chr.16:246387 - 250231 on Build GRCh38 Loss FAM234A
dgv32n68 Chr.16:245507 - 476226 on Build GRCh38 Loss DECR2 RPL23AP5 MRPL28 RGS11 TMEM8A ARHGDIG RAB11FIP3 PDIA2 NME4 LOC100134368 AXIN1 FAM234A

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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