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

Chr.16:259943 on build GRCh38
Cytoband
16p13.3
Assay ID Hs02815415_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 Intron 8 - Exon 9
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
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 NTHL1 UBE2I LOC101929280 HBM ATP6V0C PIGQ CCDC154 TBL3 FBXL16 MIR662 MRPL28 NHLRC4 TSR3 AMDHD2 MIR1225 UNKL KCTD5 MSLN MIR4516 SNORA78 CCNF LOC100134368 CEMP1 FAM234A TMEM204 LOC107987233 PDIA2 RHBDL1 NME4 MIR3177 ECI1 PRSS27 MIR3178 IGFALS LOC729652 MEIOB NTN3 TPSAB1 RHBDF1 C1QTNF8 TELO2 LINC00235 NUBP2 STUB1 BAIAP3 CACNA1H NDUFB10 MIR6511B1 NARFL E4F1 HAGHL C16orf91 RAB11FIP3 HBA2 RPUSD1 RPL3L MIR3677 HBQ1 GFER PDPK1 NPRL3 FLJ42627 BRICD5 CCDC78 MIR3176 GNG13 RPS2 CLCN7 RHOT2 LUC7L MIR5587 HBZ RPL23AP5 SNRNP25 CASKIN1 LMF1 MIR940 ZNF598 LMF1-AS1 TMEM8A CRAMP1 METRN SYNGR3 LOC105371045 LINC00254 POLR3K LOC105371046 ERVK13-1 SNHG19 MRPS34 LOC652276 SOX8 AXIN1 MSRB1 LOC107984876 MIR6768 WFIKKN1 SNHG9 HBA1 LOC105371049 MIR6859-4 CAPN15 DNASE1L2 PKD1 MIR4717 FAM173A TPSG1 RAB26 LOC105371038 METTL26 MAPK8IP3 MIR3180-5 TRAF7 SPSB3 GNPTG ARHGDIG TPSD1 TSC2 RGS11 NOXO1 SNORA10 SNORA64 WDR90 HS3ST6 RNF151 WDR24 LOC105371047 MLST8 LOC106660606 PGP ABCA3 WASIR2 NME3 HAGH PRR25 MCRIP2 RAB40C DECR2 RNPS1 SNORD60 EME2 IFT140 HN1L MPG ABCA17P SSTR5 TPSB2 C16orf59 MIR6767 SSTR5-AS1 PRSS29P SLC9A3R2 PRR35 DDX11L10 PTX4 LOC105371184 FAHD1 TBC1D24 JMJD8 LOC100287175 CHTF18 NPW
esv3570031 Chr.16:243389 - 278107 on Build GRCh38 Gain RGS11 FAM234A
dgv32n68 Chr.16:245507 - 476226 on Build GRCh38 Loss DECR2 RGS11 LOC100134368 FAM234A MRPL28 TMEM8A AXIN1 RPL23AP5 ARHGDIG RAB11FIP3 PDIA2 NME4

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More Information


Additional Information:

For this assay, SNP(s) [rs74003710,rs78641696] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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