accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

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

Chr.16:268362 on build GRCh38
Cytoband
16p13.3
Assay ID Hs00252409_cn
Size
Availability Made To Order
Catalog # 4400291
Price 4,505.00
Your Price
Online offer:
4505.0
Check your price ›

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 17
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM234A NR_104317.1
AK057165.1 BAB71374.1
AK294581.1

Target Gene Details

Entrez Gene ID:

 8786

Gene Name:

 regulator of G-protein signaling 11

Gene Aliases:

 RS11

Location:

 Chr.16:268301-275943 on Build GRCh38

Assay Gene Location:

 Within Exon 20
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RGS11 NM_001286485.1 16 2310 NP_001273414.1
NM_001286486.1 15 2178 NP_001273415.1
NM_003834.2 17 2354 NP_003825.1
NM_183337.2 17 2343 NP_899180.1
XM_011522719.2 18 2437 XP_011521021.1
XM_011522720.2 18 2377 XP_011521022.1
AB209582.1 9 4251 BAD92819.1
AF035153.1 17 2314 AAC69175.1
AF035154.1 17 2325 AAC69176.1
AK091701.1 15 2175
BC141803.1 17 2318
CK299324.1 1 80

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv1479e59 Chr.16:267152 - 268350 on Build GRCh38 Duplication RGS11 FAM234A
esv2422427 Chr.16:10001 - 2723164 on Build GRCh38 Duplication LOC652276 MEIOB FAM173A MLST8 RHBDL1 TRAF7 ZNF598 ECI1 RPUSD1 CHTF18 NME4 TPSB2 CASKIN1 MSLN RHOT2 NARFL NDUFB10 PRR25 GNPTG UNKL LOC105371049 MIR6768 RPS2 NPRL3 DNASE1L2 DECR2 SYNGR3 MIR940 CEMP1 CCDC78 WFIKKN1 SNORD60 LOC105371184 AXIN1 SNORA10 WDR90 BAIAP3 LOC100287175 HAGHL MIR3176 LOC106660606 UBE2I PKD1 HBQ1 LOC105371045 MAPK8IP3 TSC2 MIR4516 MIR3180-5 RGS11 PRSS27 LOC101929280 RNPS1 MIR6859-4 LOC105371047 C1QTNF8 STUB1 PIGQ RPL3L MIR3677 ABCA17P WDR24 MIR5587 BRICD5 LOC107987233 LOC105371038 HBA1 CACNA1H E4F1 NOXO1 SLC9A3R2 HBM PRR35 SNORA64 GNG13 HN1L NUBP2 MCRIP2 SNHG9 C16orf91 SPSB3 METRN RAB26 NME3 NTN3 FAHD1 MIR6511B1 TPSD1 MSRB1 LOC729652 LINC00254 MIR3177 LOC107984876 RNF151 RAB40C EME2 SNORA78 TSR3 FAM234A SSTR5 LMF1 KCTD5 PGP GFER MIR662 MIR4717 CCDC154 WASIR2 CLCN7 FBXL16 JMJD8 SOX8 RPL23AP5 SSTR5-AS1 TMEM204 SNRNP25 IFT140 DDX11L10 MIR1225 TPSAB1 NHLRC4 MPG TPSG1 MIR3178 ABCA3 METTL26 LINC00235 MIR6767 LOC105371046 TELO2 ARHGDIG C16orf59 HS3ST6 NPW TBC1D24 CAPN15 CCNF AMDHD2 POLR3K ATP6V0C LOC100134368 LMF1-AS1 PDPK1 MRPL28 LUC7L CRAMP1 HBZ RAB11FIP3 PTX4 HAGH HBA2 IGFALS RHBDF1 MRPS34 PRSS29P ERVK13-1 TMEM8A FLJ42627 PDIA2 SNHG19 TBL3 NTHL1
esv3570031 Chr.16:243389 - 278107 on Build GRCh38 Gain RGS11 FAM234A
esv3637563 Chr.16:263248 - 505590 on Build GRCh38 Gain AXIN1 ARHGDIG RPL23AP5 RGS11 NME4 RAB11FIP3 LOC100134368 FAM234A TMEM8A DECR2 PDIA2 MRPL28
nsv827477 Chr.16:262247 - 297639 on Build GRCh38 Gain AXIN1 ARHGDIG RGS11 FAM234A PDIA2
esv3637561 Chr.16:261769 - 271795 on Build GRCh38 Loss RGS11 FAM234A
dgv32n68 Chr.16:245507 - 476226 on Build GRCh38 Loss AXIN1 ARHGDIG RPL23AP5 RGS11 NME4 RAB11FIP3 LOC100134368 FAM234A TMEM8A DECR2 PDIA2 MRPL28

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs76735572] 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 Exonic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products