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 IL4I1 CNV Assays ›
Gene Symbol
IL4I1
Assay Reference Genome
Location

Chr.19:49907372 on build GRCh38
Cytoband
19q13.33
Assay ID Hs02126982_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 259307

Gene Name:

 interleukin 4 induced 1

Gene Aliases:

 FIG1, LAAO, LAO

Location:

 Chr.19:49889654-49929539 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
IL4I1 NM_001258017.1 NP_001244946.1
NM_001258018.1 NP_001244947.1
NM_172374.2 NP_758962.1
NR_047577.1
AJ880386.1 CAI54291.1
AJ880387.1 CAI54292.1
AJ880388.1 CAI54293.1
AJ880389.1
BC131625.1
DQ079587.1 AAZ32711.1
DQ079588.1 AAZ32712.1
DQ079589.1 AAZ32713.1

Target Gene Details

Entrez Gene ID:

 23636

Gene Name:

 nucleoporin 62

Gene Aliases:

 IBSN, SNDI, p62

Location:

 Chr.19:49906825-49929731 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NUP62 NM_001193357.1 2 2639 NP_001180286.1
NM_012346.4 2 2680 NP_036478.2
NM_016553.4 3 3041 NP_057637.2
NM_153718.3 2 2719 NP_714940.1
NM_153719.3 3 2874 NP_714941.1
AF318357.1 3 1419 AAL55864.1
AL162061.1 2 2641 CAB82399.1
BM672281.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3644628 Chr.19:49861781 - 49908526 on Build GRCh38 Gain MIR4750 NUP62 AKT1S1 TBC1D17 IL4I1 PNKP
nsv9739 Chr.19:47901840 - 50143063 on Build GRCh38 Gain+Loss PTOV1-AS1 SPACA4 MIR4324 SCAF1 FCGRT SNAR-C2 RRAS BCAT2 MIR4751 SNAR-C3 CGB5 SLC6A16 NTF4 AKT1S1 SNAR-A2 SNAR-A7 LOC101928295 NTN5 CGB1 CABP5 IL4I1 MIR6799 RPS11 SNAR-A1 ZNF473 LMTK3 BSPH1 HSD17B14 CPT1C SNAR-A8 C19orf73 LIG1 SNAR-D PTOV1 FGF21 GYS1 LOC101059948 NOSIP SNORD33 LOC100287477 KCNA7 CARD8-AS1 RUVBL2 SPHK2 CGB3 KDELR1 PLEKHA4 PRMT1 TMEM143 C19orf68 AP2A1 MED25 FLJ26850 PRRG2 LHB SNAR-C1 ADM5 LOC105372430 CARD8 PTOV1-AS2 MAMSTR RASIP1 PPFIA3 PRR12 SNAR-A10 BCL2L12 VRK3 CGB8 IRF3 SIGLEC11 EMP3 NUCB1 DBP LOC105447645 PTH2 RPL13A MIR4749 MIR4750 FUT1 CGB7 DHDH GFY PIH1D1 SIGLEC16 SNAR-B1 SNAR-A11 GRWD1 FUZ DKKL1 CA11 SNAR-A3 PPP1R15A MIR6800 HRC PLA2G4C SNORD35B FTL SYNGR4 MIR6798 TEAD2 PLA2G4C-AS1 RCN3 SNAR-A4 IZUMO1 TRPM4 SNAR-C5 FLT3LG CCDC155 SULT2B1 CYTH2 SLC17A7 SNAR-G2 SNAR-G1 LIN7B KCNJ14 SNAR-A9 SEC1P CGB2 TBC1D17 MIR150 SNRNP70 SNORD32A NUP62 BAX MIR5088 ZNF114 RPL18 SNORD34 SNAR-A5 SNAR-A6 SNAR-A14 FAM83E SNAR-B2 ELSPBP1 SNAR-A12 SNAR-A13 ATF5 SNAR-C4 CCDC114 TSKS GRIN2D PNKP ALDH16A1 SNORD35A CD37 TULP2 NUCB1-AS1 FUT2
dgv53n68 Chr.19:49724393 - 49943224 on Build GRCh38 Loss PTOV1-AS1 MIR6800 TBC1D17 PTOV1-AS2 ATF5 MIR4751 TSKS MIR4749 PNKP MIR4750 NUP62 PTOV1 AP2A1 AKT1S1 MED25 FUZ IL4I1 MIR6799
nsv953600 Chr.19:49555044 - 49938043 on Build GRCh38 Deletion PTOV1-AS1 TBC1D17 SCAF1 RRAS MIR4751 MIR4749 PRMT1 MIR4750 NUP62 AP2A1 MIR5088 AKT1S1 MED25 PRRG2 ADM5 FUZ IL4I1 MIR6799 MIR6800 PTOV1-AS2 CPT1C ATF5 TSKS PNKP PRR12 BCL2L12 PTOV1 NOSIP IRF3
esv3644630 Chr.19:49877826 - 50039767 on Build GRCh38 Gain MIR4750 SIGLEC11 NUP62 ZNF473 AKT1S1 TBC1D17 VRK3 SIGLEC16 ATF5 MIR4751 IL4I1
esv3583457 Chr.19:49899154 - 49912462 on Build GRCh38 Loss NUP62 IL4I1
dgv54n68 Chr.19:49848512 - 50008788 on Build GRCh38 Loss SIGLEC11 PTOV1-AS1 TBC1D17 PTOV1-AS2 ATF5 MIR4751 MIR4749 PNKP MIR4750 NUP62 PTOV1 AKT1S1 VRK3 SIGLEC16 IL4I1
esv996372 Chr.19:49902955 - 49908214 on Build GRCh38 Deletion NUP62 IL4I1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs151270836,rs75368221] 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

Panther Classification:

Molecular Function -

oxidase transporter

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products