Assay Details
Target Gene Details
Entrez Gene ID: | 2323 |
Gene Name: | fms related tyrosine kinase 3 ligand |
Gene Aliases: |
FL, FLT3L |
Location: |
Chr.19:49474172-49487038 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FLT3LG | XM_005258682.4 | 7 | 1169 | XP_005258739.3 |
AK301136.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss | SNAR-A6 CGB8 IZUMO1 FUT2 MIR5088 RPL13A MIR4751 SLC6A16 KCNA7 DBP SNAR-A11 HSD17B14 LOC105372430 SNAR-A14 SNAR-C3 C19orf73 SNAR-A7 CGB1 KCNJ14 BCAT2 TBC1D17 IL4I1 PPP1R15A RRAS LHB FTL RPL18 SIGLEC11 LOC105447645 ADM5 MED25 PRRG2 PTOV1 BAX PTH2 CABP5 PLEKHA4 SNORD33 PTOV1-AS1 HRC TSKS KDELR1 TEAD2 SIGLEC16 LOC100287477 SNAR-A13 PLA2G4C-AS1 MIR4324 MIR150 RCN3 ELSPBP1 EMP3 SNAR-A1 PRMT1 SNAR-A12 IRF3 CA11 ZNF473 CGB2 ALDH16A1 SNAR-A3 RUVBL2 RPS11 LIG1 FLT3LG SNRNP70 MIR6800 CPT1C SNAR-D LIN7B GRIN2D CGB5 TULP2 NUP62 PTOV1-AS2 FLJ26850 SNAR-A10 SCAF1 MIR4750 SNORD32A CGB7 FUZ SPHK2 PNKP MIR4749 SNORD34 SNAR-C4 PIH1D1 SEC1P GYS1 SNAR-A2 C19orf68 MIR6798 RASIP1 CYTH2 NOSIP SPACA4 VRK3 PPFIA3 NUCB1 NUCB1-AS1 SNAR-A8 SLC17A7 SNAR-A4 NTF4 FGF21 LOC101059948 SNAR-C5 NTN5 LOC101928295 FUT1 MIR6799 SNAR-B1 BSPH1 SNAR-A5 AP2A1 SNAR-C2 FAM83E PRR12 ATF5 SNAR-B2 SNAR-A9 CARD8-AS1 ZNF114 PLA2G4C SNORD35A DKKL1 SNORD35B SNAR-C1 SULT2B1 DHDH SYNGR4 TMEM143 BCL2L12 LMTK3 FCGRT CGB3 GFY AKT1S1 MAMSTR SNAR-G1 CCDC155 CD37 GRWD1 TRPM4 CARD8 SNAR-G2 CCDC114 |
nsv833863 | Chr.19:49479177 - 49629716 on Build GRCh38 | Loss | SNORD33 FCGRT PRR12 NOSIP RPS11 MIR150 SNORD32A SNORD35A RPL13A FLT3LG PRRG2 SNORD35B RCN3 SNORD34 |
nsv833862 | Chr.19:49448789 - 49570676 on Build GRCh38 | Loss | SNORD33 FCGRT ALDH16A1 NOSIP RPS11 MIR150 SNORD32A SNORD35A RPL13A FLT3LG SNORD35B RCN3 SNORD34 PIH1D1 |
nsv953599 | Chr.19:49386444 - 49506743 on Build GRCh38 | Deletion | SNORD33 ALDH16A1 RPS11 MIR150 SNORD32A SNORD35A RPL13A FLT3LG GFY SNORD35B SLC17A7 SNORD34 CCDC155 PTH2 PIH1D1 LOC101928295 |
More Information
Additional Information:
For this assay, SNP(s) [rs115587522] 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 DGV Variation |