Assay Details
Target Gene Details
Entrez Gene ID: | 2217 |
Gene Name: | Fc fragment of IgG receptor and transporter |
Gene Aliases: |
FCRN, alpha-chain |
Location: |
Chr.19:49512279-49526428 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FCGRT | NM_001136019.2 | NP_001129491.1 | ||
NM_004107.4 | NP_004098.1 | |||
XM_005258657.1 | XP_005258714.1 | |||
XM_011526627.2 | XP_011524929.1 | |||
AK074734.1 | 1 | 707 | ||
AK075510.1 | ||||
AK075532.1 | ||||
AK299124.1 | ||||
BC008734.2 | AAH08734.1 | |||
BI520292.1 | ||||
BT006828.1 | AAP35474.1 | |||
BX647163.1 | CAI46032.1 | |||
DC312637.1 | ||||
U12255.1 | AAA58958.1 |
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 | DBP SNORD35B C19orf73 SNRNP70 BCL2L12 SNORD33 IRF3 FUT1 NUCB1-AS1 PTOV1-AS2 SNAR-A4 PNKP ADM5 SNAR-D PPFIA3 NUP62 GRIN2D LMTK3 SNAR-A13 HRC MIR6799 PLA2G4C-AS1 PTH2 RPL13A LOC101059948 LIN7B FGF21 TMEM143 RPS11 FLT3LG SIGLEC16 CCDC114 MIR5088 MIR4751 RPL18 CA11 BSPH1 ELSPBP1 MAMSTR LHB KCNJ14 CCDC155 PTOV1-AS1 CGB8 MIR4749 SNAR-B1 MIR6798 SNAR-G1 TRPM4 MIR150 FLJ26850 SNAR-A11 CPT1C NOSIP SPACA4 FUT2 PIH1D1 SNAR-A5 RRAS MIR6800 FTL RCN3 SCAF1 KCNA7 SNAR-B2 PRR12 CARD8-AS1 DHDH ZNF473 SNORD35A NTN5 LIG1 MIR4324 AP2A1 SULT2B1 SNAR-A6 SLC17A7 DKKL1 SNAR-C2 ZNF114 PRRG2 CABP5 CD37 LOC100287477 SYNGR4 CGB3 CGB5 AKT1S1 KDELR1 MED25 SNAR-C3 IL4I1 GYS1 SNAR-A14 SNAR-A9 NTF4 SIGLEC11 SLC6A16 SNAR-A7 HSD17B14 PTOV1 EMP3 RUVBL2 PRMT1 BCAT2 LOC105447645 SNORD34 FUZ SNAR-C1 PLA2G4C SNAR-C4 C19orf68 GRWD1 VRK3 SEC1P ATF5 CYTH2 TSKS FCGRT GFY PPP1R15A SNAR-C5 NUCB1 IZUMO1 CARD8 SNAR-A2 TEAD2 SNAR-A1 ALDH16A1 SNAR-A10 CGB7 SNAR-A8 SNAR-A12 PLEKHA4 FAM83E MIR4750 RASIP1 LOC101928295 SPHK2 SNAR-G2 LOC105372430 BAX SNAR-A3 CGB2 CGB1 SNORD32A TULP2 TBC1D17 |
nsv833863 | Chr.19:49479177 - 49629716 on Build GRCh38 | Loss | RCN3 FCGRT SNORD35B PRRG2 PRR12 MIR150 RPL13A SNORD33 NOSIP SNORD35A SNORD32A RPS11 SNORD34 FLT3LG |
nsv833862 | Chr.19:49448789 - 49570676 on Build GRCh38 | Loss | RCN3 FCGRT SNORD35B MIR150 RPL13A SNORD33 NOSIP SNORD35A SNORD32A ALDH16A1 RPS11 PIH1D1 SNORD34 FLT3LG |
nsv1160655 | Chr.19:49489110 - 49841830 on Build GRCh38 | Deletion | TSKS FCGRT SNORD35B PRRG2 PTOV1-AS1 BCL2L12 MIR150 SNORD33 IRF3 CPT1C NOSIP ADM5 RRAS MIR6800 MED25 RCN3 SCAF1 MIR6799 PRR12 RPL13A SNORD35A SNORD32A PRMT1 RPS11 SNORD34 AP2A1 FUZ MIR5088 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |