Genomic Map
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Target Gene Details
Entrez Gene ID: | 57333 |
Gene Name: | reticulocalbin 3 |
Gene Aliases: |
RLP49 |
Location: |
Chr.19:49527579-49543638 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RCN3 | NM_020650.2 | 7 | 1818 | NP_065701.2 |
| XM_005259089.3 | 8 | 1913 | XP_005259146.1 | |
| XM_011527143.1 | 8 | 2007 | XP_011525445.1 | |
| XM_017027023.1 | 7 | 2092 | XP_016882512.1 | |
| AF183423.1 | 6 | 1403 | AAG09692.1 | |
| AY195859.1 | 7 | 1818 | AAO43054.1 | |
| AY358423.1 | 7 | 1405 | AAQ88789.1 | |
| BC013436.1 | 7 | 1401 | AAH13436.1 |
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-A12
FAM83E
SPHK2
DHDH
CD37
LMTK3
MIR6798
TULP2
FGF21
PPFIA3
MIR6799
MIR4750
SNAR-C5
SNAR-C4
SNAR-C3
SNAR-A5
ZNF473
BSPH1
TMEM143
SNAR-A10
BCAT2
DKKL1
FUT2
MIR150
IZUMO1
SNRNP70
PTOV1
LOC100287477
IRF3
LOC101928295
SPACA4
CGB1
KCNJ14
SNAR-A6
GRIN2D
C19orf73
SEC1P
BAX
NUP62
MIR4749
SNORD32A
NUCB1
GYS1
SNAR-D
CGB2
LIG1
SYNGR4
CGB7
LIN7B
SCAF1
CARD8-AS1
MIR6800
SNAR-A11
PPP1R15A
ALDH16A1
AKT1S1
MED25
MIR4324
LOC105372430
MIR5088
TEAD2
SNAR-A13
PRRG2
KCNA7
LOC105447645
PLEKHA4
PNKP
KDELR1
SNAR-A7
SIGLEC16
DBP
PLA2G4C-AS1
GRWD1
SNAR-G1
CCDC155
RPL18
FLJ26850
TBC1D17
CGB8
ZNF114
PRMT1
RASIP1
SNAR-B1
RCN3
SNAR-A14
PTOV1-AS2
ATF5
SNAR-G2
SLC6A16
SNAR-A1
SNORD35B
PRR12
PTOV1-AS1
ELSPBP1
CPT1C
PIH1D1
SNAR-C2
FUZ
SNORD33
CA11
SNAR-C1
IL4I1
TRPM4
FUT1
RPL13A
SNORD34
MIR4751
SLC17A7
HRC
LOC101059948
NUCB1-AS1
BCL2L12
CGB5
SNAR-A2
TSKS
CABP5
SIGLEC11
HSD17B14
NOSIP
FLT3LG
CGB3
SNAR-A4
SNAR-A3
FTL
VRK3
LHB
GFY
EMP3
SNAR-A9
CYTH2
CARD8
MAMSTR
RRAS
PLA2G4C
AP2A1
SNAR-B2
C19orf68
ADM5
FCGRT
SULT2B1
SNAR-A8
RUVBL2
CCDC114
SNORD35A
PTH2
NTN5
RPS11
NTF4
|
| nsv833863 | Chr.19:49479177 - 49629716 on Build GRCh38 | Loss |
RCN3
RPL13A
PRRG2
SNORD34
NOSIP
FCGRT
FLT3LG
SNORD33
SNORD35B
PRR12
SNORD35A
SNORD32A
RPS11
MIR150
|
| nsv833862 | Chr.19:49448789 - 49570676 on Build GRCh38 | Loss |
RCN3
RPL13A
SNORD34
NOSIP
FCGRT
PIH1D1
FLT3LG
SNORD33
SNORD35B
ALDH16A1
SNORD35A
SNORD32A
RPS11
MIR150
|
| nsv1160655 | Chr.19:49489110 - 49841830 on Build GRCh38 | Deletion |
RCN3
RPL13A
SNORD34
BCL2L12
TSKS
SCAF1
NOSIP
MIR6799
MIR6800
SNORD35B
PRR12
PTOV1-AS1
MED25
MIR5088
MIR150
RRAS
PRRG2
IRF3
AP2A1
CPT1C
ADM5
FCGRT
FUZ
SNORD33
SNORD35A
SNORD32A
RPS11
PRMT1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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