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