Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 10856 |
Gene Name: | RuvB like AAA ATPase 2 |
Gene Aliases: |
CGI-46, ECP-51, ECP51, INO80J, REPTIN, RVB2, TAP54-beta, TIH2, TIP48, TIP49B |
Location: |
Chr.19:48993448-49015995 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 7 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RUVBL2 | NM_001321190.1 | NP_001308119.1 | ||
| NM_001321191.1 | NP_001308120.1 | |||
| NM_006666.2 | NP_006657.1 | |||
| NR_135578.1 | ||||
| XM_011526330.1 | XP_011524632.1 | |||
| AB024301.1 | BAA76708.1 | |||
| AF124607.1 | AAF87087.1 | |||
| AF151804.1 | AAD34041.1 | |||
| AF155138.1 | AAD38073.1 | |||
| AK027762.1 | ||||
| AK057498.1 | ||||
| AK074542.1 | BAC11048.1 | |||
| AK301344.1 | ||||
| AL136743.1 | CAB66677.1 | |||
| BC000428.2 | AAH00428.1 | |||
| BC004531.2 | AAH04531.1 | |||
| BC008355.1 | AAH08355.1 | |||
| CR533507.1 | CAG38538.1 | |||
| Y18417.1 | CAB46270.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833859 | Chr.19:48997009 - 49173266 on Build GRCh38 | Loss |
 NTF4
CGB2
KCNA7
MIR6798
CGB1
LHB
CGB8
SNRNP70
HRC
SNAR-G2
C19orf73
TRPM4
CGB3
SNAR-G1
CGB7
LIN7B
LOC101059948
RUVBL2
PPFIA3
CGB5
|
| nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss |
BSPH1
DKKL1
CD37
DHDH
PPP1R15A
GRIN2D
SNAR-B1
ALDH16A1
C19orf68
SPHK2
SNAR-G1
EMP3
SNAR-A2
SNORD33
PPFIA3
PLA2G4C-AS1
PTOV1-AS1
SNAR-C5
MIR6800
SNORD32A
LOC101928295
SNAR-A9
ZNF473
CABP5
MIR6799
DBP
NUP62
MIR5088
BCAT2
SNAR-C3
TULP2
AKT1S1
MIR4751
PTH2
PRR12
SNAR-C2
CGB1
RASIP1
TSKS
CARD8
BAX
SIGLEC11
SNAR-A10
CGB7
CA11
PIH1D1
PTOV1-AS2
MIR4324
SNAR-A14
SNAR-A13
IL4I1
SNAR-B2
GYS1
MAMSTR
HRC
CYTH2
NUCB1
SNAR-A6
SNAR-G2
SNAR-A4
RPL13A
SNAR-A11
FGF21
FLT3LG
SNAR-A8
SNAR-A12
PLEKHA4
RPL18
LOC105372430
SNAR-C1
KDELR1
CARD8-AS1
SNAR-C4
NTF4
GFY
MED25
LHB
CCDC155
TEAD2
SNRNP70
CPT1C
SYNGR4
IRF3
MIR4749
CCDC114
SULT2B1
TMEM143
AP2A1
ATF5
PLA2G4C
CGB5
SNAR-A3
SNORD35B
CGB2
FCGRT
SPACA4
LMTK3
HSD17B14
FTL
KCNJ14
LOC100287477
C19orf73
MIR150
SIGLEC16
SLC6A16
LIN7B
SNAR-A1
RCN3
SNAR-A7
RUVBL2
ADM5
PTOV1
KCNA7
MIR6798
FUT2
SLC17A7
VRK3
FUZ
NOSIP
PRMT1
BCL2L12
RRAS
FAM83E
SNORD34
MIR4750
ELSPBP1
IZUMO1
FUT1
CGB8
PRRG2
FLJ26850
TBC1D17
ZNF114
SNORD35A
PNKP
SNAR-D
TRPM4
CGB3
LIG1
GRWD1
LOC101059948
NUCB1-AS1
RPS11
SCAF1
LOC105447645
SNAR-A5
SEC1P
NTN5
|
| dgv3618n100 | Chr.19:48948950 - 49021211 on Build GRCh38 | Gain |
LOC101059948
MIR6798
RUVBL2
LHB
GYS1
FTL
BAX
|
| nsv833857 | Chr.19:48914476 - 49146320 on Build GRCh38 | Loss |
NTF4
CGB2
KCNA7
MIR6798
CGB1
LHB
CGB8
SNRNP70
DHDH
GYS1
FTL
NUCB1
BAX
SNAR-G2
C19orf73
CGB3
SNAR-G1
CGB7
LIN7B
LOC101059948
NUCB1-AS1
RUVBL2
PPFIA3
CGB5
|
| nsv953598 | Chr.19:48957644 - 49085143 on Build GRCh38 | Deletion |
NTF4
CGB2
KCNA7
MIR6798
CGB1
LHB
CGB8
SNRNP70
GYS1
FTL
BAX
SNAR-G2
CGB3
SNAR-G1
CGB7
LOC101059948
RUVBL2
CGB5
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs115058775] 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
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top