Genomic Map
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Target Gene Details
Entrez Gene ID: | 581 |
Gene Name: | BCL2 associated X, apoptosis regulator |
Gene Aliases: |
BCL2L4 |
Location: |
Chr.19:48954825-48961798 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BAX | NM_001291428.1 | 6 | 594 | NP_001278357.1 |
| NM_001291431.1 | NP_001278360.1 | |||
| NM_138761.3 | NP_620116.1 | |||
| NM_138763.3 | NP_620118.1 | |||
| NM_138764.4 | NP_620119.2 | |||
| NR_027882.1 | ||||
| XM_017027077.1 | XP_016882566.1 | |||
| AF007826.1 | AAD22706.1 | |||
| AF247393.1 | AAF71267.1 | |||
| AF250190.1 | AAF82094.1 | |||
| AI565203.1 | ||||
| AJ417988.1 | CAD10744.1 | |||
| AK291076.1 | ||||
| BC014175.2 | AAH14175.1 | |||
| BM673184.1 | 1 | 175 | ||
| CN281003.1 | ||||
| JX524562.1 | ||||
| KF830846.1 | ||||
| KF830847.1 | 5 | 474 | ||
| KF830848.1 | 5 | 474 | ||
| L22473.1 | AAA03619.1 | |||
| U19599.1 | AAC50142.1 |
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-C3
EMP3
NUP62
SNAR-A12
NUCB1
PNKP
SLC6A16
CGB5
MIR4751
SPHK2
CARD8-AS1
SNRNP70
SNAR-A11
SNAR-A13
SNORD35B
LOC105372430
DBP
SNORD34
PTH2
AP2A1
TSKS
SNORD33
MIR4749
RPL13A
SNAR-A7
RCN3
SNAR-A4
NOSIP
BCAT2
CGB3
PLEKHA4
FUT1
VRK3
SNAR-B1
HRC
BCL2L12
FTL
FLJ26850
PIH1D1
SNAR-A8
CYTH2
DHDH
ZNF114
TRPM4
IL4I1
PRR12
RRAS
CCDC155
SPACA4
TULP2
SNAR-C2
SNAR-C4
MIR4750
SULT2B1
SNAR-A14
SNORD35A
SNAR-A6
HSD17B14
MIR6800
PRRG2
SIGLEC16
ADM5
PLA2G4C
RPS11
BSPH1
LOC101928295
SNAR-G1
CGB1
CGB7
GRIN2D
TBC1D17
LOC105447645
CA11
SNAR-C1
SNAR-B2
IZUMO1
LHB
NTF4
CARD8
KDELR1
MIR6798
SNAR-G2
FCGRT
SNAR-D
BAX
ZNF473
FUT2
GRWD1
CCDC114
SNAR-C5
MIR150
CGB2
LOC101059948
IRF3
PTOV1
TMEM143
SNAR-A5
MAMSTR
KCNJ14
RUVBL2
PPP1R15A
LIG1
SNAR-A9
ALDH16A1
DKKL1
ATF5
SYNGR4
SCAF1
ELSPBP1
MIR5088
MIR6799
NUCB1-AS1
LMTK3
CGB8
FLT3LG
CD37
RASIP1
SLC17A7
SNAR-A3
LIN7B
NTN5
PTOV1-AS1
SNAR-A1
CABP5
TEAD2
RPL18
C19orf73
PTOV1-AS2
GFY
KCNA7
GYS1
PRMT1
SNORD32A
SIGLEC11
SNAR-A10
AKT1S1
FAM83E
FUZ
PLA2G4C-AS1
SEC1P
CPT1C
SNAR-A2
LOC100287477
MIR4324
PPFIA3
C19orf68
MED25
FGF21
|
| dgv3618n100 | Chr.19:48948950 - 49021211 on Build GRCh38 | Gain |
MIR6798
BAX
RUVBL2
LHB
FTL
LOC101059948
GYS1
|
| nsv833857 | Chr.19:48914476 - 49146320 on Build GRCh38 | Loss |
CGB1
CGB7
CGB8
RUVBL2
DHDH
LHB
NTF4
LIN7B
NUCB1
CGB3
MIR6798
SNAR-G2
C19orf73
BAX
KCNA7
NUCB1-AS1
PPFIA3
CGB5
FTL
CGB2
LOC101059948
GYS1
SNRNP70
SNAR-G1
|
| nsv833856 | Chr.19:48847866 - 48986483 on Build GRCh38 | Loss |
NUCB1
PLEKHA4
BAX
DHDH
TULP2
PPP1R15A
NUCB1-AS1
FTL
GYS1
|
| nsv953598 | Chr.19:48957644 - 49085143 on Build GRCh38 | Deletion |
CGB1
CGB7
CGB8
RUVBL2
LHB
NTF4
CGB3
MIR6798
SNAR-G2
BAX
KCNA7
CGB5
FTL
CGB2
LOC101059948
GYS1
SNRNP70
SNAR-G1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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