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 |
 SULT2B1
PPP1R15A
SNORD35B
SNAR-G1
HSD17B14
LHB
CA11
CCDC114
FLT3LG
SNAR-A11
SIGLEC11
SNAR-A9
VRK3
MAMSTR
PTOV1-AS2
NOSIP
BCAT2
SNAR-A1
SNAR-A7
LOC101059948
CCDC155
ZNF473
GYS1
SYNGR4
FAM83E
PPFIA3
SNRNP70
RPL18
SNAR-A6
LMTK3
MIR5088
SPHK2
PLA2G4C-AS1
SNAR-C5
NUP62
DBP
SNAR-A3
KCNJ14
PTOV1-AS1
SNAR-A4
GRWD1
MIR6800
TSKS
RCN3
SNAR-A10
ATF5
SLC17A7
KDELR1
IZUMO1
PIH1D1
LOC100287477
CARD8
PRMT1
DKKL1
CPT1C
SNORD32A
PRRG2
C19orf73
CYTH2
SNAR-A13
TEAD2
SNORD35A
RRAS
BAX
BCL2L12
TULP2
SNAR-C1
FGF21
LIG1
IL4I1
SNAR-C2
AKT1S1
SNAR-A14
LIN7B
PNKP
SNORD33
SNAR-A5
SNORD34
DHDH
ELSPBP1
SNAR-A8
FUT2
PTOV1
PTH2
LOC101928295
ALDH16A1
CGB5
PRR12
NTF4
MIR4324
SIGLEC16
SCAF1
SEC1P
RASIP1
MIR4749
ZNF114
CARD8-AS1
LOC105447645
SNAR-C4
PLA2G4C
NUCB1-AS1
BSPH1
C19orf68
TBC1D17
AP2A1
TRPM4
CGB8
MED25
FCGRT
CGB2
SPACA4
PLEKHA4
RPL13A
ADM5
SNAR-C3
SNAR-D
EMP3
NUCB1
FLJ26850
GFY
SLC6A16
TMEM143
SNAR-B2
FUT1
FTL
MIR6799
IRF3
MIR6798
RPS11
CGB3
CGB1
NTN5
GRIN2D
SNAR-B1
SNAR-G2
SNAR-A12
CABP5
LOC105372430
KCNA7
SNAR-A2
MIR4751
CGB7
MIR4750
RUVBL2
FUZ
MIR150
HRC
CD37
|
| dgv3618n100 | Chr.19:48948950 - 49021211 on Build GRCh38 | Gain |
MIR6798
LHB
BAX
RUVBL2
LOC101059948
GYS1
FTL
|
| nsv833857 | Chr.19:48914476 - 49146320 on Build GRCh38 | Loss |
SNAR-G1
LHB
SNAR-G2
PPFIA3
NUCB1-AS1
SNRNP70
KCNA7
DHDH
CGB8
CGB7
BAX
RUVBL2
FTL
CGB2
MIR6798
CGB5
NTF4
CGB3
CGB1
LIN7B
NUCB1
LOC101059948
GYS1
C19orf73
|
| nsv953598 | Chr.19:48957644 - 49085143 on Build GRCh38 | Deletion |
SNAR-G1
LHB
SNAR-G2
SNRNP70
KCNA7
CGB8
CGB7
BAX
RUVBL2
FTL
CGB2
MIR6798
CGB5
NTF4
CGB3
CGB1
LOC101059948
GYS1
|
| nsv833856 | Chr.19:48847866 - 48986483 on Build GRCh38 | Loss |
TULP2
PPP1R15A
PLEKHA4
NUCB1-AS1
DHDH
BAX
NUCB1
GYS1
FTL
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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