BCL11B: BAF chromatin remodeling complex subunit BCL11B
Lollipop plot
Phosphosites location and occurrence
Select Y-axis:
Sample number
Cohort number
* Hover over the dots to see sequence motif and cohorts.
Phosphosite detection coverage
The frequency of phosphosite detection in the number of cohorts and tumor and normal samples
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BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
Site
Sequence
Cohorts
Total
T
N
T
N
T
N
T
N
T
N
T
N
T
N
T
N
T
N
T
N
S13 QGNPQHLS QRELITP 1 20 - - - - - - - - - - 10 10 - - - - - - - - S97 DKALDKDS PPPSSRS 8 872 - - 54 47 84 86 - - 108 62 79 74 41 36 35 8 105 44 7 2 T120 VEIGIQVT PDEDDHL 4 81 - - 25 16 - - - - - - 5 4 12 12 - - 5 2 - - S129 DEDDHLLS PTKGICP 7 207 - - 4 4 27 18 27 - 36 19 9 9 - - - - 35 13 6 - S256 YLEPGPAS SSLTPRL 1 8 - - - - - - - - - - - - 4 4 - - - - - - S257 LEPGPASS SLTPRLT 1 8 - - 4 4 - - - - - - - - - - - - - - - - S258 EPGPASSS LTPRLTI 1 16 - - 8 8 - - - - - - - - - - - - - - - - T260 GPASSSLT PRLTIPP 9 758 - - 8 8 62 55 18 - 91 52 83 77 59 52 50 11 69 30 17 16 S277 GPEAVAQS PLMNFLG 7 321 - - 32 30 17 10 27 - 104 58 5 4 12 13 - - 7 2 - - T313 GEGRLPGT PPLFSPP 5 92 - - - - - - - - 5 3 15 13 - - 36 6 3 2 7 2
Tumor and normal comparison
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Site
Sequence
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
S13 QGNPQHLS QRELITP - - - - - - - - - - - S97 DKALDKDS PPPSSRS 3.6e-49 - 1.8e-7 5.6e-12 - 7.9e-16 2.1e-21 0.4 - 2.1e-8 - T120 VEIGIQVT PDEDDHL 1.5e-3 - 1.5e-3 - - - - - - - - S129 DEDDHLLS PTKGICP 0.001 - - 1.5e-4 - 0.29 - - - 0.4 - S256 YLEPGPAS SSLTPRL - - - - - - - - - - - S257 LEPGPASS SLTPRLT - - - - - - - - - - - S258 EPGPASSS LTPRLTI - - - - - - - - - - - T260 GPASSSLT PRLTIPP 8.1e-16 - - 0.31 - 1.5e-11 2e-14 3.7e-3 -0.13 3.3e-3 - S277 GPEAVAQS PLMNFLG -6.2e-4 - 0.93 - - -8.2e-7 - - - - - T313 GEGRLPGT PPLFSPP - - - - - - - - - - -
* P-values are from Wilcoxon rank sum test and can be clicked to show the box plots. Positive values mean higher abundance in tumor. BRCA and GBM do not have normal samples.
Phenotype and mutation association
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all sites
S13
S97
T120
S129
S256
S257
S258
T260
S277
T313
S318
S358
S375
T376
S381
S398
S401
T406
T417
S465
S483
S488
S493
S496
S497
S503
S678
S683
S740
S741
S744
S745
T754
S768
S772
S775
T776
S788
S789
all
clinical
pathway
cell type
genomic
mutation
Signed p-values
Phenotype
Site
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found
* P-values could be from test for Spearman correlation, Wilcoxon rank sum test, Jonckheere-Terpstra trend test or Cox regression depending on the data type. P-values for individual cohorts can be clicked to show the data plots.
Cis-association
BRCA S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation CCRCC S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation COAD S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation GBM S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation HNSCC S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation LSCC S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation LUAD S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation OV S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation PDAC S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation UCEC S13 S97 T120 S129 S256 S257 S258 T260 S277 T313 S318 S358 S375 T376 S381 S398 S401 T406 T417 S465 S483 S488 S493 S496 S497 S503 S678 S683 S740 S741 S744 S745 T754 S768 S772 S775 T776 S788 S789 protein RNA SCNV methylation
* The circles can be clicked to show the scatter plots. The color and size of the circles correlate with the Spearman correlation coefficients.
Kinase association
Protein
RNA
SCNV
methylation
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all sites
S13
S97
T120
S129
S256
S257
S258
T260
S277
T313
S318
S358
S375
T376
S381
S398
S401
T406
T417
S465
S483
S488
S493
S496
S497
S503
S678
S683
S740
S741
S744
S745
T754
S768
S772
S775
T776
S788
S789
Signed p-values
Kinase
Site
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found
* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots.
Phosphatase association
Protein
RNA
SCNV
methylation
Loading, please wait
all sites
S13
S97
T120
S129
S256
S257
S258
T260
S277
T313
S318
S358
S375
T376
S381
S398
S401
T406
T417
S465
S483
S488
S493
S496
S497
S503
S678
S683
S740
S741
S744
S745
T754
S768
S772
S775
T776
S788
S789
Signed p-values
Phosphatase
Site
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found
* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots.