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Bladder
BL8106
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BL8106
Contact Model Developer
Model Contact
Model: BL8106
Model Contact: Seth Lerner
Institution: BCM Bladder PDX Program
Email:
bladdercan@bcm.edu
Patient Information
Clinical Timeline
Clinical Information at Collection
Pathology Information at Collection
Model Information for Model: BL8106
Model Details - Initial Implantation of Patient Tissue
Mutations (Cancer Gene Census List)
Show/Hide Columns
The number of models in this collection with mutations in the listed gene;
may include models that are not publicly available for distribution.
The number of models in this collection with mutations at the listed site;
may include models that are not publicly available for distribution.
Total mutations showing: 478
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
Download
Gene
Filter by Gene
Chr
Filter by Chr
Start
End
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Alt
cDNA Change
Codon Change
Protein Change
TVAF
Gene Mutation Freq.
Site Mutation Freq.
Most Severe Effect
All Effects
Mutation Impact
Transcript ID
ClinVar Clinical Significance
COSMIC ID
gnomAD Non-Cancer AF
dbSNP ID
Gene Mutation Freq.
Site Mutation Freq.
Transcript ID
ClinVar Clinical Significance
COSMIC ID
dbSNP ID
A1CF
chr10
50809906
50809909
TAGC
T
c.1594_1596del
GCT/-
p.A532del
0.062
2
2
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000373997.8
COSV50964203
rs747104061
2
2
ENST00000373997.8
COSV50964203
rs747104061
ABL1
chr9
130884102
130884105
CAAG
C
c.1826_1828del
AAG/-
p.K609del
0.028
6
6
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000318560.6
COSV59324524
rs201725154
6
6
ENST00000318560.6
COSV59324524
rs201725154
ABL2
chr1
179108917
179108917
T
A
c.2350A>T
Aca/Tca
p.T784S
0.525
1
1
Missense Variant
Missense Variant
MODERATE
ENST00000502732.6
Likely_benign
COSV105243257
0.003241380000
rs55892721
1
1
ENST00000502732.6
Likely_benign
COSV105243257
rs55892721
ACSL6
chr5
131966526
131966526
C
T
c.1603G>A
Gtg/Atg
p.V535M
0.059
1
1
Missense Variant
Missense Variant
MODERATE
ENST00000651883.2
.
1
1
ENST00000651883.2
.
AFDN
chr6
167952115
167952118
CGAG
C
c.4629_4631del
GAG/-
p.E1543del
0.04
7
1
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000366806.6
rs540265332
7
1
ENST00000366806.6
rs540265332
AFDN
chr6
167966011
167966014
TGAG
T
c.5091_5093del
GAG/-
p.E1697del
0.038
7
7
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000366806.6
COSV60040388
.
7
7
ENST00000366806.6
COSV60040388
.
AKAP9
chr7
92085597
92085597
C
T
c.8935C>T
Cct/Tct
p.P2979S
0.968
7
7
Missense Variant
Missense Variant
MODERATE
ENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000
rs1063242
7
7
ENST00000356239.8
Benign/Likely_benign
COSV104663065
rs1063242
ALK
chr2
29193706
29193706
T
C
c.4381A>G
Atc/Gtc
p.I1461V
0.992
8
8
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV101201052
0.997594000000
rs1670283
8
8
ENST00000389048.8
Benign
COSV101201052
rs1670283
ANK1
chr8
41661926
41661926
C
T
c.5494G>A
Gtt/Att
p.V1832I
0.025
4
1
Missense Variant
Missense Variant
MODERATE
ENST00000289734.13
.
4
1
ENST00000289734.13
.
ANK1
chr8
41688189
41688189
C
T
c.4225G>A
Gtt/Att
p.V1409I
0.515
4
1
Missense Variant
Missense Variant
MODERATE
ENST00000289734.13
0.000227892000
rs199760447
4
1
ENST00000289734.13
rs199760447
APC
chr5
112841059
112841059
T
A
c.5465T>A
gTc/gAc
p.V1822D
0.983
7
7
Missense Variant
Missense Variant
MODERATE
ENST00000257430.9
Benign
COSV57321643
0.794920000000
rs459552
7
7
ENST00000257430.9
Benign
COSV57321643
rs459552
APOBEC3B
chr22
38984190
38984190
C
T
c.133C>T
Cgc/Tgc
p.R45C
0.514
1
1
Missense Variant
Missense Variant
MODERATE
ENST00000333467.4
Likely_benign
0.001767490000
rs143126732
1
1
ENST00000333467.4
Likely_benign
rs143126732
AR
chrX
67545316
67545319
TGCA
T
c.237_239del
ctGCAg/ctg
p.Q80del
0.859
7
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000374690.9
COSV65954886
.
7
3
ENST00000374690.9
COSV65954886
.
AR
chrX
67545400
67545403
GGCA
G
c.271_273del
agGCAg/agg
p.Q91del
0.042
7
6
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000374690.9
COSV65954891
rs753526329
7
6
ENST00000374690.9
COSV65954891
rs753526329
AR
chrX
67545316
67545322
TGCAGCA
T
c.234_239del
ctGCAGCAg/ctg
p.Q79_Q80del
0.132
7
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000374690.9
COSV65952724
.
7
3
ENST00000374690.9
COSV65952724
.
Total mutations showing: 478
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
Download
CNV
There are no omics data for this model.
Histology Information for Model: BL8106
There are no histology images for this model.
Metastasis Information for Model: BL8106
Patient
PDX
Abdomen
Adrenal
Colon
Kidney
Liver
Lung
Lymph Node
Pelvis
Peritoneum
Small Bowel
Patient Treatment Information for Model: BL8106
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
10
BCG
BCG +-IFN
38.53
38.64
40 days
Unknown
Unknown
15
BCG
BCG +-IFN
39.02
39.12
36 days
Progressive Disease
No response
20
BCG
BCG +-IFN
39.31
39.35
15 days
Unknown
Unknown
25
BCG
BCG +-IFN
40.25
40.29
15 days
Stable Disease
No response
40
Gemcitabine
Systemic Chemotherapy
46.62
46.62
1 day
Complete Response
Complete response
50
BCG
BCG +-IFN
48.45
48.49
15 days
Unknown
Unknown
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