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Patient ID
176247
Open Patient
Specimen ID
063-R
Open Specimen
Sample ID
J2-PDC
Disease Body Location
Digestive/Gastrointestinal
OncoTree Code
COAD
CTEP SDC Code
10009951 - Adenocarcinoma - colon
PDM Type
PDC: Mixed Tumor Culture
Required Media
Complete DMEM/F12
Culture Origin
PDX-Derived Organoid
FACS
Characterization
mMHC-, hHLA+, mCD9-, hCD9+; hEpCAM+, hCD90-, hCD24+
Growth Properties
Adherent Monolayer
Proliferation Rate
in Complete Media
65 hrs
Sub-culture
Recommendations
Split ratio: 1:3 to 1:4
Culture Derivation
Prepared from a PDX-derived organoid culture. Determined to be a tumor by FACS analysis, QRT-PCR, cell morphology, and positive tumorigenicity.
Tumorigenic in
NSG Mice
Yes
No
Spheroid Growth
Yes
No
Spheroid Growth
Notes
Soft Agar Growth
Yes
No
Soft Agar
Growth Notes
Fibroblast qRT-PCR
C1 Corr
-0.39
Fibroblast qRT-PCR
C2 Corr
-0.45
Fibroblast qRT-PCR
Top Hits
EPCAM,KRT8,CD24,KRT18,KRT19
Images (if available)
In Vitro Images
View
Image Type
Notes
In Vitro Image
Light Microscopy
20x magnification, Passage 32
Xenograft from In Vitro Culture
20X image of cell culture-derived xenograft
Export
Genomic Analysis
External Genetic Analysis Data
A data file is available if a Download link is displayed:
Somatic Mutations Associated with Cancer (*.vcf and *.maf)
Whole Exome Sequencing (*.vcf)
Download
Ver:
2.0.2.51.0
Whole Exome FASTQ (*.FASTQ.gz; for paired-end sequence, download both files)
Download Read1 FASTQ
Download Read2 FASTQ
Ver:
2.0.2.51.0
RNASeq FASTQ (*.FASTQ.gz; for paired-end sequence, download both files)
Download Read1 FASTQ
Download Read2 FASTQ
Ver:
2.0.2.21.0
RNASeq Transcripts per Million (TPM; *.RSEM.genes.results and *.RSEM.isoforms.results tab-delimited text file)
Download RSEM (genes)
Download RSEM (isoforms)
Ver:
2.0.2.21.0
OncoKB Gene Panel
View
Hugo
Symbol
HGVS Protein
Change
Variant Allele
Frequency
Total
Reads
Variant
Class
Oncogenicity
Predicted
Functional Effect
OncoKB
Version
APC
p.T1368Kfs*4
1.0000
101
Frame_Shift_Del
Likely Oncogenic
Likely Loss-of-function
v7.1
TP53
p.R175H
1.0000
169
Missense_Mutation
Oncogenic
Loss-of-function
v7.1
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