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RNA-seq of ex vivo differentiated osteoclasts of FLT3 ITD Ptprc KO mice and controls

GSE273708 Mus musculus (mouse) RNA-seq (gene expression) 16 samples Submitted 2025/02/12 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 16 samples

What it is
RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
Organism
Mus musculus (mouse)
Samples
16 samples: 4 × WT vs 4 × Ptprc KO vs 4 × FLT3 ITD vs 4 × FLT3 ITD Ptprc KOGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Oncogenic FLT3 internal tandem duplications (ITD) and CD45/PTPRC control osteoclast functions and bone microarchitectureJBMR plus · 2025
Summary (written by the submitters)
The receptor tyrosine kinase FLT3 is expressed in myeloid and lymphoid progenitor cells. Here, the influence of the FLT3 ITD mutation and PTPRC inactivation on the bone remodeling was studied in mice. Gene expression analysis of differentiated osteoclasts showed dysregulated signaling pathways influencing their differentiation as well as the coupling of bone resorption and formation.
Published in
Oncogenic FLT3 internal tandem duplications (ITD) and CD45/PTPRC control osteoclast functions and bone microarchitecture
Lossius-Cott C, Annoh A, Bens M et al. · JBMR plus 2025 · PMID 39906260 · doi:10.1093/jbmrpl/ziae173
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE273708_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.

Also filed as BioProject PRJNA1142895 and SRA study SRP523585. Searching any of these in the dataset finder brings you back here.

Study design
4 × WT vs 4 × Ptprc KO vs 4 × FLT3 ITD vs 4 × FLT3 ITD Ptprc KO

Supports a between-group comparison across 16 samples.

How we read this: 4 replicated groups read from 16 sample titles; they account for 16 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

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