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Tmem45b Modulates itch via Endoplasmic Reticulum Calcium Regulation

GSE304359 Mus musculus (mouse) RNA-seq (gene expression) 21 samples Submitted 2026/01/01 Platform GPL28330
At a glance

RNA-seq (gene expression) · mouse · 21 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
21 samples: 11 × Mrgprd-cre mice, RNA-seq, vs 6 × DRG, Tmem45b-flox mice, RNA-seq, vs 4 × DRG, CFA model,Tmem45b-flox mice, RNA-seq,Groups 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.
Summary (written by the submitters)
Chronic itch is detected by dorsal root ganglia (DRG) that severely impairs quality of life. However, its underlying mechanisms remain poorly understood. We identified that Tmem45b was contained in natriuretic peptide type B (Nppb)-, mas-related G-protein coupled receptor member A3 (Mrgpra3)-, and Mrgprd-positive DRG neurons, which are associated with itch sensation.
Read the full summary ↓
The role of Tmem45b in itch sensation has not been explored. Tmem45b conditional knockout (cKO) mice exhibited decreased scratching to β-alanine, and increased scratching to chloroquine. Notably, Tmem45b cKO alleviated chronic itch. Furthermore, Tmem45b cKO impaired the calcium response to β-alanine and allyl isothiocyanate but not to chloroquine in dissociated DRG neurons. Tmem45b deficiency led to significant downregulation of sarco/endoplasmic reticulum calcium transport ATPase 1 (Serca1), impairing calcium storage capacity of endoplasmic reticulum (ER). Inhibition of Serca1 in DRG neurons reduced intracellular calcium release triggered by β-alanine and chloroquine. Together,Tmem45b deficiency may reduce nonhistaminergic itch and disrupt ER calcium regulation, highlighting a potential target for chronic itch therapy.
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 GSE304359_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 PRJNA1300793 and SRA study SRP606009. Searching any of these in the dataset finder brings you back here.

Study design
11 × Mrgprd-cre mice, RNA-seq, vs 6 × DRG, Tmem45b-flox mice, RNA-seq, vs 4 × DRG, CFA model,Tmem45b-flox mice, RNA-seq,

Supports a between-group comparison across 21 samples.

How we read this: 3 replicated groups read from 21 sample titles; they account for 21 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
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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.