MassIVE MSV000092189

Complete Public PXD043055

WNT2B is required for development and function of human intestine

Description

The experiment goal was to identify differentially expressed proteins associated with WNT2B mutation p.R69* in human intestinal epithelia. Skin fibroblasts from a patient with the mutation were used to establish human intestinal organoids (HIOs). The hESC H1 cell line was used to generate wild-type WNT2B HIOs for comparison. The HIOs were transplanted into mice to promote maturation for 8 weeks, followed by dissection and crypt isolation to seed ex vivo epithelial (enteroid) cultures. The enteroid cultures were harvested for analysis by tandem mass tag spectrometry. [doi:10.25345/C5K931H1N] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: WNT2B intestinal organoid enteroid epithelia

Contact

Principal Investigators:
(in alphabetical order)
Jennifer Foulke-Abel, Johns Hopkins University School of Medicine, United States
Submitting User: jfoulke
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Owner Reanalyses
Experimental Design
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Identification Results
    Proteins (Human, Remapped):
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Quantification Results
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Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

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Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

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Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

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Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

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Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.