USO1

USO1 vesicle transport factor O60763 USO1_HUMAN
Protein Coding Chr 4 4q21.1 Swiss-Prot reviewed Entrez 8615
Mutations
586
CL 122 · Tissue 458
Samples
295
CL 79 · Tissue 211
Peptides
244
unique mutant peptides
Transcripts
2
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations586122458
Samples29579211
Peptides24453188

Function

USO1 · USO1 vesicle transport factor

The protein encoded by this gene is a peripheral membrane protein which recycles between the cytosol and the Golgi apparatus during interphase. It is regulated by phosphorylation: dephosphorylated protein associates with the Golgi membrane and dissociates from the membrane upon phosphorylation. Ras-associated protein 1 recruits this protein to coat protein complex II (COPII) vesicles during budding from the endoplasmic reticulum, where it interacts with a set of COPII vesicle-associated SNAREs to form a cis-SNARE complex that promotes targeting to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014].

Isoforms & Proteins

2 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000514213 O60763 318 237
ENST00000264904 O60763-2 268 214

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q21.1
Entrez ID
Aliases
P115TAPVDP

Recurrent Mutations

All 237 amino-acid changes on canonical ENST00000514213 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in USO1 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in USO1 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Endometrial Carcinoma
11/42 26%
15/612 2%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Melanoma
6/210 3%
32/1899 2%
Non-Small Cell Lung Carcinoma
17/304 6%
12/1390 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Bladder Carcinoma
3/58 5%
8/956 1%
Colorectal Carcinoma
6/143 4%
29/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Thyroid Gland Carcinoma
2/45 4%
14/1592 1%
Squamous Cell Lung Carcinoma
3/57 5%
5/810 1%
Mesothelioma
2/62 3%
0/165 0%
Other Solid Cancers
0/94 0%
12/1515 1%
Gastric Carcinoma
3/74 4%
11/1809 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Neuroendocrine Tumour
4/154 3%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Breast Carcinoma
2/144 1%
19/3264 1%
Ovarian Carcinoma
2/109 2%
4/998 0%
Medulloblastoma
0/0 0%
2/450 0%
Head and Neck Carcinoma
2/85 2%
5/1574 0%
Glioma
0/52 0%
8/2127 0%
Hepatocellular Carcinoma
2/46 4%
5/2210 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Other Sarcomas
0/69 0%
2/699 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Non-Cancerous
0/104 0%
2/830 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
4/2534 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
3/2550 0%

Mutation Distribution

Where USO1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in USO1 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 586 mutations in USO1

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide