UBAP2

Ubiquitin associated protein 2 Q5T6F2 UBAP2_HUMAN
Protein Coding Chr 9 9p13.3 Swiss-Prot reviewed Entrez 55833
Mutations
607
CL 106 · Tissue 483
Samples
429
CL 88 · Tissue 333
Peptides
375
unique mutant peptides
Transcripts
4
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
Mutations607106483
Samples42988333
Peptides37560306

Function

UBAP2 · Ubiquitin associated protein 2

The protein encoded by this gene contains a UBA (ubiquitin associated) domain, which is characteristic of proteins that function in the ubiquitination pathway. This gene may show increased expression in the adrenal gland and lymphatic tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013].

Isoforms & Proteins

4 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
ENST00000379238 Q5T6F2 483 337
ENST00000360802 A0A8C8MQ70* 120 84
ENST00000379239 A0A8C8KGQ8* 3 3
ENST00000682239 Q5T6F2 1 1

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9p13.3
Entrez ID
Aliases
UBAP-2

Recurrent Mutations

All 337 amino-acid changes on canonical ENST00000379238 · 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 UBAP2 · 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 UBAP2 – 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
5/40 12%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Endometrial Carcinoma
6/42 14%
20/612 3%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Colorectal Carcinoma
20/143 14%
50/3239 2%
Retinoblastoma
1/27 4%
0/30 0%
Squamous Cell Lung Carcinoma
5/57 9%
9/810 1%
Non-Small Cell Lung Carcinoma
9/304 3%
17/1390 1%
Cervical Carcinoma
0/35 0%
7/422 2%
Gastric Carcinoma
1/74 1%
27/1809 1%
Bladder Carcinoma
0/58 0%
15/956 2%
Burkitts Lymphoma
1/32 3%
2/196 1%
Melanoma
2/210 1%
24/1899 1%
Other Solid Cancers
4/94 4%
15/1515 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Ovarian Carcinoma
4/109 4%
8/998 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Hepatocellular Carcinoma
1/46 2%
22/2210 1%
Glioblastoma
1/98 1%
0/0 0%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Non-Cancerous
1/104 1%
7/830 1%
Plasma Cell Myeloma
0/44 0%
3/305 1%
Thyroid Gland Carcinoma
0/45 0%
13/1592 1%
Head and Neck Carcinoma
1/85 1%
12/1574 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Biliary Tract Carcinoma
0/54 0%
6/950 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
13/2550 1%

Mutation Distribution

Where UBAP2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in UBAP2 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 607 mutations in UBAP2

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