UBE2J2

Ubiquitin conjugating enzyme E2 J2 Q8N2K1 UB2J2_HUMAN
Protein Coding Chr 1 1p36.33 Swiss-Prot reviewed Entrez 118424
Mutations
640
CL 90 · Tissue 549
Samples
150
CL 30 · Tissue 119
Peptides
121
unique mutant peptides
Transcripts
5
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
Mutations64090549
Samples15030119
Peptides12117104

Function

UBE2J2 · Ubiquitin conjugating enzyme E2 J2

The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is located in the membrane of the endoplasmic reticulum. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000349431 Q8N2K1 153 106
ENST00000400930 Q8N2K1-3 141 106
ENST00000360466 Q8N2K1 138 103
ENST00000347370 A6NGS0* 104 80
ENST00000400929 A6NGS0* 104 80

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p36.33
Entrez ID
Aliases
NCUBE-2NCUBE2PRO2121UBC6

Recurrent Mutations

All 106 amino-acid changes on canonical ENST00000349431 · 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 UBE2J2 · 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 UBE2J2 – 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
Glioblastoma
4/98 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
7/42 17%
4/612 1%
Melanoma
5/210 2%
17/1899 1%
Colorectal Carcinoma
5/143 4%
21/3239 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Non-Small Cell Lung Carcinoma
3/304 1%
4/1390 0%
Neuroendocrine Tumour
0/154 0%
3/577 1%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
7/2550 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Medulloblastoma
0/0 0%
1/450 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Glioma
2/52 4%
2/2127 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Breast Carcinoma
1/144 1%
4/3264 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Bladder Carcinoma
0/58 0%
1/956 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

Where UBE2J2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in UBE2J2 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 640 mutations in UBE2J2

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