YJU2

YJU2 splicing factor homolog Q9BW85 YJU2_HUMAN
Protein Coding Chr 19 19p13.3 Swiss-Prot reviewed Entrez 55702
Mutations
137
CL 28 · Tissue 108
Samples
132
CL 27 · Tissue 104
Peptides
103
unique mutant peptides
Transcripts
1
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
Mutations13728108
Samples13227104
Peptides1032185

Function

YJU2 · YJU2 splicing factor homolog

Predicted to enable metal ion binding activity. Predicted to be involved in RNA splicing and negative regulation of DNA damage response, signal transduction by p53 class mediator. Part of U2-type catalytic step 1 spliceosome. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

1 transcript · 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
ENST00000262962 Q9BW85 137 103

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.3
Entrez ID
Aliases
CCDC94

Recurrent Mutations

All 103 amino-acid changes on canonical ENST00000262962 · 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 YJU2 · 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 YJU2 – 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
2/40 5%
0/0 0%
Unknown
0/10 0%
1/29 3%
Endometrial Carcinoma
1/42 2%
7/612 1%
Cervical Carcinoma
2/35 6%
1/422 0%
Melanoma
1/210 0%
12/1899 1%
Ovarian Carcinoma
4/109 4%
2/998 0%
Colorectal Carcinoma
1/143 1%
16/3239 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Non-Small Cell Lung Carcinoma
4/304 1%
4/1390 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Neuroendocrine Tumour
3/154 2%
0/577 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Non-Cancerous
1/104 1%
2/830 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
6/2550 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Hepatocellular Carcinoma
1/46 2%
4/2210 0%
Breast Carcinoma
3/144 2%
4/3264 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
2/2534 0%
Neuroblastoma
0/87 0%
2/1331 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Glioma
0/52 0%
2/2127 0%
Prostate Carcinoma
0/13 0%
2/2105 0%

Mutation Distribution

Where YJU2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in YJU2 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.

Mutations

All 137 mutations in YJU2

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