SART3

Spliceosome associated factor 3, U4/U6 recycling protein Q15020 SART3_HUMAN
Protein Coding Chr 12 12q23.3 Swiss-Prot reviewed Entrez 9733
Mutations
820
CL 155 · Tissue 649
Samples
393
CL 89 · Tissue 297
Peptides
332
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
Mutations820155649
Samples39389297
Peptides33260272

Function

SART3 · Spliceosome associated factor 3, U4/U6 recycling protein

The protein encoded by this gene is an RNA-binding nuclear protein that is a tumor-rejection antigen. This antigen possesses tumor epitopes capable of inducing HLA-A24-restricted and tumor-specific cytotoxic T lymphocytes in cancer patients and may be useful for specific immunotherapy. This gene product is found to be an important cellular factor for HIV-1 gene expression and viral replication. It also associates transiently with U6 and U4/U6 snRNPs during the recycling phase of the spliceosome cycle. This encoded protein is thought to be involved in the regulation of mRNA splicing. [provided by RefSeq, Jul 2008].

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
ENST00000431469 Q15020-4 355 274
ENST00000546815 Q15020 305 230
ENST00000228284 A0A499FI31* 112 78
ENST00000546611 Q15020-3 48 36

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q23.3
Entrez ID
Aliases
DSAP1P100RP11-13G14TIP110p110p110(nrb)

Recurrent Mutations

All 274 amino-acid changes on canonical ENST00000431469 · 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 SART3 · 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 SART3 – 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
6/40 15%
0/0 0%
Endometrial Carcinoma
4/42 10%
23/612 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Colorectal Carcinoma
15/143 10%
57/3239 2%
Cervical Carcinoma
0/35 0%
9/422 2%
Melanoma
4/210 2%
33/1899 2%
Non-Small Cell Lung Carcinoma
16/304 5%
13/1390 1%
Rhabdomyosarcoma
3/33 9%
0/171 0%
Plasma Cell Myeloma
4/44 9%
1/305 0%
Gastric Carcinoma
0/74 0%
26/1809 1%
Neuroendocrine Tumour
4/154 3%
3/577 1%
Other Solid Cancers
0/94 0%
14/1515 1%
Ovarian Carcinoma
4/109 4%
5/998 0%
Non-Cancerous
1/104 1%
6/830 1%
Esophageal Squamous Cell Carcinoma
7/51 14%
12/2550 0%
Hepatocellular Carcinoma
2/46 4%
14/2210 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Bladder Carcinoma
1/58 2%
6/956 1%
Glioma
4/52 8%
10/2127 0%
Thyroid Gland Carcinoma
0/45 0%
9/1592 1%
Breast Carcinoma
8/144 6%
10/3264 0%
Other Sarcomas
0/69 0%
4/699 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Burkitts Lymphoma
0/32 0%
1/196 1%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Pancreatic Carcinoma
0/89 0%
5/1611 0%
Prostate Carcinoma
0/13 0%
6/2105 0%

Mutation Distribution

Where SART3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SART3 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 820 mutations in SART3

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