POLR3E

RNA polymerase III subunit E Q9NVU0 RPC5_HUMAN
Protein Coding Chr 16 16p12.2 Swiss-Prot reviewed Entrez 55718
Mutations
1,475
CL 203 · Tissue 1,256
Samples
338
CL 76 · Tissue 257
Peptides
295
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
Mutations1,4752031,256
Samples33876257
Peptides29557239

Function

POLR3E · RNA polymerase III subunit E

Predicted to enable DNA-directed 5'-3' RNA polymerase activity. Predicted to be involved in defense response to virus; innate immune response; and transcription, DNA-templated. Located in nucleoplasm. Part of RNA polymerase III complex. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000299853 Q9NVU0 355 272
ENST00000418581 Q9NVU0-5 283 232
ENST00000564209 Q9NVU0-4 281 237
ENST00000615879 A0A0C4DH01* 279 229
ENST00000359210 Q9NVU0-2 277 233

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p12.2
Entrez ID
Aliases
C37RPC5SIN

Recurrent Mutations

All 272 amino-acid changes on canonical ENST00000299853 · 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 POLR3E · 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 POLR3E – 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%
Endometrial Carcinoma
8/42 19%
14/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Colorectal Carcinoma
18/143 13%
57/3239 2%
Melanoma
0/210 0%
37/1899 2%
Cervical Carcinoma
0/35 0%
6/422 1%
Gastric Carcinoma
3/74 4%
19/1809 1%
Squamous Cell Lung Carcinoma
4/57 7%
6/810 1%
Chondrosarcoma
1/14 7%
0/75 0%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Non-Small Cell Lung Carcinoma
10/304 3%
6/1390 0%
Other Sarcomas
1/69 1%
5/699 1%
Meningioma
1/3 33%
1/252 0%
Thyroid Gland Carcinoma
1/45 2%
11/1592 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Bladder Carcinoma
0/58 0%
7/956 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Head and Neck Carcinoma
1/85 1%
9/1574 1%
Other Solid Cancers
1/94 1%
8/1515 1%
Non-Cancerous
2/104 2%
3/830 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Hepatocellular Carcinoma
0/46 0%
11/2210 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Glioma
0/52 0%
8/2127 0%
Ovarian Carcinoma
2/109 2%
2/998 0%
Pancreatic Carcinoma
1/89 1%
5/1611 0%
Breast Carcinoma
4/144 3%
8/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
8/2550 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Kidney Carcinoma
0/85 0%
5/1862 0%

Mutation Distribution

Where POLR3E is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in POLR3E 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 1,475 mutations in POLR3E

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