ESRRA

Estrogen related receptor alpha P11474 ERR1_HUMAN
Protein Coding Chr 11 11q13.1 Swiss-Prot reviewed Entrez 2101
Mutations
956
CL 118 · Tissue 825
Samples
260
CL 54 · Tissue 200
Peptides
156
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
Mutations956118825
Samples26054200
Peptides15641113

Function

ESRRA · Estrogen related receptor alpha

The protein encoded by this gene is a nuclear receptor that is most closely related to the estrogen receptor. This protein acts as a site-specific transcription factor and interacts with members of the PGC-1 family of transcription cofactors to regulate the expression of most genes involved in cellular energy production as well as in the process of mitochondrial biogenesis. A processed pseudogene of ESRRA is located on chromosome 13q12.1. [provided by RefSeq, Jun 2019].

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
ENST00000000442 P11474 412 146
ENST00000405666 P11474 328 127
ENST00000677967 P11474-2 207 67
ENST00000406310 A0A6E1WCP9* 9 8

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.1
Entrez ID
Aliases
ERR1ERRaERRalphaESRL1NR3B1

Recurrent Mutations

All 146 amino-acid changes on canonical ENST00000000442 · 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 ESRRA · 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 ESRRA – 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
10/40 25%
0/0 0%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Thyroid Gland Carcinoma
2/45 4%
23/1592 1%
Bladder Carcinoma
0/58 0%
13/956 1%
Endometrial Carcinoma
5/42 12%
3/612 0%
Colorectal Carcinoma
6/143 4%
34/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
3/154 2%
4/577 1%
Non-Small Cell Lung Carcinoma
7/304 2%
9/1390 1%
Cervical Carcinoma
2/35 6%
2/422 0%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Hepatocellular Carcinoma
1/46 2%
18/2210 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Squamous Cell Lung Carcinoma
3/57 5%
3/810 0%
Melanoma
2/210 1%
12/1899 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Mesothelioma
0/62 0%
1/165 1%
Gastric Carcinoma
0/74 0%
8/1809 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Meningioma
0/3 0%
1/252 0%
Other Sarcomas
0/69 0%
3/699 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
8/2534 0%
Prostate Carcinoma
2/13 15%
6/2105 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
Pancreatic Carcinoma
0/89 0%
5/1611 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ESRRA 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 956 mutations in ESRRA

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