RELA

RELA proto-oncogene, NF-kB subunit Q04206 TF65_HUMAN
Protein Coding Chr 11 11q13.1 Swiss-Prot reviewed Entrez 5970
Mutations
895
CL 123 · Tissue 760
Samples
277
CL 57 · Tissue 215
Peptides
216
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
Mutations895123760
Samples27757215
Peptides21641177

Function

RELA · RELA proto-oncogene, NF-kB subunit

NF-kappa-B is a ubiquitous transcription factor involved in several biological processes. It is held in the cytoplasm in an inactive state by specific inhibitors. Upon degradation of the inhibitor, NF-kappa-B moves to the nucleus and activates transcription of specific genes. NF-kappa-B is composed of NFKB1 or NFKB2 bound to either REL, RELA, or RELB. The most abundant form of NF-kappa-B is NFKB1 complexed with the product of this gene, RELA. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011].

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
ENST00000406246 Q04206 287 191
ENST00000308639 Q04206-4 241 172
ENST00000612991 A0A087X0W8* 196 149
ENST00000525693 F6T8P2* 171 129

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.1
Entrez ID
Aliases
AIF3BL3CMCUNFKB3p65

Recurrent Mutations

All 191 amino-acid changes on canonical ENST00000406246 · 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 RELA · 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 RELA – 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
4/40 10%
0/0 0%
Endometrial Carcinoma
8/42 19%
16/612 3%
Other Solid Cancers
0/94 0%
41/1515 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Burkitts Lymphoma
3/32 9%
1/196 1%
Melanoma
8/210 4%
22/1899 1%
Cervical Carcinoma
2/35 6%
4/422 1%
Gastric Carcinoma
4/74 5%
17/1809 1%
Ovarian Carcinoma
6/109 6%
6/998 1%
Colorectal Carcinoma
8/143 6%
28/3239 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
7/810 1%
Other Sarcomas
2/69 3%
4/699 1%
Medulloblastoma
0/0 0%
3/450 1%
Non-Small Cell Lung Carcinoma
3/304 1%
8/1390 1%
Mesothelioma
0/62 0%
1/165 1%
Meningioma
0/3 0%
1/252 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
6/2550 0%
Breast Carcinoma
0/144 0%
9/3264 0%
Thyroid Gland Carcinoma
2/45 4%
2/1592 0%
Glioma
0/52 0%
5/2127 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
6/2534 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Prostate Carcinoma
0/13 0%
3/2105 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in RELA 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 895 mutations in RELA

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