RPL3

Ribosomal protein L3 P39023 RL3_HUMAN
Protein Coding Chr 22 22q13.1 Swiss-Prot reviewed Entrez 6122
Mutations
262
CL 56 · Tissue 201
Samples
140
CL 36 · Tissue 101
Peptides
119
unique mutant peptides
Transcripts
2
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
Mutations26256201
Samples14036101
Peptides1192698

Function

RPL3 · Ribosomal protein L3

Ribosomes, the complexes that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L3P family of ribosomal proteins and it is located in the cytoplasm. The protein can bind to the HIV-1 TAR mRNA, and it has been suggested that the protein contributes to tat-mediated transactivation. This gene is co-transcribed with several small nucleolar RNA genes, which are located in several of this gene's introns. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000216146 P39023 149 117
ENST00000401609 G5E9G0* 113 95

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q13.1
Entrez ID
Aliases
ASC-1L3TARBP-BuL3

Recurrent Mutations

All 117 amino-acid changes on canonical ENST00000216146 · 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 RPL3 · 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 RPL3 – 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
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Endometrial Carcinoma
3/42 7%
5/612 1%
Ewings Sarcoma
3/63 5%
0/262 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Colorectal Carcinoma
10/143 7%
17/3239 1%
Melanoma
3/210 1%
13/1899 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Bladder Carcinoma
2/58 3%
3/956 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Non-Small Cell Lung Carcinoma
4/304 1%
3/1390 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Non-Cancerous
0/104 0%
3/830 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Kidney Carcinoma
0/85 0%
5/1862 0%
Other Solid Cancers
0/94 0%
4/1515 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
5/2534 0%
Pancreatic Carcinoma
1/89 1%
2/1611 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Other Sarcomas
0/69 0%
1/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Glioma
0/52 0%
2/2127 0%
Breast Carcinoma
0/144 0%
3/3264 0%
Prostate Carcinoma
1/13 8%
1/2105 0%

Mutation Distribution

Where RPL3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL3 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 262 mutations in RPL3

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