RPL15

Ribosomal protein L15 P61313 RL15_HUMAN
Protein Coding Chr 3 3p24.2 Swiss-Prot reviewed Entrez 6138
Mutations
506
CL 81 · Tissue 376
Samples
73
CL 14 · Tissue 53
Peptides
73
unique mutant peptides
Transcripts
9
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
Mutations50681376
Samples731453
Peptides731351

Function

RPL15 · Ribosomal protein L15

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L15E family of ribosomal proteins and a component of the 60S subunit. This gene shares sequence similarity with the yeast ribosomal protein YL10 gene. Elevated expression of this gene has been observed in esophageal tumors and gastric cancer tissues, and deletion of this gene has been observed in a Diamond-Blackfan anemia (DBA) patient. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Mar 2017].

Isoforms & Proteins

9 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
ENST00000307839 P61313 76 59
ENST00000354811 P61313 68 56
ENST00000413699 P61313 68 56
ENST00000415719 P61313 68 56
ENST00000611050 P61313 68 56
ENST00000644185 P61313 68 56
ENST00000456530 P61313-2 46 39
ENST00000436146 E7ERA2* 22 18
ENST00000644684 E7ERA2* 22 18

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p24.2
Entrez ID
Aliases
DBA12EC45L15RPL10RPLY10RPYL10

Recurrent Mutations

All 59 amino-acid changes on canonical ENST00000307839 · 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 RPL15 · 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 RPL15 – 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
1/40 2%
0/0 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Endometrial Carcinoma
0/42 0%
3/612 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Melanoma
3/210 1%
5/1899 0%
Squamous Cell Lung Carcinoma
3/57 5%
0/810 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Colorectal Carcinoma
2/143 1%
9/3239 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
1/2534 0%
Glioma
0/52 0%
4/2127 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where RPL15 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL15 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 506 mutations in RPL15

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