RPL14

Ribosomal protein L14 P50914 RL14_HUMAN
Protein Coding Chr 3 3p22.1 Swiss-Prot reviewed Entrez 9045
Mutations
169
CL 25 · Tissue 143
Samples
73
CL 15 · Tissue 57
Peptides
69
unique mutant peptides
Transcripts
3
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
Mutations16925143
Samples731557
Peptides691157

Function

RPL14 · Ribosomal protein L14

Ribosomes, the organelles 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 L14E family of ribosomal proteins. It contains a basic region-leucine zipper (bZIP)-like domain. The protein is located in the cytoplasm. This gene contains a trinucleotide (GCT) repeat tract whose length is highly polymorphic; these triplet repeats result in a stretch of alanine residues in the encoded protein. Transcript variants utilizing alternative polyA signals and alternative 5'-terminal exons exist but all encode the same protein. 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

3 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
ENST00000396203 P50914 72 62
ENST00000338970 P50914 66 59
ENST00000416518 E7EPB3* 31 30

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p22.1
Entrez ID
Aliases
CAG-ISL-7CTG-B33L14RL14eL14hRL14

Recurrent Mutations

All 62 amino-acid changes on canonical ENST00000396203 · 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 RPL14 · 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 RPL14 – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Endometrial Carcinoma
2/42 5%
4/612 1%
Colorectal Carcinoma
3/143 2%
16/3239 0%
Non-Small Cell Lung Carcinoma
1/304 0%
4/1390 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Melanoma
0/210 0%
6/1899 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Medulloblastoma
0/0 0%
1/450 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Glioma
0/52 0%
3/2127 0%
Other Sarcomas
0/69 0%
1/699 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Breast Carcinoma
2/144 1%
1/3264 0%
Prostate Carcinoma
1/13 8%
1/2105 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Neuroblastoma
1/87 1%
0/1331 0%
Thyroid Gland Carcinoma
0/45 0%
1/1592 0%
Gastric Carcinoma
0/74 0%
1/1809 0%

Mutation Distribution

Where RPL14 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL14 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 169 mutations in RPL14

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