RPL23A

Ribosomal protein L23a P62750 RL23A_HUMAN
Protein Coding Chr 17 17q11.2 Swiss-Prot reviewed Entrez 6147
Mutations
200
CL 42 · Tissue 157
Samples
82
CL 24 · Tissue 57
Peptides
71
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
Mutations20042157
Samples822457
Peptides711952

Function

RPL23A · Ribosomal protein L23a

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 L23P family of ribosomal proteins. It is located in the cytoplasm. The protein may be one of the target molecules involved in mediating growth inhibition by interferon. In yeast, the corresponding protein binds to a specific site on the 26S rRNA. This gene is co-transcribed with the U42A, U42B, U101A, and U101B small nucleolar RNA genes, which are located in its third, first, second, and fourth introns, respectively. 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

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
ENST00000422514 P62750 75 57
ENST00000394938 A8MUS3* 71 60
ENST00000472628 K7EMA7* 27 22
ENST00000496182 K7EMA7* 27 22

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q11.2
Entrez ID
Aliases
L23AMDA20uL23

Recurrent Mutations

All 57 amino-acid changes on canonical ENST00000422514 · 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 RPL23A · 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 RPL23A – 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
2/40 5%
0/0 0%
Glioblastoma
3/98 3%
0/0 0%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Endometrial Carcinoma
4/42 10%
8/612 1%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Mesothelioma
0/62 0%
1/165 1%
Bladder Carcinoma
1/58 2%
3/956 0%
Gastric Carcinoma
2/74 3%
5/1809 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Melanoma
2/210 1%
4/1899 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
B-Lymphoblastic Leukemia
4/55 7%
0/2640 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Other Sarcomas
1/69 1%
0/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Colorectal Carcinoma
0/143 0%
4/3239 0%
Non-Cancerous
1/104 1%
0/830 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where RPL23A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL23A 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 200 mutations in RPL23A

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