RPL32

Ribosomal protein L32 P62910 RL32_HUMAN
Protein Coding Chr 3 3p25.2 Swiss-Prot reviewed Entrez 6161
Mutations
247
CL 46 · Tissue 196
Samples
62
CL 18 · Tissue 39
Peptides
54
unique mutant peptides
Transcripts
5
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
Mutations24746196
Samples621839
Peptides541439

Function

RPL32 · Ribosomal protein L32

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 L32E family of ribosomal proteins. It is located in the cytoplasm. Although some studies have mapped this gene to 3q13.3-q21, it is believed to map to 3p25-p24. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding the same protein have been observed for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000429711 P62910 56 42
ENST00000273223 F8W727* 53 43
ENST00000396953 P62910 46 37
ENST00000396957 P62910 46 37
ENST00000435983 P62910 46 37

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p25.2
Entrez ID
Aliases
L32PP9932eL32

Recurrent Mutations

All 42 amino-acid changes on canonical ENST00000429711 · 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 RPL32 · 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 RPL32 – 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
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Plasma Cell Myeloma
0/44 0%
3/305 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Colorectal Carcinoma
2/143 1%
9/3239 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Other Sarcomas
2/69 3%
0/699 0%
Pancreatic Carcinoma
3/89 3%
1/1611 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Melanoma
0/210 0%
4/1899 0%
Endometrial Carcinoma
1/42 2%
0/612 0%
Glioma
0/52 0%
3/2127 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Non-Small Cell Lung Carcinoma
2/304 1%
0/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Non-Cancerous
0/104 0%
1/830 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
1/13 8%
0/2105 0%
Other Blood Cancers
0/61 0%
1/2725 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where RPL32 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL32 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 247 mutations in RPL32

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