RPL36

Ribosomal protein L36 Q9Y3U8 RL36_HUMAN
Protein Coding Chr 19 19p13.3 Swiss-Prot reviewed Entrez 25873
Mutations
116
CL 21 · Tissue 95
Samples
33
CL 12 · Tissue 21
Peptides
32
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
Mutations1162195
Samples331221
Peptides321220

Function

RPL36 · Ribosomal protein L36

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 L36E family of ribosomal proteins. It is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they 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

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
ENST00000347512 Q9Y3U8 32 27
ENST00000394580 Q9Y3U8 22 18
ENST00000577222 Q9Y3U8 22 18
ENST00000579649 Q9Y3U8 22 18
ENST00000579446 J3QSB5* 18 14

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.3
Entrez ID
Aliases
L36eL36

Recurrent Mutations

All 27 amino-acid changes on canonical ENST00000347512 · 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 RPL36 · 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 RPL36 – 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-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Endometrial Carcinoma
3/42 7%
0/612 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Head and Neck Carcinoma
1/85 1%
2/1574 0%
Glioma
0/52 0%
3/2127 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Colorectal Carcinoma
0/143 0%
3/3239 0%
Melanoma
1/210 0%
1/1899 0%
Breast Carcinoma
1/144 1%
2/3264 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
0/2534 0%
Neuroblastoma
1/87 1%
0/1331 0%
Gastric Carcinoma
0/74 0%
1/1809 0%

Mutation Distribution

Where RPL36 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RPL36 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 116 mutations in RPL36

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