MRPL43

Mitochondrial ribosomal protein L43 Q8N983 RM43_HUMAN
Protein Coding Chr 10 10q24.31 Swiss-Prot reviewed Entrez 84545
Mutations
452
CL 46 · Tissue 361
Samples
95
CL 14 · Tissue 80
Peptides
146
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
Mutations45246361
Samples951480
Peptides14614105

Function

MRPL43 · Mitochondrial ribosomal protein L43

Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. This gene and the gene for a semaphorin class 4 protein (SEMA4G) overlap at map location 10q24.31 and are transcribed in opposite directions. Sequence analysis identified multiple transcript variants encoding at least four different protein isoforms. [provided by RefSeq, Jul 2008].

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
ENST00000370242 Q8N983-7 81 74
ENST00000342071 Q8N983-6 76 68
ENST00000318325 Q8N983 57 51
ENST00000299179 Q8N983-2 55 47
ENST00000370241 B1AL05* 50 44
ENST00000318364 Q8N983-4 47 37
ENST00000370236 Q8N983-4 40 34
ENST00000370234 Q8N983-3 39 33
ENST00000477279 M0R051* 7 7

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q24.31
Entrez ID
Aliases
L43mtMRP-L43bMRP36amL43

Recurrent Mutations

All 74 amino-acid changes on canonical ENST00000370242 · 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 MRPL43 · 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 MRPL43 – 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%
Endometrial Carcinoma
0/42 0%
5/612 1%
Melanoma
0/210 0%
14/1899 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Ovarian Carcinoma
3/109 3%
1/998 0%
Non-Small Cell Lung Carcinoma
2/304 1%
4/1390 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Colorectal Carcinoma
1/143 1%
8/3239 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Non-Cancerous
0/104 0%
2/830 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Neuroblastoma
2/87 2%
0/1331 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Glioma
0/52 0%
2/2127 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Other Blood Cancers
0/61 0%
1/2725 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where MRPL43 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MRPL43 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 452 mutations in MRPL43

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