MRPL46

Mitochondrial ribosomal protein L46 Q9H2W6 RM46_HUMAN
Protein Coding Chr 15 15q25.3 Swiss-Prot reviewed Entrez 26589
Mutations
185
CL 52 · Tissue 128
Samples
121
CL 38 · Tissue 80
Peptides
101
unique mutant peptides
Transcripts
2
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
Mutations18552128
Samples1213880
Peptides1012876

Function

MRPL46 · Mitochondrial ribosomal protein L46

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. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000312475 Q9H2W6 123 95
ENST00000558531 A0A087WT90* 62 55

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q25.3
Entrez ID
Aliases
C15orf4LIECG2P2ECSLmL46

Recurrent Mutations

All 95 amino-acid changes on canonical ENST00000312475 · 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 MRPL46 · 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 MRPL46 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
3/42 7%
5/612 1%
Glioblastoma
1/98 1%
0/0 0%
Colorectal Carcinoma
12/143 8%
19/3239 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Melanoma
2/210 1%
8/1899 0%
Non-Small Cell Lung Carcinoma
4/304 1%
4/1390 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
0/104 0%
3/830 0%
Glioma
0/52 0%
6/2127 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Gastric Carcinoma
1/74 1%
3/1809 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Neuroblastoma
1/87 1%
1/1331 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
1/2534 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Breast Carcinoma
1/144 1%
1/3264 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Other Blood Cancers
1/61 2%
0/2725 0%

Mutation Distribution

Where MRPL46 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MRPL46 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 185 mutations in MRPL46

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