MRPS7

Mitochondrial ribosomal protein S7 Q9Y2R9 RT07_HUMAN
Protein Coding Chr 17 17q25.1 Swiss-Prot reviewed Entrez 51081
Mutations
250
CL 46 · Tissue 202
Samples
119
CL 27 · Tissue 90
Peptides
94
unique mutant peptides
Transcripts
3
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
Mutations25046202
Samples1192790
Peptides942173

Function

MRPS7 · Mitochondrial ribosomal protein S7

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 28S subunit protein. In the prokaryotic ribosome, the comparable protein is thought to play an essential role in organizing the 3' domain of the 16 S rRNA in the vicinity of the P- and A-sites. Pseudogenes corresponding to this gene are found on chromosomes 8p and 12p. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

3 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
ENST00000245539 Q9Y2R9 108 77
ENST00000579002 J3QLS3* 76 68
ENST00000579761 J3QKW2* 66 47

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q25.1
Entrez ID
Aliases
COXPD34MRP-SMRP-S7RP-S7RPMS7S7mt

Recurrent Mutations

All 77 amino-acid changes on canonical ENST00000245539 · 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 MRPS7 · 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 MRPS7 – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
7/612 1%
Ewings Sarcoma
2/63 3%
1/262 0%
Cervical Carcinoma
1/35 3%
3/422 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Bladder Carcinoma
1/58 2%
6/956 1%
Melanoma
2/210 1%
12/1899 1%
Colorectal Carcinoma
5/143 4%
12/3239 0%
Other Solid Cancers
4/94 4%
4/1515 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Mesothelioma
0/62 0%
1/165 1%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Breast Carcinoma
3/144 2%
6/3264 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Medulloblastoma
0/0 0%
1/450 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Non-Cancerous
2/104 2%
0/830 0%
Glioma
0/52 0%
4/2127 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Thyroid Gland Carcinoma
0/45 0%
1/1592 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where MRPS7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MRPS7 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 250 mutations in MRPS7

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