EARS2

Glutamyl-tRNA synthetase 2, mitochondrial Q5JPH6 SYEM_HUMAN
Protein Coding Chr 16 16p12.2 Swiss-Prot reviewed Entrez 124454
Mutations
692
CL 90 · Tissue 598
Samples
255
CL 52 · Tissue 201
Peptides
210
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
Mutations69290598
Samples25552201
Peptides21041172

Function

EARS2 · Glutamyl-tRNA synthetase 2, mitochondrial

This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of glutamate to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 12 (COXPD12). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015].

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
ENST00000449606 Q5JPH6 263 193
ENST00000563232 Q5JPH6-2 217 166
ENST00000564501 H3BTB7* 212 161

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p12.2
Entrez ID
Aliases
COXPD12MSE1gluRSmtGlnRSmtGluRS

Recurrent Mutations

All 193 amino-acid changes on canonical ENST00000449606 · 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 EARS2 · 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 EARS2 – 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%
5/133 4%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Endometrial Carcinoma
2/42 5%
11/612 2%
Burkitts Lymphoma
0/32 0%
4/196 2%
Melanoma
6/210 3%
22/1899 1%
Neuroendocrine Tumour
5/154 3%
3/577 1%
Non-Small Cell Lung Carcinoma
6/304 2%
12/1390 1%
Colorectal Carcinoma
7/143 5%
27/3239 1%
Squamous Cell Lung Carcinoma
1/57 2%
7/810 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Plasma Cell Myeloma
0/44 0%
3/305 1%
Bladder Carcinoma
2/58 3%
6/956 1%
Other Solid Cancers
1/94 1%
11/1515 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Breast Carcinoma
7/144 5%
17/3264 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Head and Neck Carcinoma
0/85 0%
10/1574 1%
Gastric Carcinoma
1/74 1%
9/1809 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Other Sarcomas
1/69 1%
3/699 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Esophageal Carcinoma
0/23 0%
3/769 0%
Glioma
1/52 2%
6/2127 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
7/2550 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
5/2534 0%
Thyroid Gland Carcinoma
1/45 2%
2/1592 0%

Mutation Distribution

Where EARS2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in EARS2 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 692 mutations in EARS2

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