COX7A2L

Cytochrome c oxidase subunit 7A2 like O14548 CO72L_HUMAN
Protein Coding Chr 2 2p21 Swiss-Prot reviewed Entrez 9167
Mutations
82
CL 12 · Tissue 68
Samples
38
CL 7 · Tissue 30
Peptides
36
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
Mutations821268
Samples38730
Peptides36628

Function

COX7A2L · Cytochrome c oxidase subunit 7A2 like

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein similar to polypeptides 1 and 2 of subunit VIIa in the C-terminal region, and also highly similar to the mouse Sig81 protein sequence. This gene is expressed in all tissues, and upregulated in a breast cancer cell line after estrogen treatment. It is possible that this gene represents a regulatory subunit of COX and mediates the higher level of energy production in target cells by estrogen. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016].

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
ENST00000234301 O14548 35 32
ENST00000378669 O14548 29 28
ENST00000463055 E5RJZ1* 18 17

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p21
Entrez ID
Aliases
COX7ARCOX7RPEB1SCAF1SCAFISIG81

Recurrent Mutations

All 32 amino-acid changes on canonical ENST00000234301 · 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 COX7A2L · 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 COX7A2L – 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
Cervical Carcinoma
0/35 0%
2/422 0%
Meningioma
1/3 33%
0/252 0%
Melanoma
2/210 1%
6/1899 0%
Endometrial Carcinoma
0/42 0%
2/612 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Breast Carcinoma
2/144 1%
1/3264 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Gastric Carcinoma
1/74 1%
0/1809 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where COX7A2L is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in COX7A2L 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 82 mutations in COX7A2L

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