ETFA

Electron transfer flavoprotein subunit alpha P13804 ETFA_HUMAN
Protein Coding Chr 15 15q24.2-q24.3 Swiss-Prot reviewed Entrez 2108
Mutations
312
CL 44 · Tissue 267
Samples
123
CL 20 · Tissue 102
Peptides
101
unique mutant peptides
Transcripts
4
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
Mutations31244267
Samples12320102
Peptides1011587

Function

ETFA · Electron transfer flavoprotein subunit alpha

ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

4 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
ENST00000557943 P13804 124 85
ENST00000433983 P13804-2 97 70
ENST00000559602 H0YK49* 70 54
ENST00000560726 H0YL83* 21 18

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q24.2-q24.3
Entrez ID
Aliases
EMAGA2MADD

Recurrent Mutations

All 85 amino-acid changes on canonical ENST00000557943 · 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 ETFA · 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 ETFA – 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
2/42 5%
9/612 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Other Solid Cancers
0/94 0%
16/1515 1%
Melanoma
5/210 2%
11/1899 1%
Colorectal Carcinoma
2/143 1%
19/3239 1%
Squamous Cell Lung Carcinoma
3/57 5%
2/810 0%
Bladder Carcinoma
0/58 0%
5/956 1%
Medulloblastoma
0/0 0%
2/450 0%
Prostate Carcinoma
2/13 15%
4/2105 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Ovarian Carcinoma
0/109 0%
3/998 0%
Non-Small Cell Lung Carcinoma
1/304 0%
3/1390 0%
Non-Cancerous
0/104 0%
2/830 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Hepatocellular Carcinoma
1/46 2%
3/2210 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Glioma
0/52 0%
3/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Breast Carcinoma
0/144 0%
3/3264 0%
Neuroblastoma
0/87 0%
1/1331 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ETFA 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 312 mutations in ETFA

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