ECI2

Enoyl-CoA delta isomerase 2 O75521 ECI2_HUMAN
Protein Coding Chr 6 6p25.2 Swiss-Prot reviewed Entrez 10455
Mutations
637
CL 77 · Tissue 542
Samples
172
CL 28 · Tissue 136
Peptides
136
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
Mutations63777542
Samples17228136
Peptides13619117

Function

ECI2 · Enoyl-CoA delta isomerase 2

This gene encodes a member of the hydratase/isomerase superfamily. The protein encoded is a key mitochondrial enzyme involved in beta-oxidation of unsaturated fatty acids. It catalyzes the transformation of 3-cis and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-, mono-, and polyunsaturated fatty acids to the 2-trans-enoyl-CoA intermediates. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011].

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
ENST00000380118 O75521 181 132
ENST00000380125 A0A0C4DGA2* 154 112
ENST00000361538 A0A0C4DGA2* 151 111
ENST00000465828 A0A0C4DGA2* 151 111

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p25.2
Entrez ID
Aliases
ACBD2DRS-1DRS1HCA88PECIdJ1013A10.3

Recurrent Mutations

All 132 amino-acid changes on canonical ENST00000380118 · 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 ECI2 · 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 ECI2 – 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-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Endometrial Carcinoma
3/42 7%
9/612 1%
Melanoma
1/210 0%
25/1899 1%
Bladder Carcinoma
0/58 0%
12/956 1%
Mesothelioma
0/62 0%
2/165 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Colorectal Carcinoma
4/143 3%
22/3239 1%
Head and Neck Carcinoma
4/85 5%
6/1574 0%
Non-Small Cell Lung Carcinoma
2/304 1%
7/1390 0%
Gastric Carcinoma
0/74 0%
10/1809 1%
Meningioma
0/3 0%
1/252 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Biliary Tract Carcinoma
1/54 2%
1/950 0%
Other Blood Cancers
2/61 3%
3/2725 0%
B-Lymphoblastic Leukemia
1/55 2%
3/2640 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
3/2550 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Thyroid Gland Carcinoma
1/45 2%
1/1592 0%
Non-Cancerous
0/104 0%
1/830 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
Neuroblastoma
0/87 0%
1/1331 0%
Breast Carcinoma
2/144 1%
0/3264 0%

Mutation Distribution

Where ECI2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ECI2 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 637 mutations in ECI2

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