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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene Breakpoints

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Tumorigenic MoA (Mechanism of Action) Scenarios of Fusion Geness

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Fusion Genomic Features

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Fusion Gene ORF Annotations

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Fusion Protein Retained/Non-Retained Functional Features

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Fusion Transcript Sequences

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Fusion Protein Sequences

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Personalized Fusion Protein Sequences

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Fusion Gene Expressed Samples

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Related Drugs

Fusion gene:EML4_COX7A2L (FusionGDB2 ID:HG27436TG9167)

Fusion Gene Summary for EML4_COX7A2L

check button Fusion gene summary
Fusion gene informationFusion gene name: EML4_COX7A2L
Fusion gene ID: hg27436tg9167
HgeneTgene
Gene symbol

EML4

COX7A2L

Gene ID

27436

9167

Gene nameEMAP like 4cytochrome c oxidase subunit 7A2 like
SynonymsC2orf2|ELP120|EMAP-4|EMAPL4|ROPP120COX7AR|COX7RP|EB1|SCAF1|SCAFI|SIG81
Cytomap

2p21

2p21

Type of geneprotein-codingprotein-coding
Descriptionechinoderm microtubule-associated protein-like 4echinoderm microtubule associated protein like 4restrictedly overexpressed proliferation-associated proteinropp 120cytochrome c oxidase subunit 7A-related protein, mitochondrialCOX7a-related proteincytochrome c oxidase subunit VII-related proteincytochrome c oxidase subunit VIIa polypeptide 2 likecytochrome c oxidase subunit VIIa-related proteinestrogen receptor
Modification date2024041120240305
UniProtAcc

Q9HC35

.
Ensembl transtripts involved in fusion geneENST00000482660, ENST00000318522, 
ENST00000401738, ENST00000402711, 
ENST00000453191, 
Fusion gene scores* DoF score* DoF score (Degree of Frequency) = # partners X # break points X # disease types
22 X 193 X 35=148610
* DoF score (Degree of Frequency) = # partners X # break points X # disease types
3 X 8 X 8=192
# samples 293164
** MAII score** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)
log2(293/148610*10)=-5.66448672354073
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)
log2(164/192*10)=3.09451759878429
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: EML4 [Title/Abstract] AND COX7A2L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEML4(42396776)-COX7A2L(42580483), # samples:2


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Fusion Gene Breakpoints for EML4_COX7A2L


check button RNA-seq based exon junction arranged fusion gene breakpoints from 8 resources (TCGA, CCLE, cBioPortal, GenBank, ChimerDB, ChimerKB, ChildHoodFusions, and GTEx). For the expressed sample information, go to Fusion Gene Sample section.
HgeneHchrHbpTgeneTchrTbp
EML4chr242396776COX7A2Lchr242580483
EML4chr242531691COX7A2Lchr242561009


check button DNA-seq based exon junction arranged fusion gene breakpoints from dbVar. For the expressed sample information, go to Fusion Gene Sample section.
HgeneHchrHbpTgeneTchrTbpSV type
EML4chr242452626COX7A2Lchr242593850DEL
EML4chr242472642COX7A2Lchr242588306DEL
EML4chr242489246COX7A2Lchr242591350DUP
EML4chr242489247COX7A2Lchr242591348DUP
EML4chr242447941COX7A2Lchr242590394DUP
EML4chr242419829COX7A2Lchr242583667DEL
EML4chr242462880COX7A2Lchr242583667DEL


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Tumorigenic MoA (Mechanism of Action) Scenarios of Fusion Genes for EML4_COX7A2L


check button To generate these tumorigenic scenario annotations, we implemented a deduction-first, retrieval-later computational framework. The pipeline first applies rule-guided reasoning across ten core mechanistic categories (M1–M10) derived from fusion gene biology to infer candidate mechanisms, tumorigenic scenarios, targeting points, and targeting backgrounds. To ensure empirical accountability, a governed Python workflow retrieves literature candidates via NCBI E-utilities and Europe PMC using tiered searches. Using JSON Schema-constrained LLM evidence judges (GPT-5.6 Luna and Terra), retrieved articles are evaluated for specificity and confidence without de novo PMID generation. This produces two distinct versions: a strict version restricted to high- or medium-confidence fusion-specific evidence, and an extended version incorporating broader gene-, pathway-, and contextual evidence.
* We have 10 tumorigenic mechanism categories of fusion genes as shown below.
Constitutively Active Kinases, Catalytic Domain Dysregulation, & Transmembrane Ligand FusionsAberrant Chimeric Transcription Factor / Fusion Transcription Factor ActivityEpigenetic Reprogramming / Histone Modifier DysregulationChromatin Remodeling DysregulationCondensate-Driven Transcriptional Rewiring / LLPPromoter / Enhancer HijackingDominant-Negative AntagonismCell Cycle / Checkpoint Bypass / RNA Processing DysregulationSubcellular Mislocalization / Spatial DysregulationNuclear Body / Sub-organellar Architecture Disruption & Differentiation Blockade

* Strict version: Restricted to high- or medium-confidence fusion-specific evidence.
Fusion Gene NameMechanism CategoryMechanism PubMedTumorigenic ScenariosTumorigenic Scenario PubMedTargeting PointsTargeting PubMedMechanism BackgroundMechanism Background PubMed

* Extended version: Includes all strict-level fusion evidence plus broader gene-, pathway-, and low-confidence contextual evidence.
Fusion Gene NameMechanism CategoryMechanism PubMedTumorigenic ScenariosTumorigenic Scenario PubMedTargeting PointsTargeting PubMedMechanism BackgroundMechanism Background PubMed

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EML4

Q9HC35

.

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID

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Fusion Genomic Features for EML4_COX7A2L


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence) of In-frame fusion genes. FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
EML4chr242396776+COX7A2Lchr242580483-1.23e-061.00e+00
EML4chr242396776-COX7A2Lchr242580483-9.99e-011.02e-03


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence) of 5UTR-3CSD fusion genes (N-truncated cases).
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence) of 5CDS-3UTR fusion genes (C-truncated cases).
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of six genomic regulatory feature tracks across a ±5 kb window centered on the fusion breakpoints. We input the breakpoint sequences into AlphaGenome and obtained predicted genome tracks at single-base-pair resolution for each modality by running a single forward pass over the reference sequence. Specifically, for each breakpoint, AlphaGenome processed and returned predicted track data across diverse modalities, which were then averaged across all tracks within each output type and visualized across the ±5 kb window. The left panel shows the 5'-gene breakpoint ±5 kb area, and the right panel shows the 3'-gene breakpoint area, with tracks grouped by category: chromatin accessibility (DNase-seq, ATAC-seq), active transcription (RNA-seq, CAGE), and chromatin binding (ChIP-Histone, ChIP-TF).

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Fusion Gene ORF Annotations for EML4_COX7A2L

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
3UTR-3CDSENST00000482660ENST00000378669EML4chr2

42396776

-COX7A2Lchr2

42580483

-
3UTR-5UTRENST00000482660ENST00000234301EML4chr2

42396776

-COX7A2Lchr2

42580483

-
3UTR-5UTRENST00000482660ENST00000463055EML4chr2

42396776

-COX7A2Lchr2

42580483

-
3UTR-5UTRENST00000482660ENST00000482463EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000318522ENST00000234301EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000318522ENST00000463055EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000318522ENST00000482463EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000401738ENST00000234301EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000401738ENST00000463055EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000401738ENST00000482463EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000402711ENST00000234301EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000402711ENST00000463055EML4chr2

42396776

-COX7A2Lchr2

42580483

-
5CDS-5UTRENST00000402711ENST00000482463EML4chr2

42396776

-COX7A2Lchr2

42580483

-
Frame-shiftENST00000318522ENST00000378669EML4chr2

42396776

-COX7A2Lchr2

42580483

-
Frame-shiftENST00000401738ENST00000378669EML4chr2

42396776

-COX7A2Lchr2

42580483

-
Frame-shiftENST00000402711ENST00000378669EML4chr2

42396776

-COX7A2Lchr2

42580483

-

check buttonORFfinder Result Based On The Fusion Transcript Sequences of the In-frame Fusion Genes.
HenstTenstHgeneHchrHbpTgeneTchrTbpSeq length
(transcript)
Seq length
(peptide)

check buttonORFfinder Result Based On The Fusion Transcript Sequences of the 5UTR-3CDS Fusion Genes for N-Truncated Protein Search.
HenstTenstHgeneHchrHbpTgeneTchrTbpSeq length
(transcript)
Seq length
(peptide)

check buttonORFfinder Result Based On The Fusion Transcript Sequences of the 5CDS-3UTR Fusion Genes for C-Truncated Protein Search.
HenstTenstHgeneHchrHbpTgeneTchrTbpSeq length
(transcript)
Seq length
(peptide)

check buttonDeepORF Prediction of The Coding Potential Based on The Fusion Transcript Sequence of In-frame Fusion Genes. DeepORF is a Coding Potential Classifier Based on Convolutional Neural Network by Comparing the Real Ribo-seq Data. If the No-coding Score < 0.5 and Coding Score > 0.5, Then The In-frame Fusion Transcript is Predicted as Being Likely Translated.
HenstTenstHgeneHchrHbpTgeneTchrTbpNo-coding scoreCoding score

check buttonDeepORF Prediction of The Coding Potential Based on The Fusion Transcript Sequence of 5UTR-3CDS Fusion Genes (Potential N-Truncated Proteins).
HenstTenstHgeneHchrHbpTgeneTchrTbpNo-coding scoreCoding score

check buttonDeepORF Prediction of The Coding Potential Based on The Fusion Transcript Sequence of 5CDS-3UTR Fusion Genes (Potential C-Truncated Proteins).
HenstTenstHgeneHchrHbpTgeneTchrTbpNo-coding scoreCoding score

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Fusion Protein Retained/Non-Retained Functional Features for EML4_COX7A2L

check buttonProtein Level Annotation from FGviewer
* Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at download page. Minus value of BPloci means that the break pointn is located before the CDS.
fgviewer annotation
- In-frame and retained protein feature among the 13 regional features (visualization across fusion protein length).
No matching images found for ${hg}_${tg}.

- In-frame and retained protein feature among the 13 regional features (texts).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


check button - Retained PPIs in in-frame fusion.
PartnerHgeneHbpTgeneTbpENSTUniProtStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerHgeneHbpTgeneTbpENSTUniProtStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Fusion Transcript Sequence for EML4_COX7A2L

check button In-frame Fusion Transcript Sequences.

check button N-Truncated Transcript (5UTR-3CDS) Sequences

check button C-Truncated Transcript (5CDS-3UTR) Sequences

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Fusion Protein Sequence for EML4_COX7A2L

check button In-frame Fusion Protein Sequences.

check button N-Truncated Protein (5UTR-3CDS) Sequences

check button C-Truncated Protein (5CDS-3UTR) Sequences

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Personalized Fusion Protein Sequence for EML4_COX7A2L


check button TCGA Kinase/DNA-binding Domain Mutated Fusion Protein Sequences
NumGene GroupDomain LociFusion Protein IDFusion Gene NamePartnerMutated Residue in WT ProteinSeq. LengthMutated Residue in Fusion Protein

check button CCLE Kinase/DNA-binding Domain Mutated Fusion Protein Sequences

NumGene GroupDomain LociFusion Protein IDFusion Gene NamePartnerMutated Residue in WT ProteinSeq. LengthMutated Residue in Fusion Protein

check button TCGA All Mutated Fusion Protein Sequences


Fusion Protein IDSample IDMutated PartnerAAchange in WTSeq. LengthAAchange in Fusion

check button CCLE All Mutated Fusion Protein Sequences


Fusion Protein IDSample IDMutated PartnerAAchange in WTSeq. LengthAAchange in Fusion

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Fusion Gene Exprssed Samples for EML4_COX7A2L


check buttonRNA-seq based fusion gene expressed samples.
SourceStudyDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDBBRCATCGA-E9-A245-01AEML4

chr2

42396776-COX7A2L

chr2

42580483

-
ChimerDBBRCATCGA-E9-A245-01AEML4

chr2

42396776+COX7A2L

chr2

42580483

-
ChimerDBLUSCTCGA-77-8143-01AEML4

chr2

42531691-COX7A2L

chr2

42561009

-
ChimerDBLUSCTCGA-77-8143EML4

chr2

42396776+COX7A2L

chr2

42580483

-
ChimerDBLUSCTCGA-77-8143EML4

chr2

42531691+COX7A2L

chr2

42561009

-
TCGAfusionPortalBRCATCGA-E9-A245-01AEML4

chr2

42396776+COX7A2L

chr2

42580483

-

check buttonDNA-seq based fusion gene expressed samples.
SourceStudyDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrandSV type
dbVarnstd130Unknown_CellEML4

chr2

42452626COX7A2L

chr2

42593850

DEL
dbVarnstd151Unknown_CellEML4

chr2

42472642COX7A2L

chr2

42588306

DEL
dbVarnstd200Unknown_CellEML4

chr2

42489246COX7A2L

chr2

42591350

DUP
dbVarnstd223Unknown_CellEML4

chr2

42489247COX7A2L

chr2

42591348

DUP
dbVarnstd229Unknown_CellEML4

chr2

42447941COX7A2L

chr2

42590394

DUP
dbVarnstd239Unknown_CellWG1004324-DNAD02-010719-1047560511EML4

chr2

42419829COX7A2L

chr2

42583667

DEL
dbVarnstd239Unknown_CellWG1004369-DNAA06-014687-0095503770EML4

chr2

42462880COX7A2L

chr2

42583667

DEL


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Related Drugs for EML4_COX7A2L


check button PubMed Abstract Search With ['A-B' AND 'drug'], ['A::B' AND 'drug']
* For more details on the Studied, Reported, Approved Drugs targeting this fusion gene, Go to FusionPub.
PMIDFusion Gene NameDrugStudy Title

check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status