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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:MLLT3-IZUMO3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MLLT3-IZUMO3
FusionPDB ID: 54291
FusionGDB2.0 ID: 54291
HgeneTgene
Gene symbol

MLLT3

IZUMO3

Gene ID

4300

100129669

Gene nameMLLT3 super elongation complex subunitIZUMO family member 3
SynonymsAF9|YEATS3C9orf134|bA20A20.1
Cytomap

9p21.3

9p21.3

Type of geneprotein-codingprotein-coding
Descriptionprotein AF-9ALL1-fused gene from chromosome 9 proteinKMT2A/MLLT3 fusionKMT2A/MLLT3 fusion proteinYEATS domain-containing protein 3myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog); translocated to, 3myeloid/lymphoid or mixed-lineage leuizumo sperm-egg fusion protein 3
Modification date2020032720200313
UniProtAcc

P42568

.
Ensembl transtripts involved in fusion geneENST idsENST00000355930, ENST00000475957, 
ENST00000380338, ENST00000429426, 
ENST00000380321, 
ENST00000543880, 
ENST00000604921, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 14 X 11=27721 X 1 X 1=1
# samples 251
** MAII scorelog2(25/2772*10)=-3.47092725747513
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: MLLT3 [Title/Abstract] AND IZUMO3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MLLT3(20620653)-IZUMO3(24545059), # samples:3
Anticipated loss of major functional domain due to fusion event.MLLT3-IZUMO3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MLLT3-IZUMO3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MLLT3-IZUMO3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
MLLT3-IZUMO3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneMLLT3

GO:0045893

positive regulation of transcription, DNA-templated

25417107|27105114

HgeneMLLT3

GO:0090090

negative regulation of canonical Wnt signaling pathway

19591803


check buttonFusion gene breakpoints across MLLT3 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across IZUMO3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4GBMTCGA-32-5222-01AMLLT3chr9

20620653

-IZUMO3chr9

24545059

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000380338MLLT3chr920620653-ENST00000543880IZUMO3chr924545059-1176480287898203
ENST00000380338MLLT3chr920620653-ENST00000604921IZUMO3chr924545059-895480287880197
ENST00000429426MLLT3chr920620653-ENST00000543880IZUMO3chr924545059-97828298700200
ENST00000429426MLLT3chr920620653-ENST00000604921IZUMO3chr924545059-69728298682194

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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000380338ENST00000543880MLLT3chr920620653-IZUMO3chr924545059-0.0073729590.9926271
ENST00000380338ENST00000604921MLLT3chr920620653-IZUMO3chr924545059-0.0099819310.99001807
ENST00000429426ENST00000543880MLLT3chr920620653-IZUMO3chr924545059-0.0021099940.99789006
ENST00000429426ENST00000604921MLLT3chr920620653-IZUMO3chr924545059-0.0038909360.99610907

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>54291_54291_1_MLLT3-IZUMO3_MLLT3_chr9_20620653_ENST00000380338_IZUMO3_chr9_24545059_ENST00000543880_length(amino acids)=203AA_BP=64
MASSCAVQVKLELGHRAQVRKKPTVEGFTHDWMVFVRGPEHSNIQHFVEKVVFHLHESFPRPKRGVFIYQGKLLDVCQNLESKLKELLKN
FSEIACSEDCIVVEGPILDCWTCLRMTNRCFKGEYCGDEDPRKAENREIALFLILLATAVILGSAVLLFHFCIFHRRKMKAIRRSLKEYV

--------------------------------------------------------------

>54291_54291_2_MLLT3-IZUMO3_MLLT3_chr9_20620653_ENST00000380338_IZUMO3_chr9_24545059_ENST00000604921_length(amino acids)=197AA_BP=64
MASSCAVQVKLELGHRAQVRKKPTVEGFTHDWMVFVRGPEHSNIQHFVEKVVFHLHESFPRPKRGVFIYQGKLLDVCQNLESKLKELLKN
FSEIVVVEGPILDCWTCLRMTNRCFKGEYCGDEDPRKAENREIALFLILLATAVILGSAVLLFHFCIFHRRKMKAIRRSLKEYVEKKLEE

--------------------------------------------------------------

>54291_54291_3_MLLT3-IZUMO3_MLLT3_chr9_20620653_ENST00000429426_IZUMO3_chr9_24545059_ENST00000543880_length(amino acids)=200AA_BP=61
MCAVQVKLELGHRAQVRKKPTVEGFTHDWMVFVRGPEHSNIQHFVEKVVFHLHESFPRPKRGVFIYQGKLLDVCQNLESKLKELLKNFSE
IACSEDCIVVEGPILDCWTCLRMTNRCFKGEYCGDEDPRKAENREIALFLILLATAVILGSAVLLFHFCIFHRRKMKAIRRSLKEYVEKK

--------------------------------------------------------------

>54291_54291_4_MLLT3-IZUMO3_MLLT3_chr9_20620653_ENST00000429426_IZUMO3_chr9_24545059_ENST00000604921_length(amino acids)=194AA_BP=61
MCAVQVKLELGHRAQVRKKPTVEGFTHDWMVFVRGPEHSNIQHFVEKVVFHLHESFPRPKRGVFIYQGKLLDVCQNLESKLKELLKNFSE
IVVVEGPILDCWTCLRMTNRCFKGEYCGDEDPRKAENREIALFLILLATAVILGSAVLLFHFCIFHRRKMKAIRRSLKEYVEKKLEELMG

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr9:20620653/chr9:24545059)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MLLT3

P42568

.
FUNCTION: Chromatin reader component of the super elongation complex (SEC), a complex required to increase the catalytic rate of RNA polymerase II transcription by suppressing transient pausing by the polymerase at multiple sites along the DNA (PubMed:20159561, PubMed:20471948, PubMed:25417107, PubMed:27105114, PubMed:27545619). Specifically recognizes and binds acylated histone H3, with a preference for histone H3 that is crotonylated (PubMed:25417107, PubMed:27105114, PubMed:27545619, PubMed:30374167, PubMed:30385749). Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors (PubMed:25417107, PubMed:27105114, PubMed:27545619). Recognizes and binds histone H3 crotonylated at 'Lys-9' (H3K9cr), and with slightly lower affinity histone H3 crotonylated at 'Lys-18' (H3K18cr) (PubMed:27105114). Also recognizes and binds histone H3 acetylated and butyrylated at 'Lys-9' (H3K9ac and H3K9bu, respectively), but with lower affinity than crotonylated histone H3 (PubMed:25417107, PubMed:27105114, PubMed:30385749). In the SEC complex, MLLT3 is required to recruit the complex to crotonylated histones (PubMed:27105114, PubMed:27545619). Recruitment of the SEC complex to crotonylated histones promotes recruitment of DOT1L on active chromatin to deposit histone H3 'Lys-79' methylation (H3K79me) (PubMed:25417107). Plays a key role in hematopoietic stem cell (HSC) maintenance by preserving, rather than confering, HSC stemness (PubMed:31776511). Acts by binding to the transcription start site of active genes in HSCs and sustaining level of H3K79me2, probably by recruiting DOT1L (PubMed:31776511). {ECO:0000269|PubMed:20159561, ECO:0000269|PubMed:20471948, ECO:0000269|PubMed:25417107, ECO:0000269|PubMed:27105114, ECO:0000269|PubMed:27545619, ECO:0000269|PubMed:30374167, ECO:0000269|PubMed:30385749, ECO:0000269|PubMed:31776511}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention 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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-21156_5864.33333333333333569.0RegionInhibitor XL-07i binding
TgeneIZUMO3chr9:20620653chr9:24545059ENST0000054388017196_239100.33333333333333240.0Topological domainCytoplasmic
TgeneIZUMO3chr9:20620653chr9:24545059ENST0000054388017175_195100.33333333333333240.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211149_19464.33333333333333569.0Compositional biasNote=Poly-Ser
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211383_39164.33333333333333569.0Compositional biasNote=Poly-Ser
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211466_46964.33333333333333569.0Compositional biasNote=Poly-Pro
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-2111_13864.33333333333333569.0DomainYEATS
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211295_30064.33333333333333569.0MotifNuclear localization signal
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211106_10864.33333333333333569.0RegionHistone H3K9cr binding
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-211106_10964.33333333333333569.0RegionInhibitor XL-07i binding
HgeneMLLT3chr9:20620653chr9:24545059ENST00000380338-21178_8064.33333333333333569.0RegionHistone H3K9cr binding
TgeneIZUMO3chr9:20620653chr9:24545059ENST000005438801721_174100.33333333333333240.0Topological domainExtracellular


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors
MLLT3APPBP2, MCM6, BCOR, RBM48, EEF1A1, PTN, LRIF1, DOT1L, SGK1, AFF4, AFF1, CDK9, AFF3, ACACA, SIRT1, CCNT1, NIPBL, EAF1, ELL3, PCGF1, MLLT1, EEF2, ELL, MLLT10, CCNT2, RNF2, KMT2A, CHD4, ELL2, PAF1, Cbx8, APP, CDK6, MED26, HSP90B1, EXOSC3, FAM9A, EDA, DENND2D, EPB41L3, XPO1, Aff1, Mllt1, H3F3A, PIP4K2A, EPB41L2, CAMKV, MLLT6, SNX24, BPIFB1, MDK, PES1, EPB41L5, ARRB2, ORF35, ALKBH4, LRRK2, HIST1H3A, KIAA1429, HHT1, DYRK1A, MIIP, VAX1, ZNF572, CCAR2, STH1, TULP3, COIL, FGF11, CT45A5, FGF12, RASA2, NDUFAF4, CREB3L3, SMOC1, SYT2, RNF151, PLCD4, CEP89, DAXX, EPB41L1, PLCD3, KCNE3, SULF2, SKP1,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
MLLT3all structure
IZUMO3


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to MLLT3-IZUMO3


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to MLLT3-IZUMO3


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMLLT3C0005586Bipolar Disorder1PSYGENET