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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:DTNB-ASXL2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DTNB-ASXL2
FusionPDB ID: 24368
FusionGDB2.0 ID: 24368
HgeneTgene
Gene symbol

DTNB

ASXL2

Gene ID

1838

55252

Gene namedystrobrevin betaASXL transcriptional regulator 2
Synonyms-ASXH2|SHAPNS
Cytomap

2p23.3

2p23.3

Type of geneprotein-codingprotein-coding
Descriptiondystrobrevin betaDTN-Bbeta-dystrobrevinputative Polycomb group protein ASXL2additional sex combs like 2, transcriptional regulatoradditional sex combs-like protein 2polycomb group protein ASXH2
Modification date2020032720200313
UniProtAcc

Q96EV8

Q76L83

Ensembl transtripts involved in fusion geneENST idsENST00000288642, ENST00000404103, 
ENST00000405222, ENST00000406818, 
ENST00000407038, ENST00000407186, 
ENST00000407661, ENST00000496972, 
ENST00000545439, ENST00000472690, 
ENST00000272341, ENST00000404843, 
ENST00000497092, ENST00000336112, 
ENST00000435504, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 10 X 7=70011 X 14 X 8=1232
# samples 1216
** MAII scorelog2(12/700*10)=-2.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1232*10)=-2.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: DTNB [Title/Abstract] AND ASXL2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DTNB(25818955)-ASXL2(25991737), # samples:3
ASXL2(26022254)-DTNB(25819109), # samples:1
Anticipated loss of major functional domain due to fusion event.ASXL2-DTNB 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.
ASXL2-DTNB 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.
DTNB-ASXL2 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.
DTNB-ASXL2 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.
DTNB-ASXL2 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.
DTNB-ASXL2 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.
DTNB-ASXL2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
DTNB-ASXL2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
DTNB-ASXL2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
DTNB-ASXL2 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
ASXL2-DTNB seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
ASXL2-DTNB seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ASXL2-DTNB seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ASXL2-DTNB seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted 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
TgeneASXL2

GO:0035360

positive regulation of peroxisome proliferator activated receptor signaling pathway

21047783

TgeneASXL2

GO:0045600

positive regulation of fat cell differentiation

21047783

TgeneASXL2

GO:0045944

positive regulation of transcription by RNA polymerase II

21047783


check buttonFusion gene breakpoints across DTNB (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 ASXL2 (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
ChimerDB4BRCATCGA-BH-A18V-06ADTNBchr2

25818955

-ASXL2chr2

25973282

-
ChimerDB4ESCATCGA-L5-A8NE-01ADTNBchr2

25818955

-ASXL2chr2

25991737

-
ChimerDB4ESCATCGA-L5-A8NEDTNBchr2

25818955

-ASXL2chr2

25991737

-
ChimerDB4STADTCGA-BR-4357-01ADTNBchr2

25754342

-ASXL2chr2

25994409

-


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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)
ENST00000496972DTNBchr225818955-ENST00000435504ASXL2chr225991737-1281973930745421411
ENST00000496972DTNBchr225818955-ENST00000336112ASXL2chr225991737-888073930745421411

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
ENST00000496972ENST00000435504DTNBchr225818955-ASXL2chr225991737-0.0001968250.99980325
ENST00000496972ENST00000336112DTNBchr225818955-ASXL2chr225991737-0.000330440.99966955

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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

>24368_24368_1_DTNB-ASXL2_DTNB_chr2_25818955_ENST00000496972_ASXL2_chr2_25991737_ENST00000336112_length(amino acids)=1411AA_BP=144
MIEAFRDNGLNTLDHTTEISVSRLETVISSIYYQLNKRLPSTHQISVEQSISLLLNFMIAAYDSEGRGKLTVFSVKAMLATMCGGKMLDK
LRYVFSQMSDSNGLMIFSKFDQFLKEVLKLPTAVFEGPSFGYTEHSVRTCFPQQALKQQQQKKQQQQCRPSISISSNQHLSLKTVKAASD
SVPAKPATWEGKQSDGQTGSPQNSNSSFSSSVKVENTLLGLGKKSFQRSERLHTRQMKRTKCADIDVETPDSILVNTNLRALINKHTFSV
LPGDCQQRLLLLLPEVDRQVGPDGLMKLNGSALNNEFFTSAAQGWKERLSEGEFTPEMQVRIRQEIEKEKKVEPWKEQFFESYYGQSSGL
SLEDSKKLTASPSDPKVKKTPAEQPKSMPVSEASLIRIVPVVSQSECKEEALQMSSPGRKEECESQGEVQPNFSTSSEPLLSSALNTHEL
SSILPIKCPKDEDLLEQKPVTSAEQESEKNHLTTASNYNKSESQESLVTSPSKPKSPGVEKPIVKPTAGAGPQETNMKEPLATLVDQSPE
SLKRKSSLTQEEAPVSWEKRPRVTENRQHQQPFQVSPQPFLNRGDRIQVRKVPPLKIPVSRISPMPFHPSQVSPRARFPVSITSPNRTGA
RTLADIKAKAQLVKAQRAAAAAAAAAAAAASVGGTIPGPGPGGGQGPGEGGEGQTARGGSPGSDRVSETGKGPTLELAGTGSRGGTRELL
PCGPETQPQSETKTTPSQAQPHSVSGAQLQQTPPVPPTPAVSGACTSVPSPAHIEKLDNEKLNPTRATATVASVSHPQGPSSCRQEKAPS
PTGPALISGASPVHCAADGTVELKAGPSKNIPNPSASSKTDASVPVAVTPSPLTSLLTTATLEKLPVPQVSATTAPAGSAPPSSTLPAAS
SLKTPGTSLNMNGPTLRPTSSIPANNPLVTQLLQGKDVPMEQILPKPLTKVEMKTVPLTAKEERGMGALIATNTTENSTREEVNERQSHP
ATQQQLGKTLQSKQLPQVPRPLQLFSAKELRDSSIDTHQYHEGLSKATQDQILQTLIQRVRRQNLLSVVPPSQFNFAHSGFQLEDISTSQ
RFMLGFAGRRTSKPAMAGHYLLNISTYGRGSESFRRTHSVNPEDRFCLSSPTEALKMGYTDCKNATGESSSSKEDDTDEESTGDEQESVT
VKEEPQVSQSAGKGDTSSGPHSRETLSTSDCLASKNVKAEIPLNEQTTLSKENYLFTRGQTFDEKTLARDLIQAAQKQMAHAVRGKAIRS
SPELFSSTVLPLPADSPTHQPLLLPPLQTPKLYGSPTQIGPSYRGMINVSTSSDMDHNSAVPGSQVSSNVGDVMSFSVTVTTIPASQAMN

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

>24368_24368_2_DTNB-ASXL2_DTNB_chr2_25818955_ENST00000496972_ASXL2_chr2_25991737_ENST00000435504_length(amino acids)=1411AA_BP=144
MIEAFRDNGLNTLDHTTEISVSRLETVISSIYYQLNKRLPSTHQISVEQSISLLLNFMIAAYDSEGRGKLTVFSVKAMLATMCGGKMLDK
LRYVFSQMSDSNGLMIFSKFDQFLKEVLKLPTAVFEGPSFGYTEHSVRTCFPQQALKQQQQKKQQQQCRPSISISSNQHLSLKTVKAASD
SVPAKPATWEGKQSDGQTGSPQNSNSSFSSSVKVENTLLGLGKKSFQRSERLHTRQMKRTKCADIDVETPDSILVNTNLRALINKHTFSV
LPGDCQQRLLLLLPEVDRQVGPDGLMKLNGSALNNEFFTSAAQGWKERLSEGEFTPEMQVRIRQEIEKEKKVEPWKEQFFESYYGQSSGL
SLEDSKKLTASPSDPKVKKTPAEQPKSMPVSEASLIRIVPVVSQSECKEEALQMSSPGRKEECESQGEVQPNFSTSSEPLLSSALNTHEL
SSILPIKCPKDEDLLEQKPVTSAEQESEKNHLTTASNYNKSESQESLVTSPSKPKSPGVEKPIVKPTAGAGPQETNMKEPLATLVDQSPE
SLKRKSSLTQEEAPVSWEKRPRVTENRQHQQPFQVSPQPFLNRGDRIQVRKVPPLKIPVSRISPMPFHPSQVSPRARFPVSITSPNRTGA
RTLADIKAKAQLVKAQRAAAAAAAAAAAAASVGGTIPGPGPGGGQGPGEGGEGQTARGGSPGSDRVSETGKGPTLELAGTGSRGGTRELL
PCGPETQPQSETKTTPSQAQPHSVSGAQLQQTPPVPPTPAVSGACTSVPSPAHIEKLDNEKLNPTRATATVASVSHPQGPSSCRQEKAPS
PTGPALISGASPVHCAADGTVELKAGPSKNIPNPSASSKTDASVPVAVTPSPLTSLLTTATLEKLPVPQVSATTAPAGSAPPSSTLPAAS
SLKTPGTSLNMNGPTLRPTSSIPANNPLVTQLLQGKDVPMEQILPKPLTKVEMKTVPLTAKEERGMGALIATNTTENSTREEVNERQSHP
ATQQQLGKTLQSKQLPQVPRPLQLFSAKELRDSSIDTHQYHEGLSKATQDQILQTLIQRVRRQNLLSVVPPSQFNFAHSGFQLEDISTSQ
RFMLGFAGRRTSKPAMAGHYLLNISTYGRGSESFRRTHSVNPEDRFCLSSPTEALKMGYTDCKNATGESSSSKEDDTDEESTGDEQESVT
VKEEPQVSQSAGKGDTSSGPHSRETLSTSDCLASKNVKAEIPLNEQTTLSKENYLFTRGQTFDEKTLARDLIQAAQKQMAHAVRGKAIRS
SPELFSSTVLPLPADSPTHQPLLLPPLQTPKLYGSPTQIGPSYRGMINVSTSSDMDHNSAVPGSQVSSNVGDVMSFSVTVTTIPASQAMN

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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/chr2:25818955/chr2:25991737)
- 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
DTNB

Q96EV8

ASXL2

Q76L83

FUNCTION: Component of the BLOC-1 complex, a complex that is required for normal biogenesis of lysosome-related organelles (LRO), such as platelet dense granules and melanosomes. In concert with the AP-3 complex, the BLOC-1 complex is required to target membrane protein cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals. The BLOC-1 complex, in association with SNARE proteins, is also proposed to be involved in neurite extension. Associates with the BLOC-2 complex to facilitate the transport of TYRP1 independent of AP-3 function. Plays a role in synaptic vesicle trafficking and in neurotransmitter release. Plays a role in the regulation of cell surface exposure of DRD2. May play a role in actin cytoskeleton reorganization and neurite outgrowth. May modulate MAPK8 phosphorylation. Appears to promote neuronal transmission and viability through regulating the expression of SNAP25 and SYN1, modulating PI3-kinase-Akt signaling and influencing glutamatergic release. Regulates the expression of SYN1 through binding to its promoter. Modulates prefrontal cortical activity via the dopamine/D2 pathway. {ECO:0000269|PubMed:15345706, ECO:0000269|PubMed:16837549, ECO:0000269|PubMed:17182842, ECO:0000269|PubMed:17989303, ECO:0000269|PubMed:19094965, ECO:0000269|PubMed:20180862, ECO:0000269|PubMed:20921223}.FUNCTION: Putative Polycomb group (PcG) protein. PcG proteins act by forming multiprotein complexes, which are required to maintain the transcriptionally repressive state of homeotic genes throughout development. PcG proteins are not required to initiate repression, but to maintain it during later stages of development. They probably act via methylation of histones, rendering chromatin heritably changed in its expressibility (By similarity). Involved in transcriptional regulation mediated by ligand-bound nuclear hormone receptors, such as peroxisome proliferator-activated receptor gamma (PPARG). Acts as coactivator for PPARG and enhances its adipocyte differentiation-inducing activity; the function seems to involve differential recruitment of acetylated and methylated histone H3. {ECO:0000250, ECO:0000269|PubMed:21047783}.

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
TgeneASXL2chr2:25818955chr2:25991737ENST000002723414131173_11760919.0Compositional biasNote=Poly-Ser
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413303_3070919.0Compositional biasNote=Poly-Leu
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413654_6840919.0Compositional biasNote=Ala-rich
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413687_7390919.0Compositional biasNote=Gly-rich
TgeneASXL2chr2:25818955chr2:25991737ENST0000027234141395_2350919.0Compositional biasNote=Ser-rich
TgeneASXL2chr2:25818955chr2:25991737ENST000004048431101173_11760919.0Compositional biasNote=Poly-Ser
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110303_3070919.0Compositional biasNote=Poly-Leu
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110654_6840919.0Compositional biasNote=Ala-rich
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110687_7390919.0Compositional biasNote=Gly-rich
TgeneASXL2chr2:25818955chr2:25991737ENST0000040484311095_2350919.0Compositional biasNote=Ser-rich
TgeneASXL2chr2:25818955chr2:25991737ENST000004355045131173_1176168.01436.0Compositional biasNote=Poly-Ser
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513303_307168.01436.0Compositional biasNote=Poly-Leu
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513654_684168.01436.0Compositional biasNote=Ala-rich
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513687_739168.01436.0Compositional biasNote=Gly-rich
TgeneASXL2chr2:25818955chr2:25991737ENST0000027234141311_860919.0DomainHTH HARE-type
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413274_3830919.0DomainDEUBAD
TgeneASXL2chr2:25818955chr2:25991737ENST0000040484311011_860919.0DomainHTH HARE-type
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110274_3830919.0DomainDEUBAD
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513274_383168.01436.0DomainDEUBAD
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413174_1780919.0MotifNuclear localization signal
TgeneASXL2chr2:25818955chr2:25991737ENST00000272341413887_8910919.0MotifNote=LXXLL motif 2
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110174_1780919.0MotifNuclear localization signal
TgeneASXL2chr2:25818955chr2:25991737ENST00000404843110887_8910919.0MotifNote=LXXLL motif 2
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513174_178168.01436.0MotifNuclear localization signal
TgeneASXL2chr2:25818955chr2:25991737ENST00000435504513887_891168.01436.0MotifNote=LXXLL motif 2
TgeneASXL2chr2:25818955chr2:25991737ENST000002723414131397_14340919.0Zinc fingerNote=PHD-type%3B atypical
TgeneASXL2chr2:25818955chr2:25991737ENST000004048431101397_14340919.0Zinc fingerNote=PHD-type%3B atypical
TgeneASXL2chr2:25818955chr2:25991737ENST000004355045131397_1434168.01436.0Zinc fingerNote=PHD-type%3B atypical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneDTNBchr2:25818955chr2:25991737ENST00000404103-620428_529201.0607.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000405222-618428_529201.0570.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000406818-621428_529201.0637.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000407038-619428_529201.0577.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000407661-620428_529201.0619.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000496972-518428_529144.0581.3333333333334Coiled coilOntology_term=ECO:0000255
HgeneDTNBchr2:25818955chr2:25991737ENST00000404103-620399_448201.0607.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000405222-618399_448201.0570.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000406818-621399_448201.0637.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000407038-619399_448201.0577.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000407661-620399_448201.0619.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000496972-518399_448144.0581.3333333333334RegionNote=Syntrophin-binding region
HgeneDTNBchr2:25818955chr2:25991737ENST00000404103-620237_284201.0607.3333333333334Zinc fingerZZ-type
HgeneDTNBchr2:25818955chr2:25991737ENST00000405222-618237_284201.0570.3333333333334Zinc fingerZZ-type
HgeneDTNBchr2:25818955chr2:25991737ENST00000406818-621237_284201.0637.3333333333334Zinc fingerZZ-type
HgeneDTNBchr2:25818955chr2:25991737ENST00000407038-619237_284201.0577.3333333333334Zinc fingerZZ-type
HgeneDTNBchr2:25818955chr2:25991737ENST00000407661-620237_284201.0619.3333333333334Zinc fingerZZ-type
HgeneDTNBchr2:25818955chr2:25991737ENST00000496972-518237_284144.0581.3333333333334Zinc fingerZZ-type
TgeneASXL2chr2:25818955chr2:25991737ENST0000043550451395_235168.01436.0Compositional biasNote=Ser-rich
TgeneASXL2chr2:25818955chr2:25991737ENST0000043550451311_86168.01436.0DomainHTH HARE-type


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>2046_DTNB_25818955_ASXL2_25991737_ranked_0.pdbDTNB2581895525818955ENST00000336112ASXL2chr225991737-
MIEAFRDNGLNTLDHTTEISVSRLETVISSIYYQLNKRLPSTHQISVEQSISLLLNFMIAAYDSEGRGKLTVFSVKAMLATMCGGKMLDK
LRYVFSQMSDSNGLMIFSKFDQFLKEVLKLPTAVFEGPSFGYTEHSVRTCFPQQALKQQQQKKQQQQCRPSISISSNQHLSLKTVKAASD
SVPAKPATWEGKQSDGQTGSPQNSNSSFSSSVKVENTLLGLGKKSFQRSERLHTRQMKRTKCADIDVETPDSILVNTNLRALINKHTFSV
LPGDCQQRLLLLLPEVDRQVGPDGLMKLNGSALNNEFFTSAAQGWKERLSEGEFTPEMQVRIRQEIEKEKKVEPWKEQFFESYYGQSSGL
SLEDSKKLTASPSDPKVKKTPAEQPKSMPVSEASLIRIVPVVSQSECKEEALQMSSPGRKEECESQGEVQPNFSTSSEPLLSSALNTHEL
SSILPIKCPKDEDLLEQKPVTSAEQESEKNHLTTASNYNKSESQESLVTSPSKPKSPGVEKPIVKPTAGAGPQETNMKEPLATLVDQSPE
SLKRKSSLTQEEAPVSWEKRPRVTENRQHQQPFQVSPQPFLNRGDRIQVRKVPPLKIPVSRISPMPFHPSQVSPRARFPVSITSPNRTGA
RTLADIKAKAQLVKAQRAAAAAAAAAAAAASVGGTIPGPGPGGGQGPGEGGEGQTARGGSPGSDRVSETGKGPTLELAGTGSRGGTRELL
PCGPETQPQSETKTTPSQAQPHSVSGAQLQQTPPVPPTPAVSGACTSVPSPAHIEKLDNEKLNPTRATATVASVSHPQGPSSCRQEKAPS
PTGPALISGASPVHCAADGTVELKAGPSKNIPNPSASSKTDASVPVAVTPSPLTSLLTTATLEKLPVPQVSATTAPAGSAPPSSTLPAAS
SLKTPGTSLNMNGPTLRPTSSIPANNPLVTQLLQGKDVPMEQILPKPLTKVEMKTVPLTAKEERGMGALIATNTTENSTREEVNERQSHP
ATQQQLGKTLQSKQLPQVPRPLQLFSAKELRDSSIDTHQYHEGLSKATQDQILQTLIQRVRRQNLLSVVPPSQFNFAHSGFQLEDISTSQ
RFMLGFAGRRTSKPAMAGHYLLNISTYGRGSESFRRTHSVNPEDRFCLSSPTEALKMGYTDCKNATGESSSSKEDDTDEESTGDEQESVT
VKEEPQVSQSAGKGDTSSGPHSRETLSTSDCLASKNVKAEIPLNEQTTLSKENYLFTRGQTFDEKTLARDLIQAAQKQMAHAVRGKAIRS
SPELFSSTVLPLPADSPTHQPLLLPPLQTPKLYGSPTQIGPSYRGMINVSTSSDMDHNSAVPGSQVSSNVGDVMSFSVTVTTIPASQAMN
1411


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
DTNB_pLDDT.png
all structure
all structure
ASXL2_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
DTNB
ASXL2all structure


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 DTNB-ASXL2


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 DTNB-ASXL2


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
TgeneASXL2C0005684Malignant neoplasm of urinary bladder1CTD_human
TgeneASXL2C0005695Bladder Neoplasm1CTD_human
TgeneASXL2C0023467Leukemia, Myelocytic, Acute1CTD_human
TgeneASXL2C0026998Acute Myeloid Leukemia, M11CTD_human
TgeneASXL2C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
TgeneASXL2C4310672SHASHI-PENA SYNDROME1GENOMICS_ENGLAND