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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ATP11B-NIT2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP11B-NIT2
FusionPDB ID: 7738
FusionGDB2.0 ID: 7738
HgeneTgene
Gene symbol

ATP11B

NIT2

Gene ID

23200

56954

Gene nameATPase phospholipid transporting 11B (putative)nitrilase family member 2
SynonymsATPIF|ATPIRHEL-S-8a
Cytomap

3q26.33

3q12.2

Type of geneprotein-codingprotein-coding
Descriptionprobable phospholipid-transporting ATPase IFATPase IRATPase, class VI, type 11BP4-ATPase flippase complex alpha subunit ATP11Btruncated ATPase 11B proteinomega-amidase NIT2Nit protein 2epididymis secretory sperm binding protein Li 8anitrilase homolog 2
Modification date2020031320200313
UniProtAcc

Q9Y2G3

Main function of 5'-partner protein: FUNCTION: Catalytic component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of aminophospholipids, phosphatidylserines (PS) and phosphatidylethanolamines (PE), from the outer to the inner leaflet of intracellular membranes (PubMed:30018401). May contribute to the maintenance of membrane lipid asymmetry in endosome compartment (PubMed:30018401). {ECO:0000269|PubMed:30018401}.

Q9NQR4

Main function of 5'-partner protein: FUNCTION: Has omega-amidase activity (PubMed:22674578, PubMed:19595734). The role of omega-amidase is to remove potentially toxic intermediates by converting 2-oxoglutaramate and 2-oxosuccinamate to biologically useful 2-oxoglutarate and oxaloacetate, respectively (PubMed:19595734). {ECO:0000269|PubMed:19595734, ECO:0000269|PubMed:22674578}.
Ensembl transtripts involved in fusion geneENST idsENST00000482794, ENST00000323116, 
ENST00000493826, 
ENST00000394140, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 15 X 10=30005 X 5 X 5=125
# samples 226
** MAII scorelog2(22/3000*10)=-3.76938707185858
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/125*10)=-1.05889368905357
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ATP11B [Title/Abstract] AND NIT2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATP11B [Title/Abstract] AND NIT2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP11B(182566345)-NIT2(100071247), # samples:1
Anticipated loss of major functional domain due to fusion event.ATP11B-NIT2 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.
ATP11B-NIT2 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.
ATP11B-NIT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ATP11B-NIT2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ATP11B-NIT2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ATP11B-NIT2 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneNIT2

GO:0006107

oxaloacetate metabolic process

22674578

TgeneNIT2

GO:0006528

asparagine metabolic process

22674578

TgeneNIT2

GO:0006541

glutamine metabolic process

22674578



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/chr3:182566345/chr3:100071247)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across ATP11B (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 NIT2 (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 Amino Acid Sequences


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)
ENST00000323116ATP11Bchr3182566345+ENST00000394140NIT2chr3100071247+295611112061357383

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
ENST00000323116ENST00000394140ATP11Bchr3182566345+NIT2chr3100071247+0.0005750150.99942505

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for ATP11B-NIT2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATP11Bchr3182566345NIT2chr31000712471111302YKSKSQKRSAVEKAVDNQVYVATASP

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Potential FusionNeoAntigen Information of ATP11B-NIT2 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ATP11B-NIT2_182566345_100071247.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ATP11B-NIT2chr3182566345chr31000712471111HLA-B27:07KRSAVEKAV0.99850.5884615
ATP11B-NIT2chr3182566345chr31000712471111HLA-B50:02VEKAVDNQV0.98910.67311019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B45:01VEKAVDNQV0.98670.80071019
ATP11B-NIT2chr3182566345chr31000712471111HLA-A02:21KAVDNQVYV0.97230.52211221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B41:01VEKAVDNQV0.5710.78111019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B50:01VEKAVDNQV0.50750.87071019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B44:03VEKAVDNQVY0.99250.72361020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:01VEKAVDNQVY0.90240.60671020
ATP11B-NIT2chr3182566345chr31000712471111HLA-C04:06KAVDNQVYV0.99930.91751221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:07KAVDNQVYV0.99930.97781221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C15:06KAVDNQVYV0.99930.90431221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C15:04KAVDNQVYV0.99930.90961221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B40:06VEKAVDNQV0.99860.82481019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B27:14KRSAVEKAV0.99840.714615
ATP11B-NIT2chr3182566345chr31000712471111HLA-C05:09KAVDNQVYV0.99810.94431221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:19KAVDNQVYV0.99210.98551221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:08KAVDNQVYV0.98970.92341221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C08:13KAVDNQVYV0.9530.97761221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C08:04KAVDNQVYV0.9530.97761221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C12:04KAVDNQVYV0.94110.98971221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:03KAVDNQVYV0.92490.99011221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C02:06KAVDNQVYV0.82770.95561221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C12:12KAVDNQVYV0.81710.92431221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C08:03KAVDNQVYV0.77480.97891221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:14KAVDNQVYV0.6790.98191221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:02KAVDNQVY0.98830.96341220
ATP11B-NIT2chr3182566345chr31000712471111HLA-C16:01KAVDNQVY0.89150.94571220
ATP11B-NIT2chr3182566345chr31000712471111HLA-C15:02KAVDNQVYV0.99960.86751221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C15:05KAVDNQVYV0.99950.88461221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C15:09KAVDNQVYV0.99930.90961221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C04:04KAVDNQVYV0.99880.91521221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B27:09KRSAVEKAV0.99840.6988615
ATP11B-NIT2chr3182566345chr31000712471111HLA-B27:06KRSAVEKAV0.99840.6732615
ATP11B-NIT2chr3182566345chr31000712471111HLA-C04:03KAVDNQVYV0.99810.87611221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C05:01KAVDNQVYV0.99810.94431221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C16:02KAVDNQVYV0.99430.98611221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:17KAVDNQVYV0.990.97451221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B40:04VEKAVDNQV0.98950.87431019
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:06KAVDNQVYV0.97960.99081221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:05KAVDNQVYV0.97780.92921221
ATP11B-NIT2chr3182566345chr31000712471111HLA-A02:06KAVDNQVYV0.97230.52211221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:04KAVDNQVYV0.96730.99061221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C03:03KAVDNQVYV0.96730.99061221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:06KAVDNQVYV0.94450.98631221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:08KRSAVEKAV0.90690.9883615
ATP11B-NIT2chr3182566345chr31000712471111HLA-C16:01KAVDNQVYV0.90650.96761221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C17:01KAVDNQVYV0.90530.97561221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C16:04KAVDNQVYV0.90310.96221221
ATP11B-NIT2chr3182566345chr31000712471111HLA-A69:01KAVDNQVYV0.87170.57721221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:17KAVDNQVYV0.81740.98951221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:02KAVDNQVYV0.81740.98951221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C12:03KAVDNQVYV0.80270.97261221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C08:01KAVDNQVYV0.77480.97891221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:08KAVDNQVYV0.71620.99021221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C02:10KAVDNQVYV0.67480.97441221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C02:02KAVDNQVYV0.67480.97441221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C07:04KAVDNQVYV0.66480.87121221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B35:20EKAVDNQVY0.65560.61961120
ATP11B-NIT2chr3182566345chr31000712471111HLA-B35:13KAVDNQVYV0.6010.8791221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C12:02KAVDNQVYV0.5680.9491221
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:04EKAVDNQVY0.52320.62761120
ATP11B-NIT2chr3182566345chr31000712471111HLA-B50:04VEKAVDNQV0.50750.87071019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B50:05VEKAVDNQV0.50750.87071019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B41:03VEKAVDNQV0.45630.54321019
ATP11B-NIT2chr3182566345chr31000712471111HLA-B48:02EKAVDNQVY0.44210.58541120
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:06EKAVDNQVY0.30410.5941120
ATP11B-NIT2chr3182566345chr31000712471111HLA-B07:13KAVDNQVYV0.10450.70631221
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:17KRSAVEKAV0.00850.9815615
ATP11B-NIT2chr3182566345chr31000712471111HLA-C06:02KRSAVEKAV0.00850.9815615
ATP11B-NIT2chr3182566345chr31000712471111HLA-B15:53VEKAVDNQVY0.99320.55991020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B44:26VEKAVDNQVY0.99250.72361020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B44:13VEKAVDNQVY0.99250.72361020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B44:07VEKAVDNQVY0.99250.72361020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B15:54VEKAVDNQVY0.98510.51311020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B15:12VEKAVDNQVY0.96520.72251020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:04VEKAVDNQVY0.9370.63271020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:05VEKAVDNQVY0.90240.60671020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:06VEKAVDNQVY0.89670.59391020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B48:02VEKAVDNQVY0.85040.58951020
ATP11B-NIT2chr3182566345chr31000712471111HLA-B18:03VEKAVDNQVY0.84830.58961020

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Potential FusionNeoAntigen Information of ATP11B-NIT2 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

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Fusion breakpoint peptide structures of ATP11B-NIT2

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
4579KRSAVEKAVDNQVYATP11BNIT2chr3182566345chr31000712471111

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATP11B-NIT2

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN4579KRSAVEKAVDNQVY-7.15543-7.26883
HLA-B14:023BVN4579KRSAVEKAVDNQVY-4.77435-5.80965
HLA-B52:013W394579KRSAVEKAVDNQVY-6.80875-6.92215
HLA-B52:013W394579KRSAVEKAVDNQVY-4.20386-5.23916
HLA-A11:014UQ24579KRSAVEKAVDNQVY-7.5194-8.5547
HLA-A11:014UQ24579KRSAVEKAVDNQVY-6.9601-7.0735
HLA-A24:025HGA4579KRSAVEKAVDNQVY-7.52403-7.63743
HLA-A24:025HGA4579KRSAVEKAVDNQVY-5.82433-6.85963
HLA-B27:056PYJ4579KRSAVEKAVDNQVY-3.28285-4.31815
HLA-B44:053DX84579KRSAVEKAVDNQVY-5.91172-6.94702
HLA-B44:053DX84579KRSAVEKAVDNQVY-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ATP11B-NIT2

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
ATP11B-NIT2chr3182566345chr31000712471019VEKAVDNQVAGTAGAAAAGGCTGTTGATAATCAGGT
ATP11B-NIT2chr3182566345chr31000712471020VEKAVDNQVYAGTAGAAAAGGCTGTTGATAATCAGGTGTA
ATP11B-NIT2chr3182566345chr31000712471120EKAVDNQVYAGAAAAGGCTGTTGATAATCAGGTGTA
ATP11B-NIT2chr3182566345chr31000712471220KAVDNQVYAAAGGCTGTTGATAATCAGGTGTA
ATP11B-NIT2chr3182566345chr31000712471221KAVDNQVYVAAAGGCTGTTGATAATCAGGTGTATGT
ATP11B-NIT2chr3182566345chr3100071247615KRSAVEKAVGAAACGATCTGCAGTAGAAAAGGCTGT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

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Information of the samples that have these potential fusion neoantigens of ATP11B-NIT2

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
LUSCATP11B-NIT2chr3182566345ENST00000323116chr3100071247ENST00000394140TCGA-60-2726

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Potential target of CAR-T therapy development for ATP11B-NIT2

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneATP11Bchr3:182566345chr3:100071247ENST00000323116+103056_772831178.0TransmembraneHelical
HgeneATP11Bchr3:182566345chr3:100071247ENST00000323116+103083_1042831178.0TransmembraneHelical

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to ATP11B-NIT2

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 ATP11B-NIT2

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