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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:ARMC7-CDR2L

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARMC7-CDR2L
FusionPDB ID: 6665
FusionGDB2.0 ID: 6665
HgeneTgene
Gene symbol

ARMC7

CDR2L

Gene ID

79637

30850

Gene namearmadillo repeat containing 7cerebellar degeneration related protein 2 like
Synonyms-HUMPPA
Cytomap

17q25.1

17q25.1

Type of geneprotein-codingprotein-coding
Descriptionarmadillo repeat-containing protein 7cerebellar degeneration-related protein 2-likeparaneoplastic 62 kDa antigenparaneoplastic antigen
Modification date2020032720200313
UniProtAcc

Q9H6L4

Main function of 5'-partner protein:

Q86X02

Main function of 5'-partner protein:
Ensembl transtripts involved in fusion geneENST idsENST00000245543, ENST00000582136, 
ENST00000584947, ENST00000579096, 
ENST00000581078, 
ENST00000337231, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 3 X 5=1357 X 4 X 6=168
# samples 98
** MAII scorelog2(9/135*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ARMC7 [Title/Abstract] AND CDR2L [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARMC7 [Title/Abstract] AND CDR2L [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARMC7(73106701)-CDR2L(72995599), # samples:3
Anticipated loss of major functional domain due to fusion event.
* 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


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/chr17:73106701/chr17:72995599)
- 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 ARMC7 (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 CDR2L (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)
ENST00000582136ARMC7chr1773106701+ENST00000337231CDR2Lchr1772995599+35915462571864535
ENST00000245543ARMC7chr1773106701+ENST00000337231CDR2Lchr1772995599+35825372481855535
ENST00000584947ARMC7chr1773106701+ENST00000337231CDR2Lchr1772995599+3388343541661535

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
ENST00000582136ENST00000337231ARMC7chr1773106701+CDR2Lchr1772995599+0.005398610.99460137
ENST00000245543ENST00000337231ARMC7chr1773106701+CDR2Lchr1772995599+0.005438140.99456185
ENST00000584947ENST00000337231ARMC7chr1773106701+CDR2Lchr1772995599+0.0058045680.9941954

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 ARMC7-CDR2L

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARMC7chr1773106701CDR2Lchr177299559934396LSEENETLVEFAIDLHLAAELGKTLL
ARMC7chr1773106701CDR2Lchr177299559953796LSEENETLVEFAIDLHLAAELGKTLL
ARMC7chr1773106701CDR2Lchr177299559954696LSEENETLVEFAIDLHLAAELGKTLL

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Potential FusionNeoAntigen Information of ARMC7-CDR2L 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.
ARMC7-CDR2L_73106701_72995599.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)
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B13:01VEFAIDLHL0.99290.8295817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:24TLVEFAIDL0.98870.6744615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:67TLVEFAIDL0.98870.6744615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:30TLVEFAIDL0.98870.6744615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:60TLVEFAIDL0.98840.6663615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B35:04FAIDLHLAA0.98370.95721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B35:02FAIDLHLAA0.98370.95721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:16TLVEFAIDL0.98240.6115615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:04TLVEFAIDL0.97960.6343615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:29TLVEFAIDL0.96520.6781615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:19TLVEFAIDL0.95110.5283615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B44:03VEFAIDLHL0.91620.959817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:01VEFAIDLHL0.91550.9536817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B47:01VEFAIDLHL0.8580.605817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B08:09FAIDLHLAA0.84330.70331019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B39:13VEFAIDLHL0.3850.9261817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B41:01VEFAIDLHL0.25790.8872817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:01VEFAIDLHL0.22220.603817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B52:01VEFAIDLHL0.05420.8429817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B45:01VEFAIDLHLA0.96540.7948818
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:01VEFAIDLHLA0.66440.5684818
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:02VEFAIDLHLAA0.99240.5324819
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:01VEFAIDLHLAA0.98760.6166819
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C12:04FAIDLHLAA0.9990.9931019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C06:03FAIDLHLAA0.99870.99391019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:19FAIDLHLAA0.99860.98731019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B40:06VEFAIDLHL0.99860.5694817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C12:12FAIDLHLAA0.99710.95861019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C08:04FAIDLHLAA0.99680.94331019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C08:13FAIDLHLAA0.99680.94331019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:08FAIDLHLAA0.99220.90121019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-A02:01TLVEFAIDL0.98870.6744615
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C08:03FAIDLHLAA0.98730.98211019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B35:12FAIDLHLAA0.98370.95721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B78:01FAIDLHLAA0.97760.59351019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B39:08VEFAIDLHL0.55720.8702817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B40:06VEFAIDLHLA0.99040.5039818
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:07FAIDLHLAAEL10.99121021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:08FAIDLHLAAEL10.92721021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:19FAIDLHLAAEL10.9921021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B40:06VEFAIDLHLAA0.99960.5194819
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B40:04VEFAIDLHL0.99850.697817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:05FAIDLHLAA0.99830.92241019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:06FAIDLHLAA0.99760.98661019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C12:03FAIDLHLAA0.99730.98451019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C16:04FAIDLHLAA0.99720.98611019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:04FAIDLHLAA0.99680.98461019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:03FAIDLHLAA0.99680.98461019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:02FAIDLHLAA0.99670.9721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C12:02FAIDLHLAA0.99010.97851019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C08:01FAIDLHLAA0.98730.98211019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B35:09FAIDLHLAA0.98370.95721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B78:02FAIDLHLAA0.96280.64721019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:08VEFAIDLHL0.93070.9018817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B44:13VEFAIDLHL0.91620.959817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B44:07VEFAIDLHL0.91620.959817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B44:26VEFAIDLHL0.91620.959817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:05VEFAIDLHL0.91550.9536817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:06VEFAIDLHL0.90190.96817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B35:24FAIDLHLAA0.7890.90171019
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:03VEFAIDLHL0.78870.9488817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B18:11VEFAIDLHL0.50180.9216817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B39:02VEFAIDLHL0.41440.9315817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B41:03VEFAIDLHL0.31690.6096817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:05VEFAIDLHL0.22220.603817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:04VEFAIDLHL0.22220.603817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B48:02VEFAIDLHL0.19930.9258817
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:05VEFAIDLHLA0.66440.5684818
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:04VEFAIDLHLA0.66440.5684818
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:04FAIDLHLAAEL10.98931021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:05FAIDLHLAAEL10.92731021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:17FAIDLHLAAEL10.97031021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:03FAIDLHLAAEL10.98931021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C03:06FAIDLHLAAEL0.99950.99021021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-C17:01FAIDLHLAAEL0.99850.93221021
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:04VEFAIDLHLAA0.98760.6166819
ARMC7-CDR2Lchr1773106701chr1772995599537HLA-B50:05VEFAIDLHLAA0.98760.6166819

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Potential FusionNeoAntigen Information of ARMC7-CDR2L 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 ARMC7-CDR2L

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
9499TLVEFAIDLHLAAEARMC7CDR2Lchr1773106701chr1772995599537

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARMC7-CDR2L

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-B52:013W399499TLVEFAIDLHLAAE-7.90165-7.90165
HLA-B44:053DX89499TLVEFAIDLHLAAE-5.81679-5.81679

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Vaccine Design for the FusionNeoAntigens of ARMC7-CDR2L

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
ARMC7-CDR2Lchr1773106701chr17729955991019FAIDLHLAATTGCTATTGACTTGCACCTAGCTGCGG
ARMC7-CDR2Lchr1773106701chr17729955991021FAIDLHLAAELTTGCTATTGACTTGCACCTAGCTGCGGAGCTGG
ARMC7-CDR2Lchr1773106701chr1772995599615TLVEFAIDLCCCTGGTGGAGTTTGCTATTGACTTGC
ARMC7-CDR2Lchr1773106701chr1772995599817VEFAIDLHLTGGAGTTTGCTATTGACTTGCACCTAG
ARMC7-CDR2Lchr1773106701chr1772995599818VEFAIDLHLATGGAGTTTGCTATTGACTTGCACCTAGCTG
ARMC7-CDR2Lchr1773106701chr1772995599819VEFAIDLHLAATGGAGTTTGCTATTGACTTGCACCTAGCTGCGG

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 ARMC7-CDR2L

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
STADARMC7-CDR2Lchr1773106701ENST00000245543chr1772995599ENST00000337231TCGA-R5-A7ZE-01B

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Potential target of CAR-T therapy development for ARMC7-CDR2L

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

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 ARMC7-CDR2L

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 ARMC7-CDR2L

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