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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:GLG1-BCAR1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GLG1-BCAR1
FusionPDB ID: 33240
FusionGDB2.0 ID: 33240
HgeneTgene
Gene symbol

GLG1

BCAR1

Gene ID

2734

9564

Gene namegolgi glycoprotein 1BCAR1 scaffold protein, Cas family member
SynonymsCFR-1|ESL-1|MG-160|MG160CAS|CAS1|CASS1|CRKAS|P130Cas
Cytomap

16q23.1

16q23.1

Type of geneprotein-codingprotein-coding
DescriptionGolgi apparatus protein 1E-selectin ligand 1cysteine-rich fibroblast growth factor receptorgolgi sialoglycoprotein MG-160breast cancer anti-estrogen resistance protein 1BCAR1, Cas family scaffold proteinBCAR1, Cas family scaffolding proteinCas scaffolding protein family member 1Crk-associated substrate p130Cas
Modification date2020031320200327
UniProtAcc

Q92896

Main function of 5'-partner protein: FUNCTION: Binds fibroblast growth factor and E-selectin (cell-adhesion lectin on endothelial cells mediating the binding of neutrophils). {ECO:0000269|PubMed:8985126}.

P56945

Main function of 5'-partner protein: FUNCTION: Docking protein which plays a central coordinating role for tyrosine kinase-based signaling related to cell adhesion (PubMed:12832404, PubMed:12432078). Implicated in induction of cell migration and cell branching (PubMed:12432078, PubMed:12832404, PubMed:17038317). Involved in the BCAR3-mediated inhibition of TGFB signaling (By similarity). {ECO:0000250|UniProtKB:Q61140, ECO:0000269|PubMed:12432078, ECO:0000269|PubMed:12832404, ECO:0000269|PubMed:17038317}.
Ensembl transtripts involved in fusion geneENST idsENST00000205061, ENST00000422840, 
ENST00000447066, 
ENST00000546196, 
ENST00000393420, ENST00000393422, 
ENST00000418647, ENST00000420641, 
ENST00000535626, ENST00000538440, 
ENST00000542031, ENST00000566982, 
ENST00000162330, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score23 X 21 X 12=57966 X 4 X 4=96
# samples 296
** MAII scorelog2(29/5796*10)=-4.320932789542
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/96*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: GLG1 [Title/Abstract] AND BCAR1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: GLG1 [Title/Abstract] AND BCAR1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GLG1(74640555)-BCAR1(75276988), # samples:1
Anticipated loss of major functional domain due to fusion event.GLG1-BCAR1 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.
GLG1-BCAR1 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.
GLG1-BCAR1 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.
GLG1-BCAR1 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
TgeneBCAR1

GO:0007015

actin filament organization

16105984

TgeneBCAR1

GO:0007229

integrin-mediated signaling pathway

8649368

TgeneBCAR1

GO:0010595

positive regulation of endothelial cell migration

21245381

TgeneBCAR1

GO:0016477

cell migration

9425168

TgeneBCAR1

GO:0030335

positive regulation of cell migration

9472046

TgeneBCAR1

GO:0050851

antigen receptor-mediated signaling pathway

10587647

TgeneBCAR1

GO:0050853

B cell receptor signaling pathway

9020138

TgeneBCAR1

GO:0086100

endothelin receptor signaling pathway

19086031



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/chr16:74640555/chr16:75276988)
- 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 GLG1 (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 BCAR1 (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)
ENST00000205061GLG1chr1674640555-ENST00000162330BCAR1chr1675276988-35404582030581012
ENST00000422840GLG1chr1674640555-ENST00000162330BCAR1chr1675276988-3520438030381012
ENST00000447066GLG1chr1674640555-ENST00000162330BCAR1chr1675276988-35384561830561012

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
ENST00000205061ENST00000162330GLG1chr1674640555-BCAR1chr1675276988-0.0030762440.99692374
ENST00000422840ENST00000162330GLG1chr1674640555-BCAR1chr1675276988-0.0028620950.9971379
ENST00000447066ENST00000162330GLG1chr1674640555-BCAR1chr1675276988-0.0030492390.99695075

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 GLG1-BCAR1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
GLG1chr1674640555BCAR1chr1675276988438146NLAVLECLQDVRENVLAKALYDNVAE
GLG1chr1674640555BCAR1chr1675276988456146NLAVLECLQDVRENVLAKALYDNVAE
GLG1chr1674640555BCAR1chr1675276988458146NLAVLECLQDVRENVLAKALYDNVAE

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Potential FusionNeoAntigen Information of GLG1-BCAR1 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.
GLG1-BCAR1_74640555_75276988.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)
GLG1-BCAR1chr1674640555chr1675276988458HLA-B45:01RENVLAKA0.99930.82571119
GLG1-BCAR1chr1674640555chr1675276988458HLA-B41:01RENVLAKA0.98670.79991119
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:01RENVLAKA0.93020.58151119
GLG1-BCAR1chr1674640555chr1675276988458HLA-A02:22CLQDVRENV0.99610.6377615
GLG1-BCAR1chr1674640555chr1675276988458HLA-B48:01LQDVRENVL0.99320.5229716
GLG1-BCAR1chr1674640555chr1675276988458HLA-A02:11CLQDVRENV0.99050.7469615
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:24LQDVRENVL0.97970.5478716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B14:02LQDVRENVL0.97850.6788716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B14:01LQDVRENVL0.97850.6788716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:03RENVLAKAL0.96930.92691120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:01LQDVRENVL0.90360.9367716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B45:01RENVLAKAL0.89780.75771120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:13RENVLAKAL0.80640.90471120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:13LQDVRENVL0.75660.967716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:37LQDVRENVL0.73010.7545716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:10LQDVRENVL0.71610.7734716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B38:01LQDVRENVL0.70440.9716716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B13:01LQDVRENVL0.59060.9884716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B41:01RENVLAKAL0.45170.8631120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:01RENVLAKAL0.34020.55251120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:03RENVLAKALY0.99960.93491121
GLG1-BCAR1chr1674640555chr1675276988458HLA-B40:06RENVLAKA0.99990.55261119
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:07LQDVRENVL0.99990.8716716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:10LQDVRENVL0.99990.8755716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C05:09LQDVRENVL0.99990.9643716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:15LQDVRENVL0.99980.9784716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B40:06RENVLAKAL0.99930.53241120
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:04LQDVRENVL0.98960.9698716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:13LQDVRENVL0.98960.9698716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:06LQDVRENVL0.98870.903716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:14LQDVRENVL0.97550.9015716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B73:01VRENVLAKA0.97480.70371019
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:03LQDVRENVL0.95350.9917716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B14:03LQDVRENVL0.92990.7384716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:08LQDVRENVL0.92220.9081716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:09LQDVRENVL0.92020.7697716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:12LQDVRENVL0.89560.9404716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:08RENVLAKAL0.8050.79341120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:05LQDVRENVL0.7130.9329716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:04RENVLAKA0.93020.58151119
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:05RENVLAKA0.93020.58151119
GLG1-BCAR1chr1674640555chr1675276988458HLA-C05:01LQDVRENVL0.99990.9643716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C01:03LQDVRENVL0.99990.953716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:01LQDVRENVL0.99990.8716716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C04:03LQDVRENVL0.99990.885716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:02LQDVRENVL0.99980.9784716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C18:01LQDVRENVL0.99980.881716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B40:04RENVLAKAL0.99910.52281120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:07RENVLAKAL0.96930.92691120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:13RENVLAKAL0.96930.92691120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:26RENVLAKAL0.96930.92691120
GLG1-BCAR1chr1674640555chr1675276988458HLA-C07:04LQDVRENVL0.96390.9352716
GLG1-BCAR1chr1674640555chr1675276988458HLA-C08:01LQDVRENVL0.95350.9917716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:31LQDVRENVL0.9250.9368716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:02LQDVRENVL0.91320.9647716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:11LQDVRENVL0.86460.8464716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B39:02RENVLAKAL0.80990.9051120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B18:11RENVLAKAL0.78410.77181120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B08:12LQDVRENVL0.76230.714716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B38:05LQDVRENVL0.70440.9716716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B18:03RENVLAKAL0.62020.72011120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:73LQDVRENVL0.56170.8538716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:09LQDVRENVL0.54120.7809716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B48:02RENVLAKAL0.43110.80461120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:30LQDVRENVL0.41930.9285716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B07:13LQDVRENVL0.41370.8138716
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:04RENVLAKAL0.34020.55251120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B50:05RENVLAKAL0.34020.55251120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:53RENVLAKAL0.12640.73461120
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:07RENVLAKALY0.99960.93491121
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:13RENVLAKALY0.99960.93491121
GLG1-BCAR1chr1674640555chr1675276988458HLA-B44:26RENVLAKALY0.99960.93491121
GLG1-BCAR1chr1674640555chr1675276988458HLA-B15:53RENVLAKALY0.95870.75351121
GLG1-BCAR1chr1674640555chr1675276988458HLA-A30:01QDVRENVLAK0.54630.7412818

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Potential FusionNeoAntigen Information of GLG1-BCAR1 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 GLG1-BCAR1

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
871CLQDVRENVLAKALGLG1BCAR1chr1674640555chr1675276988458

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of GLG1-BCAR1

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-B14:023BVN871CLQDVRENVLAKAL-7.15543-7.26883
HLA-B14:023BVN871CLQDVRENVLAKAL-4.77435-5.80965
HLA-B52:013W39871CLQDVRENVLAKAL-6.80875-6.92215
HLA-B52:013W39871CLQDVRENVLAKAL-4.20386-5.23916
HLA-A11:014UQ2871CLQDVRENVLAKAL-7.5194-8.5547
HLA-A11:014UQ2871CLQDVRENVLAKAL-6.9601-7.0735
HLA-A24:025HGA871CLQDVRENVLAKAL-7.52403-7.63743
HLA-A24:025HGA871CLQDVRENVLAKAL-5.82433-6.85963
HLA-B27:056PYJ871CLQDVRENVLAKAL-3.28285-4.31815
HLA-B44:053DX8871CLQDVRENVLAKAL-5.91172-6.94702
HLA-B44:053DX8871CLQDVRENVLAKAL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of GLG1-BCAR1

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
GLG1-BCAR1chr1674640555chr16752769881019VRENVLAKAGTGAGGGAGAACGTGCTGGCCAAAGCG
GLG1-BCAR1chr1674640555chr16752769881119RENVLAKAAGGGAGAACGTGCTGGCCAAAGCG
GLG1-BCAR1chr1674640555chr16752769881120RENVLAKALAGGGAGAACGTGCTGGCCAAAGCGCTC
GLG1-BCAR1chr1674640555chr16752769881121RENVLAKALYAGGGAGAACGTGCTGGCCAAAGCGCTCTAT
GLG1-BCAR1chr1674640555chr1675276988615CLQDVRENVTGCCTGCAGGATGTGAGGGAGAACGTG
GLG1-BCAR1chr1674640555chr1675276988716LQDVRENVLCTGCAGGATGTGAGGGAGAACGTGCTG
GLG1-BCAR1chr1674640555chr1675276988818QDVRENVLAKCAGGATGTGAGGGAGAACGTGCTGGCCAAA

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 GLG1-BCAR1

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
PRADGLG1-BCAR1chr1674640555ENST00000205061chr1675276988ENST00000162330TCGA-YJ-A8SW-01A

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Potential target of CAR-T therapy development for GLG1-BCAR1

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 GLG1-BCAR1

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 GLG1-BCAR1

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