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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:RERE-CYP4A11

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RERE-CYP4A11
FusionPDB ID: 73492
FusionGDB2.0 ID: 73492
HgeneTgene
Gene symbol

RERE

CYP4A11

Gene ID

473

1579

Gene namearginine-glutamic acid dipeptide repeatscytochrome P450 family 4 subfamily A member 11
SynonymsARG|ARP|ATN1L|DNB1|NEDBEHCP4Y|CYP4A2|CYP4AII|CYPIVA11
Cytomap

1p36.23

1p33

Type of geneprotein-codingprotein-coding
Descriptionarginine-glutamic acid dipeptide repeats proteinarginine-glutamic acid dipeptide (RE) repeatsatrophin 2atrophin-1 like proteinatrophin-1 related proteincytochrome P450 4A1120-HETE synthase20-hydroxyeicosatetraenoic acid synthaseP450HL-omegaalkane-1 monooxygenasecytochrome P-450HK-omegacytochrome P450, family 4, subfamily A, polypeptide 11cytochrome P450, subfamily IVA, polypeptide 11cytochrome P4
Modification date2020031320200313
UniProtAcc.

Q02928

Main function of 5'-partner protein: FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of fatty acids and their oxygenated derivatives (oxylipins) (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:10553002, PubMed:10660572, PubMed:15611369). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase) (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:10553002, PubMed:10660572, PubMed:15611369). Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of saturated and unsaturated fatty acids, the catalytic efficiency decreasing in the following order: dodecanoic > tetradecanoic > (9Z)-octadecenoic > (9Z,12Z)-octadecadienoic > hexadecanoic acid (PubMed:10553002, PubMed:10660572). Acts as a major omega-hydroxylase for dodecanoic (lauric) acid in liver (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:15611369). Participates in omega-hydroxylation of (5Z,8Z,11Z,14Z)-eicosatetraenoic acid (arachidonate) to 20-hydroxyeicosatetraenoic acid (20-HETE), a signaling molecule acting both as vasoconstrictive and natriuretic with overall effect on arterial blood pressure (PubMed:10620324, PubMed:10660572, PubMed:15611369). Can also catalyze the oxidation of the penultimate carbon (omega-1 oxidation) of fatty acids with lower efficiency (PubMed:7679927). May contribute to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acid, thereby initiating chain shortening (PubMed:18182499). Omega-hydroxylates (9R,10S)-epoxy-octadecanoate stereoisomer (PubMed:15145985). Plays a minor role in omega-oxidation of long-chain 3-hydroxy fatty acids (PubMed:18065749). Has little activity toward prostaglandins A1 and E1 (PubMed:7679927). {ECO:0000269|PubMed:10553002, ECO:0000269|PubMed:10620324, ECO:0000269|PubMed:10660572, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15611369, ECO:0000269|PubMed:1739747, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:7679927, ECO:0000269|PubMed:8914854}.
Ensembl transtripts involved in fusion geneENST idsENST00000337907, ENST00000377464, 
ENST00000400907, ENST00000400908, 
ENST00000460659, ENST00000476556, 
ENST00000457840, ENST00000496519, 
ENST00000310638, ENST00000371904, 
ENST00000371905, ENST00000462347, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score27 X 28 X 11=83161 X 1 X 1=1
# samples 431
** MAII scorelog2(43/8316*10)=-4.27348119326891
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Fusion gene context

PubMed: RERE [Title/Abstract] AND CYP4A11 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: RERE [Title/Abstract] AND CYP4A11 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RERE(8525985)-CYP4A11(47403809), # samples:3
Anticipated loss of major functional domain due to fusion event.RERE-CYP4A11 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.
RERE-CYP4A11 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.
RERE-CYP4A11 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.
RERE-CYP4A11 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.
RERE-CYP4A11 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneCYP4A11

GO:0001676

long-chain fatty acid metabolic process

18433732

TgeneCYP4A11

GO:0006691

leukotriene metabolic process

9799565

TgeneCYP4A11

GO:0019369

arachidonic acid metabolic process

10660572

TgeneCYP4A11

GO:0019373

epoxygenase P450 pathway

9618440

TgeneCYP4A11

GO:0055114

oxidation-reduction process

9618440|9799565|18433732



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/chr1:8525985/chr1:47403809)
- 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 RERE (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 CYP4A11 (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)
ENST00000337907REREchr18525985-ENST00000310638CYP4A11chr147403809-414118385333202889
ENST00000337907REREchr18525985-ENST00000371904CYP4A11chr147403809-338018385333205890
ENST00000337907REREchr18525985-ENST00000462347CYP4A11chr147403809-338718385332908791
ENST00000337907REREchr18525985-ENST00000371905CYP4A11chr147403809-333718385333010825
ENST00000377464REREchr18525985-ENST00000310638CYP4A11chr147403809-28575541551918587
ENST00000377464REREchr18525985-ENST00000371904CYP4A11chr147403809-20965541551921588
ENST00000377464REREchr18525985-ENST00000462347CYP4A11chr147403809-21035541551624489
ENST00000377464REREchr18525985-ENST00000371905CYP4A11chr147403809-20535541551726523
ENST00000400907REREchr18525985-ENST00000310638CYP4A11chr147403809-35801277742641855
ENST00000400907REREchr18525985-ENST00000371904CYP4A11chr147403809-28191277742644856
ENST00000400907REREchr18525985-ENST00000462347CYP4A11chr147403809-28261277742347757
ENST00000400907REREchr18525985-ENST00000371905CYP4A11chr147403809-27761277742449791

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
ENST00000337907ENST00000310638REREchr18525985-CYP4A11chr147403809-0.0014173780.9985826
ENST00000337907ENST00000371904REREchr18525985-CYP4A11chr147403809-0.0023465610.9976534
ENST00000337907ENST00000462347REREchr18525985-CYP4A11chr147403809-0.0030027010.99699736
ENST00000337907ENST00000371905REREchr18525985-CYP4A11chr147403809-0.0019880690.99801195
ENST00000377464ENST00000310638REREchr18525985-CYP4A11chr147403809-0.0107788050.9892212
ENST00000377464ENST00000371904REREchr18525985-CYP4A11chr147403809-0.0123648910.9876351
ENST00000377464ENST00000462347REREchr18525985-CYP4A11chr147403809-0.0335939640.966406
ENST00000377464ENST00000371905REREchr18525985-CYP4A11chr147403809-0.0116822470.9883178
ENST00000400907ENST00000310638REREchr18525985-CYP4A11chr147403809-0.0016106110.99838936
ENST00000400907ENST00000371904REREchr18525985-CYP4A11chr147403809-0.002807920.9971921
ENST00000400907ENST00000462347REREchr18525985-CYP4A11chr147403809-0.003559190.9964408
ENST00000400907ENST00000371905REREchr18525985-CYP4A11chr147403809-0.0023341310.9976659

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 RERE-CYP4A11

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
REREchr18525985CYP4A11chr1474038091277401PKLIEKCWTEDEVLQQDQELQRIQKW
REREchr18525985CYP4A11chr1474038091277463KSHGSYRFLAPWIGYGLLLLNGQTWF
REREchr18525985CYP4A11chr1474038091277692QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr1474038091277790QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr1474038091277791QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr1474038091838435PKLIEKCWTEDEVLQQDQELQRIQKW
REREchr18525985CYP4A11chr1474038091838497KSHGSYRFLAPWIGYGLLLLNGQTWF
REREchr18525985CYP4A11chr1474038091838726QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr1474038091838824QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr1474038091838825QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr147403809554133PKLIEKCWTEDEVLQQDQELQRIQKW
REREchr18525985CYP4A11chr147403809554195KSHGSYRFLAPWIGYGLLLLNGQTWF
REREchr18525985CYP4A11chr147403809554424QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr147403809554522QHSHAFLPFSGGSRNCIGKQFAMNEL
REREchr18525985CYP4A11chr147403809554523QHSHAFLPFSGGSRNCIGKQFAMNEL

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Potential FusionNeoAntigen Information of RERE-CYP4A11 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.
RERE-CYP4A11_8525985_47403809.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)
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:05SRNCIGKQF0.99860.66241221
RERE-CYP4A11chr18525985chr1474038091838HLA-A31:02AFLPFSGGSR0.97270.8615414
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:05SRNCIGKQFAM10.68061223
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:04SRNCIGKQFAM10.52611223
RERE-CYP4A11chr18525985chr1474038091838HLA-A68:24HAFLPFSGGSR0.99850.5883314
RERE-CYP4A11chr18525985chr1474038091838HLA-A68:03HAFLPFSGGSR0.99780.5745314
RERE-CYP4A11chr18525985chr1474038091838HLA-A68:05HAFLPFSGGSR0.99650.5886314
RERE-CYP4A11chr18525985chr1474038091838HLA-A33:05HAFLPFSGGSR0.9960.502314
RERE-CYP4A11chr18525985chr1474038091838HLA-A33:01HAFLPFSGGSR0.9960.502314
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:14SRNCIGKQF0.99830.55841221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:95SRNCIGKQF0.99650.52671221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:05SRNCIGKQF0.99580.85851221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:27SRNCIGKQF0.98840.8671221
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:03SRNCIGKQF0.97250.68681221
RERE-CYP4A11chr18525985chr1474038091838HLA-B39:12SRNCIGKQF0.8210.8551221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:19SRNCIGKQF0.80290.57061221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:10SRNCIGKQF0.80050.88041221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:67SRNCIGKQF0.79970.89151221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:80SRNCIGKQF0.79970.89151221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:46SRNCIGKQF0.79870.74981221
RERE-CYP4A11chr18525985chr1474038091838HLA-C12:16SRNCIGKQF0.04850.90991221
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:03SRNCIGKQFAM0.99960.69691223
RERE-CYP4A11chr18525985chr1474038091838HLA-A68:01HAFLPFSGGSR0.99850.5883314
RERE-CYP4A11chr18525985chr1474038091838HLA-A33:03HAFLPFSGGSR0.99340.5429314
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:10SRNCIGKQF0.99850.66041221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:01SRNCIGKQF0.99640.51661221
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:09SRNCIGKQF0.99050.55091221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:17SRNCIGKQF0.9350.92441221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:02SRNCIGKQF0.79970.89151221
RERE-CYP4A11chr18525985chr1474038091838HLA-C07:22SRNCIGKQF0.7970.50541221
RERE-CYP4A11chr18525985chr1474038091838HLA-C06:08SRNCIGKQF0.76820.96451221
RERE-CYP4A11chr18525985chr1474038091838HLA-C06:06SRNCIGKQF0.22110.98241221
RERE-CYP4A11chr18525985chr1474038091838HLA-C06:17SRNCIGKQF0.03480.98461221
RERE-CYP4A11chr18525985chr1474038091838HLA-C06:02SRNCIGKQF0.03480.98461221
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:10SRNCIGKQFAM10.69151223
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:06SRNCIGKQFAM10.50171223
RERE-CYP4A11chr18525985chr1474038091838HLA-B27:09SRNCIGKQFAM0.99990.57241223

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Potential FusionNeoAntigen Information of RERE-CYP4A11 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.
RERE-CYP4A11_8525985_47403809.msa

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)
RERE-CYP4A11chr18525985chr1474038091838DRB5-0103QHSHAFLPFSGGSRN015
RERE-CYP4A11chr18525985chr1474038091838DRB5-0103HSHAFLPFSGGSRNC116
RERE-CYP4A11chr18525985chr1474038091838DRB5-0103SHAFLPFSGGSRNCI217
RERE-CYP4A11chr18525985chr1474038091838DRB5-0111QHSHAFLPFSGGSRN015
RERE-CYP4A11chr18525985chr1474038091838DRB5-0203QHSHAFLPFSGGSRN015
RERE-CYP4A11chr18525985chr1474038091838DRB5-0203HSHAFLPFSGGSRNC116
RERE-CYP4A11chr18525985chr1474038091838DRB5-0203SHAFLPFSGGSRNCI217

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Fusion breakpoint peptide structures of RERE-CYP4A11

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
5382LPFSGGSRNCIGKQRERECYP4A11chr18525985chr1474038091838

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of RERE-CYP4A11

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-B14:023BVN5382LPFSGGSRNCIGKQ-8.31227-8.42567
HLA-B14:023BVN5382LPFSGGSRNCIGKQ-5.57336-6.60866
HLA-B52:013W395382LPFSGGSRNCIGKQ-6.32748-6.44088
HLA-B52:013W395382LPFSGGSRNCIGKQ-5.21657-6.25187
HLA-A24:025HGA5382LPFSGGSRNCIGKQ-6.95203-7.06543
HLA-A24:025HGA5382LPFSGGSRNCIGKQ-5.804-6.8393
HLA-B44:053DX85382LPFSGGSRNCIGKQ-6.02771-6.14111
HLA-B44:053DX85382LPFSGGSRNCIGKQ-3.1424-4.1777

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Vaccine Design for the FusionNeoAntigens of RERE-CYP4A11

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
RERE-CYP4A11chr18525985chr1474038091221SRNCIGKQFGTGCTCCAACAGGACCAGGAGCTACAA
RERE-CYP4A11chr18525985chr1474038091223SRNCIGKQFAMGTGCTCCAACAGGACCAGGAGCTACAACGGATT
RERE-CYP4A11chr18525985chr147403809314HAFLPFSGGSRATCGAGAAGTGCTGGACCGAGGACGAAGTGCTC
RERE-CYP4A11chr18525985chr147403809414AFLPFSGGSRGAGAAGTGCTGGACCGAGGACGAAGTGCTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
RERE-CYP4A11chr18525985chr147403809015QHSHAFLPFSGGSRNCCCAAGCTCATCGAGAAGTGCTGGACCGAGGACGAAGTGCTCCAA
RERE-CYP4A11chr18525985chr147403809116HSHAFLPFSGGSRNCAAGCTCATCGAGAAGTGCTGGACCGAGGACGAAGTGCTCCAACAG
RERE-CYP4A11chr18525985chr147403809217SHAFLPFSGGSRNCICTCATCGAGAAGTGCTGGACCGAGGACGAAGTGCTCCAACAGGAC

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Information of the samples that have these potential fusion neoantigens of RERE-CYP4A11

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
BRCARERE-CYP4A11chr18525985ENST00000337907chr147403809ENST00000310638TCGA-D8-A1XZ-01A

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Potential target of CAR-T therapy development for RERE-CYP4A11

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 RERE-CYP4A11

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 RERE-CYP4A11

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