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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:CDK5RAP1-CDH4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CDK5RAP1-CDH4
FusionPDB ID: 15260
FusionGDB2.0 ID: 15260
HgeneTgene
Gene symbol

CDK5RAP1

CDH4

Gene ID

51654

1002

Gene nameCDK5 regulatory subunit associated protein 1cadherin 4
SynonymsC20orf34|C42|CGI-05|HSPC167CAD4|R-CAD|RCAD
Cytomap

20q11.21

20q13.33

Type of geneprotein-codingprotein-coding
DescriptionCDK5 regulatory subunit-associated protein 1CDK5 activator-binding protein C42cadherin-4R-cadherincadherin 4, type 1, R-cadherin (retinal)cadherin 4, type 1, preproproteinretinal cadherin
Modification date2020031320200313
UniProtAcc

Q96SZ6

Main function of 5'-partner protein: FUNCTION: Methylthiotransferase that catalyzes the conversion of N6-(dimethylallyl)adenosine (i(6)A) to 2-methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 (adjacent to the 3'-end of the anticodon) of four mitochondrial DNA-encoded tRNAs (Ser(UCN), Phe, Tyr and Trp) (PubMed:22422838, PubMed:25738458, PubMed:28981754). Essential for efficient and highly accurate protein translation by the ribosome (PubMed:22422838, PubMed:25738458, PubMed:28981754). Specifically inhibits CDK5 activation by CDK5R1 (PubMed:11882646). Essential for efficient mitochondrial protein synthesis and respiratory chain; shows pathological consequences in mitochondrial disease (PubMed:25738458). {ECO:0000269|PubMed:11882646, ECO:0000269|PubMed:22422838, ECO:0000269|PubMed:25738458, ECO:0000269|PubMed:28981754}.

P55283

Main function of 5'-partner protein: FUNCTION: Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. May play an important role in retinal development.
Ensembl transtripts involved in fusion geneENST idsENST00000477105, ENST00000473997, 
ENST00000346416, ENST00000357886, 
ENST00000544843, ENST00000339269, 
ENST00000360469, ENST00000543233, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 5=21016 X 14 X 7=1568
# samples 721
** MAII scorelog2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(21/1568*10)=-2.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CDK5RAP1 [Title/Abstract] AND CDH4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CDK5RAP1 [Title/Abstract] AND CDH4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CDK5RAP1(31967267)-CDH4(60503248), # samples:1
Anticipated loss of major functional domain due to fusion event.CDK5RAP1-CDH4 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.
CDK5RAP1-CDH4 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.
CDK5RAP1-CDH4 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.
CDK5RAP1-CDH4 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.
CDK5RAP1-CDH4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CDK5RAP1-CDH4 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
CDK5RAP1-CDH4 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
HgeneCDK5RAP1

GO:0045736

negative regulation of cyclin-dependent protein serine/threonine kinase activity

11882646



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/chr20:31967267/chr20:60503248)
- 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 CDK5RAP1 (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 CDH4 (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)
ENST00000346416CDK5RAP1chr2031967267-ENST00000360469CDH4chr2060503248+591312611421374410
ENST00000346416CDK5RAP1chr2031967267-ENST00000543233CDH4chr2060503248+254712611421374410
ENST00000357886CDK5RAP1chr2031967267-ENST00000360469CDH4chr2060503248+595513031421416424
ENST00000357886CDK5RAP1chr2031967267-ENST00000543233CDH4chr2060503248+258913031421416424
ENST00000544843CDK5RAP1chr2031967267-ENST00000360469CDH4chr2060503248+587112191001332410
ENST00000544843CDK5RAP1chr2031967267-ENST00000543233CDH4chr2060503248+250512191001332410

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
ENST00000346416ENST00000360469CDK5RAP1chr2031967267-CDH4chr2060503248+0.0528756450.9471243
ENST00000346416ENST00000543233CDK5RAP1chr2031967267-CDH4chr2060503248+0.033640420.96635956
ENST00000357886ENST00000360469CDK5RAP1chr2031967267-CDH4chr2060503248+0.0591409020.94085914
ENST00000357886ENST00000543233CDK5RAP1chr2031967267-CDH4chr2060503248+0.045391930.9546081
ENST00000544843ENST00000360469CDK5RAP1chr2031967267-CDH4chr2060503248+0.0527404550.9472595
ENST00000544843ENST00000543233CDK5RAP1chr2031967267-CDH4chr2060503248+0.037573150.9624269

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 CDK5RAP1-CDH4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CDK5RAP1chr2031967267CDH4chr20605032481219373RFTSPHPKDFPDEGYPRPAAPGPSRS
CDK5RAP1chr2031967267CDH4chr20605032481261373RFTSPHPKDFPDEGYPRPAAPGPSRS
CDK5RAP1chr2031967267CDH4chr20605032481303387RFTSPHPKDFPDEGYPRPAAPGPSRS

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Potential FusionNeoAntigen Information of CDK5RAP1-CDH4 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.
CDK5RAP1-CDH4_31967267_60503248.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)
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B08:09EGYPRPAA0.99950.67821220
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B45:01DEGYPRPAA0.99630.95211120
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B50:02DEGYPRPAA0.98390.81120
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B08:09EGYPRPAAP0.94120.71641221
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B18:01DEGYPRPAA0.9320.85581120
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:04FPDEGYPRP0.89910.9896918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:02FPDEGYPRP0.89910.9896918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B56:01FPDEGYPRPA0.99540.5495919
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:01HPKDFPDEGY0.98870.8023515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:08HPKDFPDEGY0.97790.8837515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B15:02HPKDFPDEGY0.96610.8688515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B50:02DEGYPRPAAP0.93350.76931121
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:05HPKDFPDEGY0.92460.6146515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B56:01FPDEGYPRPAA0.99980.6269920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B55:01FPDEGYPRPAA0.99920.5215920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:02FPDEGYPRPAA0.99490.9842920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:04FPDEGYPRPAA0.99490.9842920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:01EGYPRPAA0.99680.63311220
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B54:01FPDEGYPRP0.99520.5484918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:12FPDEGYPRP0.89910.9896918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B54:01FPDEGYPRPA0.99870.6776919
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B15:31HPKDFPDEGY0.98660.8209515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B54:01FPDEGYPRPAA0.99990.8092920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B56:04FPDEGYPRPAA0.99940.6656920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:01FPDEGYPRPAA0.99510.9633920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:12FPDEGYPRPAA0.99490.9842920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:02EGYPRPAA0.99630.7741220
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B18:05DEGYPRPAA0.9320.85581120
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B18:03DEGYPRPAA0.92020.84721120
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:09FPDEGYPRP0.89910.9896918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B59:01FPDEGYPRP0.87710.5163918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:02FPDEGYPRP0.50580.9343918
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B55:02FPDEGYPRPA0.99230.5557919
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:77HPKDFPDEGY0.98870.8023515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:20HPKDFPDEGY0.98720.8631515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:23HPKDFPDEGY0.98620.82515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:11HPKDFPDEGY0.96480.8002515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:17HPKDFPDEGY0.95770.6913515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:30HPKDFPDEGY0.95770.6913515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:24HPKDFPDEGY0.92310.84515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B15:08HPKDFPDEGY0.92030.7768515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B15:11HPKDFPDEGY0.91690.7871515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:43HPKDFPDEGY0.90280.7761515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:02FPDEGYPRPA0.82080.9712919
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B18:04HPKDFPDEGY0.52820.8515515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B18:07HPKDFPDEGY0.27690.795515
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B55:02FPDEGYPRPAA0.99980.698920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B56:02FPDEGYPRPAA0.99940.6656920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B56:05FPDEGYPRPAA0.99890.864920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B67:01FPDEGYPRPAA0.99830.9904920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B35:09FPDEGYPRPAA0.99490.9842920
CDK5RAP1-CDH4chr2031967267chr20605032481261HLA-B78:02FPDEGYPRPAA0.99340.9846920

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Potential FusionNeoAntigen Information of CDK5RAP1-CDH4 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 CDK5RAP1-CDH4

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
6715PKDFPDEGYPRPAACDK5RAP1CDH4chr2031967267chr20605032481261

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CDK5RAP1-CDH4

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-B14:023BVN6715PKDFPDEGYPRPAA-4.94269-5.69719
HLA-B14:023BVN6715PKDFPDEGYPRPAA-4.51593-4.71043
HLA-B52:013W396715PKDFPDEGYPRPAA-8.249-8.4435
HLA-B52:013W396715PKDFPDEGYPRPAA-7.17937-7.93387
HLA-A11:014UQ26715PKDFPDEGYPRPAA-8.03173-8.22623
HLA-A11:014UQ26715PKDFPDEGYPRPAA-4.95743-5.71193
HLA-A24:025HGA6715PKDFPDEGYPRPAA-6.4174-6.6119
HLA-A24:025HGA6715PKDFPDEGYPRPAA-4.65241-5.40691
HLA-B27:056PYJ6715PKDFPDEGYPRPAA-7.17858-7.93308
HLA-B27:056PYJ6715PKDFPDEGYPRPAA-3.10309-3.29759
HLA-B44:053DX86715PKDFPDEGYPRPAA-4.08639-4.28089
HLA-B44:053DX86715PKDFPDEGYPRPAA-3.78094-4.53544

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Vaccine Design for the FusionNeoAntigens of CDK5RAP1-CDH4

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
CDK5RAP1-CDH4chr2031967267chr20605032481120DEGYPRPAAGATGAGGGATACCCCCGGCCAGCGGCA
CDK5RAP1-CDH4chr2031967267chr20605032481121DEGYPRPAAPGATGAGGGATACCCCCGGCCAGCGGCACCG
CDK5RAP1-CDH4chr2031967267chr20605032481220EGYPRPAAGAGGGATACCCCCGGCCAGCGGCA
CDK5RAP1-CDH4chr2031967267chr20605032481221EGYPRPAAPGAGGGATACCCCCGGCCAGCGGCACCG
CDK5RAP1-CDH4chr2031967267chr2060503248515HPKDFPDEGYCACCCCAAGGATTTTCCTGATGAGGGATAC
CDK5RAP1-CDH4chr2031967267chr2060503248918FPDEGYPRPTTTCCTGATGAGGGATACCCCCGGCCA
CDK5RAP1-CDH4chr2031967267chr2060503248919FPDEGYPRPATTTCCTGATGAGGGATACCCCCGGCCAGCG
CDK5RAP1-CDH4chr2031967267chr2060503248920FPDEGYPRPAATTTCCTGATGAGGGATACCCCCGGCCAGCGGCA

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 CDK5RAP1-CDH4

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
LUADCDK5RAP1-CDH4chr2031967267ENST00000346416chr2060503248ENST00000360469TCGA-75-6211-01A

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Potential target of CAR-T therapy development for CDK5RAP1-CDH4

check button Predicted 3D structure. We used RoseTTAFold.
92_CDK5RAP1-CDH4_4fbd6_pred.pdb


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
TgeneCDH4chr20:31967267chr20:60503248ENST000003604691016735_7560917.0TransmembraneHelical
TgeneCDH4chr20:31967267chr20:60503248ENST00000543233915735_7560843.0TransmembraneHelical

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
CDK5RAP1chr2031967267ENST00000346416CDH4chr2060503248ENST00000360469
CDK5RAP1chr2031967267ENST00000357886CDH4chr2060503248ENST00000360469

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Related Drugs to CDK5RAP1-CDH4

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 CDK5RAP1-CDH4

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