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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 30573

FusionGeneSummary for RASSF4_DES

check button Fusion gene summary
Fusion gene informationFusion gene name: RASSF4_DES
Fusion gene ID: 30573
HgeneTgene
Gene symbol

RASSF4

DES

Gene ID

83937

1674

Gene nameRas association domain family member 4desmin
SynonymsAD037CDCD3|CMD1F|CSM1|CSM2|LGMD1D|LGMD1E|LGMD2R
Cytomap

10q11.21

2q35

Type of geneprotein-codingprotein-coding
Descriptionras association domain-containing protein 4Ras association (RalGDS/AF-6) domain family 4Ras association (RalGDS/AF-6) domain family member 4Ras association domain family 4tumor suppressor RASSF4desmincardiomyopathy, dilated 1F (autosomal dominant)intermediate filament proteinmutant desmin p.K241E
Modification date2018051920180522
UniProtAcc

Q9H2L5

P17661

Ensembl transtripts involved in fusion geneENST00000334940, ENST00000374417, 
ENST00000340258, ENST00000472561, 
ENST00000373960, 
Fusion gene scores* DoF score5 X 5 X 1=254 X 5 X 2=40
# samples 55
** MAII scorelog2(5/25*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/40*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RASSF4 [Title/Abstract] AND DES [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1F00836RASSF4chr10

45471956

-DESchr2

220290894

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3UTRENST00000334940ENST00000373960RASSF4chr10

45471956

-DESchr2

220290894

-
intron-3UTRENST00000374417ENST00000373960RASSF4chr10

45471956

-DESchr2

220290894

-
intron-3UTRENST00000340258ENST00000373960RASSF4chr10

45471956

-DESchr2

220290894

-
intron-3UTRENST00000472561ENST00000373960RASSF4chr10

45471956

-DESchr2

220290894

-

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FusionProtFeatures for RASSF4_DES


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RASSF4

Q9H2L5

DES

P17661

Potential tumor suppressor. May act as a KRAS effectorprotein. May promote apoptosis and cell cycle arrest.{ECO:0000269|PubMed:15574778}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for RASSF4_DES


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for RASSF4_DES


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for RASSF4_DES


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for RASSF4_DES


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRASSF4C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneDESC1832370MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED18CTD_human;ORPHANET;UNIPROT
TgeneDESC1858154CARDIOMYOPATHY, DILATED, 1I5CTD_human;UNIPROT
TgeneDESC1867005Scapuloperoneal Syndrome, Neurogenic, Kaeser Type3CTD_human;ORPHANET;UNIPROT
TgeneDESC0004238Atrial Fibrillation1CTD_human
TgeneDESC0017658Glomerulonephritis1CTD_human
TgeneDESC0024667Animal Mammary Neoplasms1CTD_human
TgeneDESC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneDESC0027720Nephrosis1CTD_human
TgeneDESC0038356Stomach Neoplasms1CTD_human
TgeneDESC0598608Hyperhomocysteinemia1CTD_human
TgeneDESC1458155Mammary Neoplasms1CTD_human