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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: 13346

FusionGeneSummary for FGD4_DNM1L

check button Fusion gene summary
Fusion gene informationFusion gene name: FGD4_DNM1L
Fusion gene ID: 13346
HgeneTgene
Gene symbol

FGD4

DNM1L

Gene ID

121512

10059

Gene nameFYVE, RhoGEF and PH domain containing 4dynamin 1 like
SynonymsCMT4H|FRABP|ZFYVE6DLP1|DRP1|DVLP|DYMPLE|EMPF|EMPF1|HDYNIV|OPA5
Cytomap

12p11.21

12p11.21

Type of geneprotein-codingprotein-coding
DescriptionFYVE, RhoGEF and PH domain-containing protein 4FGD1 family, member 4FGD1-related F-actin-binding proteinactin-filament binding protein frabinzinc finger FYVE domain-containing protein 6dynamin-1-like proteinDnm1p/Vps1p-like proteindynamin family member proline-rich carboxyl-terminal domain lessdynamin-like protein 4dynamin-like protein IVdynamin-related protein 1
Modification date2018051920180523
UniProtAcc

Q96M96

O00429

Ensembl transtripts involved in fusion geneENST00000534526, ENST00000531134, 
ENST00000427716, ENST00000266482, 
ENST00000546442, ENST00000525053, 
ENST00000381025, ENST00000472289, 
ENST00000473513, 
ENST00000452533, 
ENST00000553257, ENST00000549701, 
ENST00000358214, ENST00000548671, 
ENST00000266481, ENST00000547312, 
ENST00000414834, ENST00000381000, 
Fusion gene scores* DoF score14 X 9 X 12=15127 X 6 X 7=294
# samples 158
** MAII scorelog2(15/1512*10)=-3.33342373372519
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/294*10)=-1.877744249949
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FGD4 [Title/Abstract] AND DNM1L [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
TgeneDNM1L

GO:0000266

mitochondrial fission

23530241

TgeneDNM1L

GO:0003374

dynamin family protein polymerization involved in mitochondrial fission

11514614|23530241

TgeneDNM1L

GO:0016559

peroxisome fission

12618434

TgeneDNM1L

GO:0032459

regulation of protein oligomerization

20850011

TgeneDNM1L

GO:0050714

positive regulation of protein secretion

9570752

TgeneDNM1L

GO:0051289

protein homotetramerization

18353969

TgeneDNM1L

GO:0061025

membrane fusion

20850011

TgeneDNM1L

GO:0090149

mitochondrial membrane fission

11514614


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
TCGALDLUADTCGA-38-4630-01AFGD4chr12

32552893

+DNM1Lchr12

32884788

+
* 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
Frame-shiftENST00000534526ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
Frame-shiftENST00000534526ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
Frame-shiftENST00000534526ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
Frame-shiftENST00000534526ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
5CDS-intronENST00000534526ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
5CDS-intronENST00000534526ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
5CDS-intronENST00000534526ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
5CDS-intronENST00000534526ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
5CDS-intronENST00000534526ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000531134ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000531134ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000531134ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000531134ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000531134ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000531134ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000531134ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000531134ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000531134ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000427716ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000427716ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000427716ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000427716ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000427716ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000427716ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000427716ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000427716ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000427716ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000266482ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000266482ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000266482ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000266482ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000266482ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000266482ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000266482ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000266482ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000266482ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000546442ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000546442ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000546442ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000546442ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000546442ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000546442ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000546442ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000546442ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000546442ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000525053ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000525053ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000525053ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000525053ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000525053ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000525053ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000525053ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000525053ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000525053ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000381025ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000381025ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000381025ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000381025ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000381025ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000381025ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000381025ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000381025ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000381025ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000472289ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000472289ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000472289ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000472289ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000472289ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000472289ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000472289ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000472289ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000472289ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000473513ENST00000452533FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000473513ENST00000553257FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000473513ENST00000549701FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-3CDSENST00000473513ENST00000358214FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000473513ENST00000548671FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000473513ENST00000266481FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000473513ENST00000547312FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000473513ENST00000414834FGD4chr12

32552893

+DNM1Lchr12

32884788

+
intron-intronENST00000473513ENST00000381000FGD4chr12

32552893

+DNM1Lchr12

32884788

+

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FusionProtFeatures for FGD4_DNM1L


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FGD4

Q96M96

DNM1L

O00429

Activates CDC42, a member of the Ras-like family ofRho- and Rac proteins, by exchanging bound GDP for free GTP. Playsa role in regulating the actin cytoskeleton and cell shape.Activates MAPK8 (By similarity). {ECO:0000250,ECO:0000269|PubMed:15133042}.

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 FGD4_DNM1L


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 FGD4_DNM1L


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
FGD4CAPZA2, FGD3, PRKCADNM1LGSK3B, FIS1, PEX11A, PEX11B, PEX11G, PARK2, GABRR1, MUL1, COPS5, LRRK2, MIEF1, PEX14, MARCH5, DNM1L, MFF, MIEF2, SOX2, APEH, CYHR1, CARS, ARFIP1, ATP6V1C1, TBC1D15, FAM129B, JMJD6, PSMG3, SEC24A, SSB, VPS26A, EGFR, MAGEA1, MAGEA3, RRM2, SCG3, SH3GL1, ZBTB24, FZR1, HAX1, NUFIP1, DGUOK, DNAAF2, FGL1, UNK, ATIC, TES, NTRK1, PINK1, LLGL2, PPIA, CDCA5, SNW1, CDC5L, CPNE2, CA14, DUSP23, MYL12A, PFN1, LDHB, RPL30, DBN1, NME1, CKB, TPI1, ALDOA, SAP18, CCT8, RPL12, TXN, EEF2, YWHAE, YWHAZ, YWHAB, HPRT1, CCT2, ARF1, LDHA, EIF5A, RPL27, MDH2, PRDX6, PSMC5, HNRNPA1L2, EEF1B2, PRDX2, RUVBL2, PSMC3, UBA1, EEF1G, TIMM13, VCP, RUVBL1, SF3B6, ACTN4, TPM1, SUB1, XRCC6, HSD17B10, HNRNPAB, PABPC1, HSPA4, HNRNPDL, ILF2, C14orf166, EEF1D, PAICS, YWHAQ, AHCY, PDIA6, STIP1, HSP90B1, IMPDH2, RNPS1, TAGLN2, ACLY, KPNB1, PGAM1, CDC37, PCMT1, NAP1L1, RPL28, ACTR1A, SUMO2, CCT7, TKT, EIF3F, ERH, SERBP1, RBBP4, PARK7, DCD, PSMC6, RANBP1, RARS, PTBP1, UBE2L3, EIF4A3, PDHB, PSMA4, RPA3, PLS3, GFAP, PSMC2, NACA, KCTD12, PSMC1, TRIM28, DNAJA1, HSPH1, HNRNPH3, DCTN2, RBM8A, SAE1, PRMT1, MTHFD1, PSMD2, RBMXL2, EIF2S1, EIF3D, ACTN1, SKP1, FASN, XRCC5, EZR, EIF3B, PFDN2, AHSA1, DDX21, DARS, PNN, BUB3, ACIN1, MYH11, RCC1, EIF3A, DDX39B, PSMC4, DYNC1H1, CDK1, LARS, MAT2A, TLN1, ABCE1, GANAB, CAPRIN1, IQGAP1, SAFB, SOD1, HIST1H2AE, HIST1H2AB, CKMT1B, CKMT1A, CALM1, CALM2, CALM3


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 FGD4_DNM1L


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 FGD4_DNM1L


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFGD4C1836336CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H2CTD_human;ORPHANET;UNIPROT
TgeneDNM1LC3280660ENCEPHALOPATHY, LETHAL, DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION2ORPHANET;UNIPROT
TgeneDNM1LC0001125Acidosis, Lactic1CTD_human;HPO
TgeneDNM1LC0025958Microcephaly1CTD_human
TgeneDNM1LC0029124Optic Atrophy1CTD_human;HPO
TgeneDNM1LC0151744Myocardial Ischemia1CTD_human
TgeneDNM1LC0162666Mitochondrial Encephalomyopathies1CTD_human