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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: 13613

FusionGeneSummary for FMNL2_SEC24C

check button Fusion gene summary
Fusion gene informationFusion gene name: FMNL2_SEC24C
Fusion gene ID: 13613
HgeneTgene
Gene symbol

FMNL2

SEC24C

Gene ID

114793

9632

Gene nameformin like 2SEC24 homolog C, COPII coat complex component
SynonymsFHOD2-
Cytomap

2q23.3

10q22.2

Type of geneprotein-codingprotein-coding
Descriptionformin-like protein 2formin homology 2 domain containing 2formin homology 2 domain-containing protein 2protein transport protein Sec24CSEC24 family, member CSEC24 related gene family, member CSEC24-related protein C
Modification date2018052220180522
UniProtAcc

Q96PY5

P53992

Ensembl transtripts involved in fusion geneENST00000288670, ENST00000475377, 
ENST00000497192, 
ENST00000535742, 
ENST00000546025, ENST00000345254, 
ENST00000540668, ENST00000339365, 
ENST00000411652, ENST00000496827, 
Fusion gene scores* DoF score6 X 6 X 3=1085 X 5 X 2=50
# samples 65
** MAII scorelog2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/50*10)=0
Context

PubMed: FMNL2 [Title/Abstract] AND SEC24C [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
TgeneSEC24C

GO:0090110

cargo loading into COPII-coated vesicle

17499046|18843296


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
ChiTaRS3.1BG998981FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
* 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-intronENST00000288670ENST00000535742FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000546025FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000345254FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000540668FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000339365FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000411652FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000288670ENST00000496827FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000535742FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000546025FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000345254FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000540668FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000339365FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000411652FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000475377ENST00000496827FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000535742FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000546025FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000345254FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000540668FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000339365FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000411652FMNL2chr2

153300686

+SEC24Cchr10

75526109

+
intron-intronENST00000497192ENST00000496827FMNL2chr2

153300686

+SEC24Cchr10

75526109

+

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FusionProtFeatures for FMNL2_SEC24C


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FMNL2

Q96PY5

SEC24C

P53992

Plays a role in the regulation of cell morphology andcytoskeletal organization. Required in the cortical actin filamentdynamics. {ECO:0000269|PubMed:21834987}. Component of the coat protein complex II (COPII) whichpromotes the formation of transport vesicles from the endoplasmicreticulum (ER). The coat has two main functions, the physicaldeformation of the endoplasmic reticulum membrane into vesiclesand the selection of cargo molecules for their transport to theGolgi complex (PubMed:10214955, PubMed:17499046, PubMed:18843296,PubMed:20427317). Plays a central role in cargo selection withinthe COPII complex and together with SEC24D may have a differentspecificity compared to SEC24A and SEC24B (PubMed:17499046,PubMed:20427317, PubMed:18843296). May more specifically packageGPI-anchored proteins through the cargo receptor TMED10(PubMed:20427317). May also be specific for IxM motif-containingcargos like the SNAREs GOSR2 and STX5 (PubMed:18843296).{ECO:0000269|PubMed:10214955, ECO:0000269|PubMed:17499046,ECO:0000269|PubMed:18843296, ECO:0000269|PubMed:20427317}.

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 FMNL2_SEC24C


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 FMNL2_SEC24C


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 FMNL2_SEC24C


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 FMNL2_SEC24C


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSEC24CC0005586Bipolar Disorder1PSYGENET
TgeneSEC24CC0041696Unipolar Depression1PSYGENET
TgeneSEC24CC1269683Major Depressive Disorder1PSYGENET