FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 23976

FusionGeneSummary for NEDD9_CLINT1

check button Fusion gene summary
Fusion gene informationFusion gene name: NEDD9_CLINT1
Fusion gene ID: 23976
HgeneTgene
Gene symbol

NEDD9

CLINT1

Gene ID

4739

9685

Gene nameneural precursor cell expressed, developmentally down-regulated 9clathrin interactor 1
SynonymsCAS-L|CAS2|CASL|CASS2|HEF1CLINT|ENTH|EPN4|EPNR
Cytomap

6p24.2

5q33.3

Type of geneprotein-codingprotein-coding
Descriptionenhancer of filamentation 1Cas scaffolding protein family member 2Crk-associated substrate related protein Cas-LEnhancer of filamentation 1 p55cas-like dockingneural precursor cell expressed developmentally down-regulated protein 9p130Cas-related prclathrin interactor 1clathrin interacting protein localized in the trans-Golgi regionenthoprotinepsin 4epsin-related proteinepsinR
Modification date2018052320180522
UniProtAcc

Q14511

Q14677

Ensembl transtripts involved in fusion geneENST00000504387, ENST00000379446, 
ENST00000379433, ENST00000508800, 
ENST00000523094, ENST00000530742, 
ENST00000296951, ENST00000411809, 
ENST00000523908, 
Fusion gene scores* DoF score6 X 5 X 5=1504 X 5 X 2=40
# samples 65
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
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: NEDD9 [Title/Abstract] AND CLINT1 [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
ChiTaRS3.1AW858887NEDD9chr6

11186909

+CLINT1chr5

157263679

-
* 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-intronENST00000504387ENST00000523094NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000504387ENST00000530742NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000504387ENST00000296951NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000504387ENST00000411809NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000504387ENST00000523908NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379446ENST00000523094NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379446ENST00000530742NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379446ENST00000296951NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379446ENST00000411809NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379446ENST00000523908NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379433ENST00000523094NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379433ENST00000530742NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379433ENST00000296951NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379433ENST00000411809NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000379433ENST00000523908NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000508800ENST00000523094NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000508800ENST00000530742NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000508800ENST00000296951NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000508800ENST00000411809NEDD9chr6

11186909

+CLINT1chr5

157263679

-
intron-intronENST00000508800ENST00000523908NEDD9chr6

11186909

+CLINT1chr5

157263679

-

Top

FusionProtFeatures for NEDD9_CLINT1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NEDD9

Q14511

CLINT1

Q14677

Docking protein which plays a central coordinating rolefor tyrosine-kinase-based signaling related to cell adhesion. Mayfunction in transmitting growth control signals between focaladhesions at the cell periphery and the mitotic spindle inresponse to adhesion or growth factor signals initiating cellproliferation. May play an important role in integrin beta-1 or Bcell antigen receptor (BCR) mediated signaling in B- and T-cells.Integrin beta-1 stimulation leads to recruitment of variousproteins including CRK, NCK and SHPTP2 to the tyrosinephosphorylated form. Binds to membranes enriched in phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). May have a role in transport viaclathrin-coated vesicles from the trans-Golgi network toendosomes. Stimulates clathrin assembly.{ECO:0000269|PubMed:12429846, ECO:0000269|PubMed:12538641}.

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


Top

FusionGeneSequence for NEDD9_CLINT1


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).

Top

FusionGenePPI for NEDD9_CLINT1


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


Top

RelatedDrugs for NEDD9_CLINT1


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

Top

RelatedDiseases for NEDD9_CLINT1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource