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: 5840

FusionGeneSummary for CCDC28B_PLEKHG1

check button Fusion gene summary
Fusion gene informationFusion gene name: CCDC28B_PLEKHG1
Fusion gene ID: 5840
HgeneTgene
Gene symbol

CCDC28B

PLEKHG1

Gene ID

79140

57480

Gene namecoiled-coil domain containing 28Bpleckstrin homology and RhoGEF domain containing G1
Synonyms-ARHGEF41
Cytomap

1p35.2

6q25.1

Type of geneprotein-codingprotein-coding
Descriptioncoiled-coil domain-containing protein 28Bpleckstrin homology domain-containing family G member 1pleckstrin homology domain containing, family G (with RhoGef domain) member 1
Modification date2018052320180519
UniProtAcc

Q9BUN5

Q9ULL1

Ensembl transtripts involved in fusion geneENST00000373602, ENST00000421922, 
ENST00000483009, 
ENST00000367328, 
ENST00000358517, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 8 X 4=224
# samples 18
** MAII scorelog2(1/1*10)=3.32192809488736log2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCDC28B [Title/Abstract] AND PLEKHG1 [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
ChiTaRS3.1AA344455CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
* 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-intronENST00000373602ENST00000367328CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
intron-intronENST00000373602ENST00000358517CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
3UTR-intronENST00000421922ENST00000367328CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
3UTR-intronENST00000421922ENST00000358517CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
intron-intronENST00000483009ENST00000367328CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+
intron-intronENST00000483009ENST00000358517CCDC28Bchr1

32670632

-PLEKHG1chr6

151003671

+

Top

FusionProtFeatures for CCDC28B_PLEKHG1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CCDC28B

Q9BUN5

PLEKHG1

Q9ULL1

Involved in ciliogenesis. Regulates cilia length throughits interaction with MAPKAP1/SIN1 but independently of mTORC2complex. Modulates mTORC2 complex assembly and function, possiblyenhances AKT1 phosphorylation. Does not seem to modulate assemblyand function of mTORC1 complex. {ECO:0000269|PubMed:23015189,ECO:0000269|PubMed:23727834}.

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 CCDC28B_PLEKHG1


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 CCDC28B_PLEKHG1


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 CCDC28B_PLEKHG1


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 CCDC28B_PLEKHG1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePLEKHG1C0040336Tobacco Use Disorder1CTD_human