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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: 15057

FusionGeneSummary for GOLGA8B_ACTC1

check button Fusion gene summary
Fusion gene informationFusion gene name: GOLGA8B_ACTC1
Fusion gene ID: 15057
HgeneTgene
Gene symbol

GOLGA8B

ACTC1

Gene ID

440270

70

Gene namegolgin A8 family member Bactin, alpha, cardiac muscle 1
SynonymsGOLGA5ACTC|ASD5|CMD1R|CMH11|LVNC4
Cytomap

15q14

15q14

Type of geneprotein-codingprotein-coding
Descriptiongolgin subfamily A member 8Bgolgi autoantigen, golgin subfamily a, 8Bgolgin-67actin, alpha cardiac muscle 1
Modification date2018052320180519
UniProtAcc

A8MQT2

P68032

Ensembl transtripts involved in fusion geneENST00000267731, ENST00000569811, 
ENST00000342314, ENST00000438958, 
ENST00000290378, ENST00000557860, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/8*10)=1.90689059560852
Context

PubMed: GOLGA8B [Title/Abstract] AND ACTC1 [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
TgeneACTC1

GO:0030048

actin filament-based movement

16611632


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
TCGARVESCATCGA-L5-A4OS-01AGOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
* 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
5UTR-5UTRENST00000267731ENST00000290378GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
5UTR-intronENST00000267731ENST00000557860GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-5UTRENST00000569811ENST00000290378GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-intronENST00000569811ENST00000557860GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-5UTRENST00000342314ENST00000290378GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-intronENST00000342314ENST00000557860GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-5UTRENST00000438958ENST00000290378GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-
intron-intronENST00000438958ENST00000557860GOLGA8Bchr15

34875717

-ACTC1chr15

35087031

-

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FusionProtFeatures for GOLGA8B_ACTC1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GOLGA8B

A8MQT2

ACTC1

P68032

May be involved in maintaining Golgi structure.{ECO:0000250}. Actins are highly conserved proteins that are involvedin various types of cell motility and are ubiquitously expressedin all eukaryotic cells.

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 GOLGA8B_ACTC1


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 GOLGA8B_ACTC1


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
GOLGA8BCDH1ACTC1ABLIM3, TNNI3K, SYNE2, AFAP1, ESR1, TADA2A, UCHL5, GAPDH, ARRB2, SMARCA4, CD2AP, SH3KBP1, PDCD6IP, SP1, KLHL2, TPM1, ACTA2, MYH10, MAGOH, EIF4A3, TRAF3IP1, MYC, UBL4A, ITGA4, CAPN1, PAN2, BCL11A, ERRFI1, CCDC8, AATK, DAPK1, HSPB2, MCM2, ERBB3, PHACTR2, TMOD3, NPB, TWF2, COBL, NDUFA4L2, UBC


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 GOLGA8B_ACTC1


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 GOLGA8B_ACTC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneACTC1C2677506Cardiomyopathy, Familial Hypertrophic, 114CTD_human;UNIPROT
TgeneACTC1C0032927Precancerous Conditions1CTD_human
TgeneACTC1C0034951Refractive Errors1CTD_human
TgeneACTC1C0038356Stomach Neoplasms1CTD_human
TgeneACTC1C2748552Atrial Septal Defect 51CTD_human;UNIPROT
TgeneACTC1C3150681CARDIOMYOPATHY, DILATED, 1R1UNIPROT