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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: 23168

FusionGeneSummary for MYO5B_CCDC11

check button Fusion gene summary
Fusion gene informationFusion gene name: MYO5B_CCDC11
Fusion gene ID: 23168
HgeneTgene
Gene symbol

MYO5B

CCDC11

Gene ID

4645

220136

Gene namemyosin VBcilia and flagella associated protein 53
Synonyms-CCDC11|HTX6
Cytomap

18q21.1

18q21.1

Type of geneprotein-codingprotein-coding
Descriptionunconventional myosin-VbMYO5B variant proteinmyosin-Vbcilia- and flagella-associated protein 53coiled-coil domain containing 11
Modification date2018051920180519
UniProtAcc

Q9ULV0

Ensembl transtripts involved in fusion geneENST00000285039, ENST00000324581, 
ENST00000592688, ENST00000587895, 
ENST00000398545, 
Fusion gene scores* DoF score8 X 4 X 6=1922 X 2 X 2=8
# samples 82
** MAII scorelog2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: MYO5B [Title/Abstract] AND CCDC11 [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
TCGARVBLCATCGA-GV-A3JZ-01AMYO5Bchr18

47721137

-CCDC11chr18

47788589

-
* 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
In-frameENST00000285039ENST00000398545MYO5Bchr18

47721137

-CCDC11chr18

47788589

-
intron-3CDSENST00000324581ENST00000398545MYO5Bchr18

47721137

-CCDC11chr18

47788589

-
intron-3CDSENST00000592688ENST00000398545MYO5Bchr18

47721137

-CCDC11chr18

47788589

-
intron-3CDSENST00000587895ENST00000398545MYO5Bchr18

47721137

-CCDC11chr18

47788589

-

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FusionProtFeatures for MYO5B_CCDC11


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYO5B

Q9ULV0

CCDC11

May be involved in vesicular trafficking via itsassociation with the CART complex. The CART complex is necessaryfor efficient transferrin receptor recycling but not for EGFRdegradation. Required in a complex with RAB11A and RAB11FIP2 forthe transport of NPC1L1 to the plasma membrane. Together withRAB11A participates in CFTR trafficking to the plasma membrane andTF (transferrin) recycling in nonpolarized cells. Together withRAB11A and RAB8A participates in epithelial cell polarization.Together with RAB25 regulates transcytosis.{ECO:0000269|PubMed:21206382, ECO:0000269|PubMed:21282656}. Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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
TgeneCCDC11chr18:47721137chr18:47788589ENST00000398545-08203_47423515Coiled coilOntology_term=ECO:0000255
TgeneCCDC11chr18:47721137chr18:47788589ENST00000398545-0891_14823515Coiled coilOntology_term=ECO:0000255

- In-frame and not-retained protein feature among the 13 regional features.
>>>>>>>>>>>>>>
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-1401341_147191849Coiled coilOntology_term=ECO:0000255
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140899_126691849Coiled coilOntology_term=ECO:0000255
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140801_91691849Compositional biasNote=Arg-rich
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-1401526_180391849DomainDilute
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-14069_76191849DomainMyosin motor
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140769_79891849DomainIQ 1
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140792_82191849DomainIQ 2
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140817_84891849DomainIQ 3
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140840_86991849DomainIQ 4
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140865_89691849DomainIQ 5
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140888_91791849DomainIQ 6
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-1408_6091849DomainMyosin N-terminal SH3-like
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140163_17091849Nucleotide bindingATP
HgeneMYO5Bchr18:47721137chr18:47788589ENST00000285039-140640_66291849RegionActin-binding


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FusionGeneSequence for MYO5B_CCDC11


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 MYO5B_CCDC11


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
MYO5BCXCR2, RAB11FIP2, KIAA1549, COIL, PAN2, RAB11A, RAB11B, RAB25, RAB8A, POLR1C, BNIP2, TCF4, AMOTL2, TRIM54, CCDC8, PEX19, LRRC39, TMOD1, CAPZB, CAPZA2, DBN1, MYH9, PPP1CB, IQGAP1, SYNPO, LIMA1, ANLN, MYO19, SKA3, MYO18A, EXOC6, SYTL4, RAB3B, STX3, TBC1D30, EVI5, SSH1, TMOD3, DKK3, MYL2, PPP6R2, PDF, RAC1, TRIM25CCDC11


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 MYO5B_CCDC11


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 MYO5B_CCDC11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYO5BC0341306Microvillus inclusion disease5CTD_human;ORPHANET;UNIPROT
HgeneMYO5BC0011991Diarrhea1CTD_human
HgeneMYO5BC0021831Intestinal Diseases1CTD_human
HgeneMYO5BC0023903Liver neoplasms1CTD_human
HgeneMYO5BC0025521Inborn Errors of Metabolism1CTD_human
HgeneMYO5BC0036341Schizophrenia1PSYGENET
HgeneMYO5BC0236733Amphetamine-Related Disorders1CTD_human
HgeneMYO5BC0525045Mood Disorders1PSYGENET