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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: 6332

FusionGeneSummary for CDC27_MYL4

check button Fusion gene summary
Fusion gene informationFusion gene name: CDC27_MYL4
Fusion gene ID: 6332
HgeneTgene
Gene symbol

CDC27

MYL4

Gene ID

996

4635

Gene namecell division cycle 27myosin light chain 4
SynonymsANAPC3|APC3|CDC27Hs|D0S1430E|D17S978E|H-NUC|HNUC|NUC2ALC1|AMLC|GT1|PRO1957
Cytomap

17q21.32

17q21.32

Type of geneprotein-codingprotein-coding
Descriptioncell division cycle protein 27 homologD0S1430E, D17S978Eanaphase promoting complex subunit 3anaphase-promoting complex, protein 3cell division cycle 27 homolognuc2 homologmyosin light chain 4myosin light chain 1, embryonic muscle/atrial isoformmyosin light chain alkali GT-1 isoformmyosin, atrial/fetal muscle, light chainmyosin, light chain 4, alkali; atrial, embryonicmyosin, light polypeptide 4, alkali; atrial, embryo
Modification date2018052320180519
UniProtAcc

P30260

P12829

Ensembl transtripts involved in fusion geneENST00000066544, ENST00000531206, 
ENST00000446365, ENST00000527547, 
ENST00000528748, 
ENST00000572316, 
ENST00000354968, ENST00000393450, 
Fusion gene scores* DoF score10 X 5 X 9=4508 X 2 X 7=112
# samples 108
** MAII scorelog2(10/450*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/112*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CDC27 [Title/Abstract] AND MYL4 [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
HgeneCDC27

GO:0070979

protein K11-linked ubiquitination

18485873


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
TCGARVPRADTCGA-HC-7213-01ACDC27chr17

45266512

-MYL4chr17

45286755

+
* 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
5CDS-5UTRENST00000066544ENST00000572316CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000066544ENST00000354968CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000066544ENST00000393450CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000531206ENST00000572316CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000531206ENST00000354968CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000531206ENST00000393450CDC27chr17

45266512

-MYL4chr17

45286755

+
5UTR-5UTRENST00000446365ENST00000572316CDC27chr17

45266512

-MYL4chr17

45286755

+
5UTR-5UTRENST00000446365ENST00000354968CDC27chr17

45266512

-MYL4chr17

45286755

+
5UTR-5UTRENST00000446365ENST00000393450CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000527547ENST00000572316CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000527547ENST00000354968CDC27chr17

45266512

-MYL4chr17

45286755

+
5CDS-5UTRENST00000527547ENST00000393450CDC27chr17

45266512

-MYL4chr17

45286755

+
intron-5UTRENST00000528748ENST00000572316CDC27chr17

45266512

-MYL4chr17

45286755

+
intron-5UTRENST00000528748ENST00000354968CDC27chr17

45266512

-MYL4chr17

45286755

+
intron-5UTRENST00000528748ENST00000393450CDC27chr17

45266512

-MYL4chr17

45286755

+

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FusionProtFeatures for CDC27_MYL4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CDC27

P30260

MYL4

P12829

Component of the anaphase promoting complex/cyclosome(APC/C), a cell cycle-regulated E3 ubiquitin ligase that controlsprogression through mitosis and the G1 phase of the cell cycle.The APC/C complex acts by mediating ubiquitination and subsequentdegradation of target proteins: it mainly mediates the formationof 'Lys-11'-linked polyubiquitin chains and, to a lower extent,the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitinchains. {ECO:0000269|PubMed:18485873}. Regulatory light chain of myosin. Does not bind calcium.

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 CDC27_MYL4


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 CDC27_MYL4


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
CDC27ANAPC1, ANAPC10, ANAPC11, ANAPC4, ANAPC5, CDC16, ANAPC7, CDC23, CDC20, SPATC1, FZR1, PPP5C, SMAD3, SMAD2, PIN1, MAD2L1, BUB1B, CDC26, CDKN1A, TTK, USP11, PTTG1, CCNB1, CTNNB1, ANAPC2, MDC1, CREBBP, HSF2, UBE2S, ANAPC16, BUB3, CKS1B, SMARCAD1, SH3KBP1, CUEDC2, RB1, NINL, FOXM1, CDC27, FBXO5, AURKB, USP37, ANAPC13, EMILIN1, MCPH1, NEK2, MAD1L1, MAD2L1BP, UBE4B, PAXIP1, TP53BP1, NOTCH1, ANAPC15, MAD2L2, REV1, TRIM33, VCP, PTEN, GKN1, DCPS, ADNP, PHF8, MIB1, HECW2, BIRC6, FBXO43, COMT, E2F1, TFDP1, CDH1, CCNA2, SIRT6, PENK, GRAP2, MAGIX, EPN3, RRM2, TTLL1, DCLRE1C, NTRK1, NCL, RPL5, TAF4, TAF5, KRAS, CFAP97, XPO1, CHD8, ZNF526, RBPJ, TEAD2, FOXE1, FOXO3, FOXP3, FOXQ1, SNW1, CDC5L, PPP2R5A, PPP2CA, PCNA, CCND1, ELMO1, ELMO2, C16orf87, ANO6, RNF19B, ZNF408, KIF2B, FDPS, SRP68, RSBN1, TACC3, NUP98, HOXD13, LNP1, HHEXMYL4ALB, FN1, VCAM1, ITGA4, PYROXD2


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 CDC27_MYL4


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 CDC27_MYL4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYL4C0007194Hypertrophic Cardiomyopathy1CTD_human