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: 8961

FusionGeneSummary for CTU2_MLYCD

check button Fusion gene summary
Fusion gene informationFusion gene name: CTU2_MLYCD
Fusion gene ID: 8961
HgeneTgene
Gene symbol

CTU2

MLYCD

Gene ID

348180

23417

Gene namecytosolic thiouridylase subunit 2malonyl-CoA decarboxylase
SynonymsC16orf84|NCS2|UPF0432MCD
Cytomap

16q24.3

16q23.3

Type of geneprotein-codingprotein-coding
Descriptioncytoplasmic tRNA 2-thiolation protein 2cytosolic thiouridylase subunit 2 homologmalonyl-CoA decarboxylase, mitochondrialmalonyl coenzyme A decarboxylase
Modification date2018052320180522
UniProtAcc

Q2VPK5

O95822

Ensembl transtripts involved in fusion geneENST00000453996, ENST00000378384, 
ENST00000312060, ENST00000567949, 
ENST00000262430, 
Fusion gene scores* DoF score3 X 3 X 3=272 X 2 X 2=8
# samples 32
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: CTU2 [Title/Abstract] AND MLYCD [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
TgeneMLYCD

GO:0006085

acetyl-CoA biosynthetic process

9869665|10417274|10455107

TgeneMLYCD

GO:0006633

fatty acid biosynthetic process

15003260

TgeneMLYCD

GO:2001294

malonyl-CoA catabolic process

10417274|10455107|15003260


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
TCGALDBRCATCGA-BH-A1FD-01ACTU2chr16

88779313

+MLYCDchr16

83945823

+
* 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
Frame-shiftENST00000453996ENST00000262430CTU2chr16

88779313

+MLYCDchr16

83945823

+
Frame-shiftENST00000378384ENST00000262430CTU2chr16

88779313

+MLYCDchr16

83945823

+
Frame-shiftENST00000312060ENST00000262430CTU2chr16

88779313

+MLYCDchr16

83945823

+
Frame-shiftENST00000567949ENST00000262430CTU2chr16

88779313

+MLYCDchr16

83945823

+

Top

FusionProtFeatures for CTU2_MLYCD


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CTU2

Q2VPK5

MLYCD

O95822

Plays a central role in 2-thiolation of mcm(5)S(2)U attRNA wobble positions of tRNA(Lys), tRNA(Glu) and tRNA(Gln). Mayact by forming a heterodimer with CTU1/ATPBD3 that ligates sulfurfrom thiocarboxylated URM1 onto the uridine of tRNAs at wobbleposition. {ECO:0000255|HAMAP-Rule:MF_03054,ECO:0000269|PubMed:19017811}. Catalyzes the conversion of malonyl-CoA to acetyl-CoA.In the fatty acid biosynthesis MCD selectively removes malonyl-CoAand thus assures that methyl-malonyl-CoA is the only chainelongating substrate for fatty acid synthase and that fatty acidswith multiple methyl side chains are produced. In peroxisomes itmay be involved in degrading intraperoxisomal malonyl-CoA, whichis generated by the peroxisomal beta-oxidation of odd chain-lengthdicarboxylic fatty acids. Plays a role in the metabolic balancebetween glucose and lipid oxidation in muscle independent ofalterations in insulin signaling. May play a role in controllingthe extent of ischemic injury by promoting glucose oxidation.{ECO:0000269|PubMed:10455107, ECO:0000269|PubMed:15003260,ECO:0000269|PubMed:18314420, ECO:0000269|PubMed:23482565}.

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 CTU2_MLYCD


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 CTU2_MLYCD


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
CTU2CTU1, MMS19, FAM96B, CIAO1, KLHL20, WISP2, UROS, KCTD17, RRAGA, NFKBIA, FAS, FAM219A, VAPB, CCNDBP1, LBHD1, TINAG, MYCL, THUMPD3, ZMAT5, CCDC120, PFDN4, POLM, RAB8B, RGS20, FAM174A, CEP72, APEX2, FAM19A3, SLC5A5, PROSER2MLYCDPEX5, FYCO1, COQ6, ADCK1, PCDHGA5, PCDHA9, PCDHA10, PCDHA12, PCDHA3, SNX9


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 CTU2_MLYCD


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 CTU2_MLYCD


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