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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: 22129

FusionGeneSummary for MLEC_STX2

check button Fusion gene summary
Fusion gene informationFusion gene name: MLEC_STX2
Fusion gene ID: 22129
HgeneTgene
Gene symbol

MLEC

STX2

Gene ID

9761

2054

Gene namemalectinsyntaxin 2
SynonymsKIAA0152EPIM|EPM|STX2A|STX2B|STX2C
Cytomap

12q24.31

12q24.33

Type of geneprotein-codingprotein-coding
Descriptionmalectinoligosaccharyltransferase complex subunit (non-catalytic)syntaxin-2epimorphin
Modification date2018051920180523
UniProtAcc

Q14165

P32856

Ensembl transtripts involved in fusion geneENST00000228506, ENST00000412616, 
ENST00000535413, 
ENST00000261653, 
ENST00000392373, 
Fusion gene scores* DoF score3 X 4 X 2=242 X 2 X 2=8
# samples 42
** MAII scorelog2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: MLEC [Title/Abstract] AND STX2 [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
TgeneSTX2

GO:0033194

response to hydroperoxide

22226963

TgeneSTX2

GO:0051259

protein complex oligomerization

22226963

TgeneSTX2

GO:1903575

cornified envelope assembly

22226963


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
TCGARVSARCTCGA-QC-AA9N-01AMLECchr12

121125334

+STX2chr12

131306333

-
* 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-shiftENST00000228506ENST00000261653MLECchr12

121125334

+STX2chr12

131306333

-
Frame-shiftENST00000228506ENST00000392373MLECchr12

121125334

+STX2chr12

131306333

-
Frame-shiftENST00000412616ENST00000261653MLECchr12

121125334

+STX2chr12

131306333

-
Frame-shiftENST00000412616ENST00000392373MLECchr12

121125334

+STX2chr12

131306333

-
intron-3CDSENST00000535413ENST00000261653MLECchr12

121125334

+STX2chr12

131306333

-
intron-3CDSENST00000535413ENST00000392373MLECchr12

121125334

+STX2chr12

131306333

-

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FusionProtFeatures for MLEC_STX2


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

Q14165

STX2

P32856

Carbohydrate-binding protein with a strong ligandpreference for Glc2-N-glycan. May play a role in the early stepsof protein N-glycosylation (By similarity). {ECO:0000250}. Essential for epithelial morphogenesis. May mediateCa(2+)-regulation of exocytosis acrosomal reaction in sperm.

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 MLEC_STX2


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 MLEC_STX2


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
MLECELAVL1, RPS16, CTSD, RBM8A, HERC2, TCTN2, TCTN3, CEP152, SCLT1, TCTN1, TSNAX, RAB7A, GOLT1B, MCM2, MCM5, TMEM258, RPN2, STT3B, DLST, TRIM25STX2SNAP23, VAMP8, VAMP2, VAMP3, STXBP3, STXBP1, VAPB, SYT1, SNAP25, ELAVL1, ENO1, MOV10, NXF1, SYTL4, TP53


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 MLEC_STX2


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 MLEC_STX2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSTX2C0021364Male infertility1CTD_human