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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:STK11-HOXD4 (FusionGDB2 ID:86846)

Fusion Gene Summary for STK11-HOXD4

check button Fusion gene summary
Fusion gene informationFusion gene name: STK11-HOXD4
Fusion gene ID: 86846
HgeneTgene
Gene symbol

STK11

HOXD4

Gene ID

6794

3233

Gene nameserine/threonine kinase 11homeobox D4
SynonymsLKB1|PJS|hLKB1HHO.C13|HOX-5.1|HOX4|HOX4B|Hox-4.2
Cytomap

19p13.3

2q31.1

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase STK11liver kinase B1polarization-related protein LKB1renal carcinoma antigen NY-REN-19serine/threonine-protein kinase 11serine/threonine-protein kinase LKB1homeobox protein Hox-D4Hox-4.2, mouse, homolog of homeo box Xhomeobox protein HHO.C13homeobox protein Hox-4Bhomeobox protein Hox-5.1
Modification date2020032920200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000585748, ENST00000326873, 
ENST00000306324, 
Fusion gene scores* DoF score13 X 3 X 8=3122 X 1 X 1=2
# samples 172
** MAII scorelog2(17/312*10)=-0.876011282724546
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/2*10)=3.32192809488736
Context

PubMed: STK11 [Title/Abstract] AND HOXD4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSTK11(1207202)-HOXD4(177017335), # samples:1
Anticipated loss of major functional domain due to fusion event.STK11-HOXD4 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
STK11-HOXD4 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
STK11-HOXD4 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
STK11-HOXD4 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
STK11-HOXD4 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
STK11-HOXD4 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
* 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
HgeneSTK11

GO:0006468

protein phosphorylation

12805220|25329316

HgeneSTK11

GO:0007050

cell cycle arrest

12805220|17216128

HgeneSTK11

GO:0046777

protein autophosphorylation

11430832

HgeneSTK11

GO:0071493

cellular response to UV-B

25329316

HgeneSTK11

GO:0072332

intrinsic apoptotic signaling pathway by p53 class mediator

11430832

TgeneHOXD4

GO:0045944

positive regulation of transcription by RNA polymerase II

1756725


check buttonFusion gene breakpoints across STK11 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across HOXD4 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4OVTCGA-13-0724STK11chr19

1207202

+HOXD4chr2

177017335

+


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Fusion Gene ORF analysis for STK11-HOXD4

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
intron-3CDSENST00000585748ENST00000306324STK11chr19

1207202

+HOXD4chr2

177017335

+
Frame-shiftENST00000326873ENST00000306324STK11chr19

1207202

+HOXD4chr2

177017335

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for STK11-HOXD4


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
STK11chr191207202+HOXD4chr2177017335+0.0002258610.99977416
STK11chr191207202+HOXD4chr2177017335+0.0002258610.99977416

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for STK11-HOXD4


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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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Fusion Gene Sequence for STK11-HOXD4


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for STK11-HOXD4


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


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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Related Drugs for STK11-HOXD4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for STK11-HOXD4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSTK11C0031269Peutz-Jeghers Syndrome19CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneSTK11C1336708Testicular Germ Cell Tumor2CTD_human;UNIPROT
HgeneSTK11C0001418Adenocarcinoma1CTD_human
HgeneSTK11C0007137Squamous cell carcinoma1CTD_human
HgeneSTK11C0020538Hypertensive disease1CTD_human
HgeneSTK11C0024121Lung Neoplasms1CTD_human
HgeneSTK11C0030297Pancreatic Neoplasm1CGI;CTD_human
HgeneSTK11C0149721Left Ventricular Hypertrophy1CTD_human
HgeneSTK11C0152013Adenocarcinoma of lung (disorder)1CGI;CTD_human
HgeneSTK11C0205641Adenocarcinoma, Basal Cell1CTD_human
HgeneSTK11C0205642Adenocarcinoma, Oxyphilic1CTD_human
HgeneSTK11C0205643Carcinoma, Cribriform1CTD_human
HgeneSTK11C0205644Carcinoma, Granular Cell1CTD_human
HgeneSTK11C0205645Adenocarcinoma, Tubular1CTD_human
HgeneSTK11C0242379Malignant neoplasm of lung1CTD_human;UNIPROT
HgeneSTK11C0282207Cronkhite-Canada Syndrome1CTD_human
HgeneSTK11C0346647Malignant neoplasm of pancreas1CGI;CTD_human
HgeneSTK11C0887833Carcinoma, Pancreatic Ductal1CTD_human
HgeneSTK11C1257915Intestinal Polyposis1CTD_human
TgeneHOXD4C0023452Childhood Acute Lymphoblastic Leukemia1CTD_human
TgeneHOXD4C0023453L2 Acute Lymphoblastic Leukemia1CTD_human
TgeneHOXD4C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human