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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: 13798

FusionGeneSummary for FOXK2_TNFSF13

check button Fusion gene summary
Fusion gene informationFusion gene name: FOXK2_TNFSF13
Fusion gene ID: 13798
HgeneTgene
Gene symbol

FOXK2

TNFSF13

Gene ID

3607

8741

Gene nameforkhead box K2TNF superfamily member 13
SynonymsILF|ILF-1|ILF1APRIL|CD256|TALL-2|TALL2|TNLG7B|TRDL-1|UNQ383/PRO715|ZTNF2
Cytomap

17q25.3

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionforkhead box protein K2FOXK1cellular transcription factor ILF-1interleukin enhancer-binding factor 1tumor necrosis factor ligand superfamily member 13TNF- and APOL-related leukocyte expressed ligand 2a proliferation-inducing ligandtumor necrosis factor (ligand) superfamily, member 13tumor necrosis factor ligand 7Btumor necrosis factor superfamily m
Modification date2018052320180519
UniProtAcc

Q01167

O75888

Ensembl transtripts involved in fusion geneENST00000335255, ENST00000529652, 
ENST00000483039, ENST00000396542, 
ENST00000349228, ENST00000338784, 
ENST00000380535, ENST00000396545, 
Fusion gene scores* DoF score25 X 11 X 12=33001 X 1 X 1=1
# samples 231
** MAII scorelog2(23/3300*10)=-3.8427602581888
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: FOXK2 [Title/Abstract] AND TNFSF13 [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
HgeneFOXK2

GO:0045944

positive regulation of transcription by RNA polymerase II

9065434

TgeneTNFSF13

GO:0048298

positive regulation of isotype switching to IgA isotypes

14988498


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
TCGALDACCTCGA-OR-A5LO-01AFOXK2chr17

80478183

+TNFSF13chr17

7463163

+
* 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-5UTRENST00000335255ENST00000483039FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
5CDS-5UTRENST00000335255ENST00000396542FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
5CDS-intronENST00000335255ENST00000349228FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
5CDS-intronENST00000335255ENST00000338784FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
5CDS-intronENST00000335255ENST00000380535FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
5CDS-intronENST00000335255ENST00000396545FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-5UTRENST00000529652ENST00000483039FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-5UTRENST00000529652ENST00000396542FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-intronENST00000529652ENST00000349228FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-intronENST00000529652ENST00000338784FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-intronENST00000529652ENST00000380535FOXK2chr17

80478183

+TNFSF13chr17

7463163

+
intron-intronENST00000529652ENST00000396545FOXK2chr17

80478183

+TNFSF13chr17

7463163

+

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FusionProtFeatures for FOXK2_TNFSF13


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FOXK2

Q01167

TNFSF13

O75888

Transcriptional regulator that recognizes the coresequence 5'-TAAACA-3'. Binds to NFAT-like motifs (purine-rich) inthe IL2 promoter (PubMed:1339390). Positively regulates WNT/beta-catenin signaling by translocating DVL proteins into the nucleus(PubMed:25805136). Also binds to HIV-1 long terminal repeat. Maybe involved in both positive and negative regulation of importantviral and cellular promoter elements (PubMed:1909027).{ECO:0000269|PubMed:1339390, ECO:0000269|PubMed:1909027,ECO:0000269|PubMed:25805136}. Cytokine that binds to TNFRSF13B/TACI and toTNFRSF17/BCMA. Plays a role in the regulation of tumor cellgrowth. May be involved in monocyte/macrophage-mediatedimmunological processes. {ECO:0000269|PubMed:10973284}.

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 FOXK2_TNFSF13


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 FOXK2_TNFSF13


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
FOXK2BAP1, AMOT, IRF2, CBX6, SOX2, HECW2, GPS2, RBBP7, SMU1, TEAD1, ESR1, BARD1, XPO1, SAP30, CTR9, HCFC1, MAX, TEAD2, FOXE1, FOXK1, SIN3A, ARID4B, BPTF, NCOR1, ARID4A, SMARCA5, TFAP4, MNT, SAP130, SUDS3, SMARCA1, ZBTB10, BRMS1L, KANSL1, TBL1XR1, ASXL2, BRMS1, MAP1B, TPR, CIC, C17orf49, LIG3, KMT2D, ASXL1, CHD4, HDAC2, ING2, MCRS1, PRDM10, RB1, RBBP5, TBP, KDM1B, DVL2, ING1, KDM5A, KANSL3, PHF20L1, CUX1, DMAP1, DRAP1, HIRA, HMGXB4, HOXD13, NCOR2, SATB2, SIN3B, TBL1X, TBL1Y, ADNP, C11orf30, KANSL2, DPY30, GTF3C3, H2AFY, HOXB9, NFYC, NRF1, NUP107, PSIP1, SAP30L, SF3B1, TP53BP1, SNX9, UBR4, RBM26, PUF60, ANKRD52, EIF2AK3, CHEK2, PRRC2C, UHRF1BP1, ANKRD28, SRPK2, CDK11A, KIAA0513, PER1, USP47, FLJ25613, TMF1, ABHD10, EIF5B, KANK2, RSRC2, FAM120A, NHP2, PHF23, SNRNP200, THRAP3, TP53, YTHDC1, HDAC1, NFATC1, DVL3, ZNF428, AHCYL2, TNFRSF1A, TULP3, FAM60A, PDGFRB, IKZF1, TP63, ZBTB39, CPD, TRIM25TNFSF13TNFSF13B, TNFSF13, TNFRSF13B, TNFRSF1A, TNFRSF14, FAS, TNFRSF11B, CAMK1D, KRAS, PIK3CA


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 FOXK2_TNFSF13


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 FOXK2_TNFSF13


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTNFSF13C0000786Spontaneous abortion1CTD_human
TgeneTNFSF13C0009404Colorectal Neoplasms1CTD_human
TgeneTNFSF13C0017661IGA Glomerulonephritis1CTD_human
TgeneTNFSF13C0036341Schizophrenia1PSYGENET