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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: 19241

FusionGeneSummary for KRT14_TYK2

check button Fusion gene summary
Fusion gene informationFusion gene name: KRT14_TYK2
Fusion gene ID: 19241
HgeneTgene
Gene symbol

KRT14

TYK2

Gene ID

3861

7297

Gene namekeratin 14tyrosine kinase 2
SynonymsCK14|EBS3|EBS4|K14|NFJIMD35|JTK1
Cytomap

17q21.2

19p13.2

Type of geneprotein-codingprotein-coding
Descriptionkeratin, type I cytoskeletal 14cytokeratin 14keratin 14, type Inon-receptor tyrosine-protein kinase TYK2
Modification date2018052020180522
UniProtAcc

P02533

P29597

Ensembl transtripts involved in fusion geneENST00000167586, ENST00000264818, 
ENST00000524462, ENST00000525621, 
ENST00000529370, ENST00000529422, 
Fusion gene scores* DoF score5 X 1 X 3=1542 X 7 X 17=4998
# samples 643
** MAII scorelog2(6/15*10)=2
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(43/4998*10)=-3.53894233649724
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KRT14 [Title/Abstract] AND TYK2 [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
HgeneKRT14

GO:0007568

aging

21916889

HgeneKRT14

GO:0042633

hair cycle

21916889


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
TCGARVHNSCTCGA-IQ-A61E-01AKRT14chr17

39738531

-TYK2chr19

10491352

-
* 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-intronENST00000167586ENST00000264818KRT14chr17

39738531

-TYK2chr19

10491352

-
5CDS-intronENST00000167586ENST00000524462KRT14chr17

39738531

-TYK2chr19

10491352

-
5CDS-intronENST00000167586ENST00000525621KRT14chr17

39738531

-TYK2chr19

10491352

-
5CDS-intronENST00000167586ENST00000529370KRT14chr17

39738531

-TYK2chr19

10491352

-
5CDS-intronENST00000167586ENST00000529422KRT14chr17

39738531

-TYK2chr19

10491352

-

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FusionProtFeatures for KRT14_TYK2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KRT14

P02533

TYK2

P29597

The nonhelical tail domain is involved in promotingKRT5-KRT14 filaments to self-organize into large bundles andenhances the mechanical properties involved in resilience ofkeratin intermediate filaments in vitro.{ECO:0000269|PubMed:11724817}. Probably involved in intracellular signal transductionby being involved in the initiation of type I IFN signaling.Phosphorylates the interferon-alpha/beta receptor alpha chain.{ECO:0000269|PubMed:7526154}.

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 KRT14_TYK2


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 KRT14_TYK2


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
KRT14PKP1, APC, POU5F1, PTEN, CUL3, CUL4B, CUL5, CUL2, CUL1, COPS5, CAND1, NEDD8, MDM2, INPPL1, CBL, UBASH3B, GRB2, PIK3R2, SHC1, CRK, EPS15, AP2M1, KRT5, KRT3, HNRNPC, EVPL, HNRNPU, MAGOH, EIF4A3, ALB, IQCB1, HSPA5, CUL7, OBSL1, CCDC8, RPS6KB2, HNRNPA1, PTPRN2, CYLD, UBE2ATYK2GNB2L1, STAT1, PRMT5, XRCC5, VAV1, IFNAR1, CRKL, JAK1, TYK2, ELP2, IL13RA1, LYN, CBL, PTPN6, PLAUR, IL6ST, FYN, PTPN1, STAM2, GHR, IRS2, DNM2, TK1, SOCS1, KLF10, LNX1, PTAFR, EIF2AK2, HSP90AA1, JAK3, COPS5, FHL3, HNRNPK, TRAF4, KRT40, KHDRBS2, SIVA1, SHMT2, MOV10, NXF1, BAG2, CCT2, CCT3, CCT4, CCT5, CCT6A, CCT7, CCT8, DDX5, HNRNPH1, HSPB1, CEP170B, RAN, RUVBL1, RUVBL2, SLC2A1, TCP1, ALYREF, TRIM28, TUBA4A, WDR20, EFNB2, PIH1D1, TGFBR2, LRRC46, LPAR6, RNF13, ZNF333, MIER2, SIAH2, UBE2L6, LRP8, IFT43, PMEL, TNFRSF19, GMNN, IL4R, TMCO3, GPR156, CDH8, CD79A, TNFRSF13B, HAVCR2, PROSER2, LGALS3BP, C16orf71, MAS1, NLGN3


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 KRT14_TYK2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneKRT14P02533DB01593ZincKeratin, type I cytoskeletal 14small moleculeapproved|investigational
TgeneTYK2P29597DB08895TofacitinibNon-receptor tyrosine-protein kinase TYK2small moleculeapproved|investigational

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RelatedDiseases for KRT14_TYK2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneKRT14C0079295Epidermolysis Bullosa Herpetiformis Dowling-Meara18ORPHANET;UNIPROT
HgeneKRT14C0080333Weber-Cockayne Syndrome10ORPHANET;UNIPROT
HgeneKRT14C0079299Epidermolysis Bullosa Simplex Kobner8ORPHANET;UNIPROT
HgeneKRT14C0007137Squamous cell carcinoma1CTD_human
HgeneKRT14C0007621Neoplastic Cell Transformation1CTD_human
HgeneKRT14C0040411Tongue Neoplasms1CTD_human
HgeneKRT14C0279626Squamous cell carcinoma of esophagus1CTD_human
HgeneKRT14C0343111Naegeli syndrome1CTD_human;ORPHANET
HgeneKRT14C0549567Pigmentation Disorders1CTD_human
HgeneKRT14C1458155Mammary Neoplasms1CTD_human
HgeneKRT14C3715082EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 11ORPHANET;UNIPROT
TgeneTYK2C0003873Rheumatoid Arthritis1CTD_human
TgeneTYK2C0010346Crohn Disease1CTD_human
TgeneTYK2C0023892Biliary cirrhosis1CTD_human
TgeneTYK2C0026769Multiple Sclerosis1CTD_human
TgeneTYK2C0033860Psoriasis1CTD_human
TgeneTYK2C0041696Unipolar Depression1PSYGENET
TgeneTYK2C0236736Cocaine-Related Disorders1CTD_human
TgeneTYK2C0344315Depressed mood1PSYGENET
TgeneTYK2C1269683Major Depressive Disorder1PSYGENET
TgeneTYK2C1456784Paranoia1CTD_human