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Fusion gene ID: 13371 |
FusionGeneSummary for FGF13_CDK14 |
Fusion gene summary |
Fusion gene information | Fusion gene name: FGF13_CDK14 | Fusion gene ID: 13371 | Hgene | Tgene | Gene symbol | FGF13 | CDK14 | Gene ID | 2258 | 5218 |
Gene name | fibroblast growth factor 13 | cyclin dependent kinase 14 | |
Synonyms | FGF-13|FGF2|FHF-2|FHF2 | PFTAIRE1|PFTK1 | |
Cytomap | Xq26.3-q27.1 | 7q21.13 | |
Type of gene | protein-coding | protein-coding | |
Description | fibroblast growth factor 13fibroblast growth factor homologous factor 2 | cyclin-dependent kinase 14PFTAIRE protein kinase 1cell division protein kinase 14serine/threonine-protein kinase PFTAIRE-1 | |
Modification date | 20180519 | 20180523 | |
UniProtAcc | Q92913 | O94921 | |
Ensembl transtripts involved in fusion gene | ENST00000315930, ENST00000305414, ENST00000441825, ENST00000370603, ENST00000541469, | ENST00000380050, ENST00000265741, ENST00000406263, ENST00000436577, ENST00000496279, | |
Fusion gene scores | * DoF score | 6 X 3 X 4=72 | 17 X 14 X 9=2142 |
# samples | 6 | 19 | |
** MAII score | log2(6/72*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(19/2142*10)=-3.49488715641931 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: FGF13 [Title/Abstract] AND CDK14 [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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | FGF13 | GO:0000165 | MAPK cascade | 12244047 |
Tgene | CDK14 | GO:0000086 | G2/M transition of mitotic cell cycle | 20059949 |
Tgene | CDK14 | GO:0060828 | regulation of canonical Wnt signaling pathway | 20059949 |
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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | D16473 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
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. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
intron-intron | ENST00000315930 | ENST00000380050 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000315930 | ENST00000265741 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000315930 | ENST00000406263 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000315930 | ENST00000436577 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000315930 | ENST00000496279 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000305414 | ENST00000380050 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000305414 | ENST00000265741 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000305414 | ENST00000406263 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000305414 | ENST00000436577 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000305414 | ENST00000496279 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000441825 | ENST00000380050 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000441825 | ENST00000265741 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000441825 | ENST00000406263 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000441825 | ENST00000436577 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000441825 | ENST00000496279 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000370603 | ENST00000380050 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000370603 | ENST00000265741 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000370603 | ENST00000406263 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000370603 | ENST00000436577 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000370603 | ENST00000496279 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000541469 | ENST00000380050 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000541469 | ENST00000265741 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000541469 | ENST00000406263 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000541469 | ENST00000436577 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
intron-intron | ENST00000541469 | ENST00000496279 | FGF13 | chrX | 137823303 | - | CDK14 | chr7 | 90681025 | + |
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FusionProtFeatures for FGF13_CDK14 |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
FGF13 | CDK14 |
Microtubule-binding protein which directly binds tubulinand is involved in both polymerization and stabilization ofmicrotubules. Through its action on microtubules, may participateto the refinement of axons by negatively regulating axonal andleading processes branching. Plays a crucial role in neuronpolarization and migration in the cerebral cortex and thehippocampus. {ECO:0000269|PubMed:15282281}. May regulate voltage-gated sodium channels transport andfunction. {ECO:0000269|PubMed:15282281}. May also play a role in MAPK signaling.{ECO:0000269|PubMed:15282281}. |
Retention 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 . * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for FGF13_CDK14 |
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 FGF13_CDK14 |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in . |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for FGF13_CDK14 |
Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for FGF13_CDK14 |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | FGF13 | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Hgene | FGF13 | C0030297 | Pancreatic Neoplasm | 1 | CTD_human |
Tgene | CDK14 | C2239176 | Liver carcinoma | 1 | CTD_human |