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Fusion gene ID: 13123 |
FusionGeneSummary for FBXL4_APBA2 |
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Fusion gene information | Fusion gene name: FBXL4_APBA2 | Fusion gene ID: 13123 | Hgene | Tgene | Gene symbol | FBXL4 | APBA2 | Gene ID | 26235 | 321 |
Gene name | F-box and leucine rich repeat protein 4 | amyloid beta precursor protein binding family A member 2 | |
Synonyms | FBL4|FBL5|MTDPS13 | D15S1518E|HsT16821|LIN-10|MGC:14091|MINT2|X11-BETA|X11L | |
Cytomap | 6q16.1-q16.2 | 15q13.1 | |
Type of gene | protein-coding | protein-coding | |
Description | F-box/LRR-repeat protein 4 | amyloid-beta A4 precursor protein-binding family A member 2X11-like proteinadapter protein X11betaamyloid beta (A4) precursor protein-binding, family A, member 2 (X11-like)mint-2neuron-specific X11L proteinneuronal munc18-1-interacting protein 2pho | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q9UKA2 | Q99767 | |
Ensembl transtripts involved in fusion gene | ENST00000369244, ENST00000229971, | ENST00000561069, ENST00000558402, ENST00000558330, ENST00000411764, ENST00000558259, | |
Fusion gene scores | * DoF score | 5 X 5 X 2=50 | 1 X 1 X 1=1 |
# samples | 5 | 1 | |
** MAII score | log2(5/50*10)=0 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: FBXL4 [Title/Abstract] AND APBA2 [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
![]() (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 | BF885322 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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-3CDS | ENST00000369244 | ENST00000561069 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000369244 | ENST00000558402 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000369244 | ENST00000558330 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000369244 | ENST00000411764 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000369244 | ENST00000558259 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000229971 | ENST00000561069 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000229971 | ENST00000558402 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000229971 | ENST00000558330 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000229971 | ENST00000411764 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
intron-3CDS | ENST00000229971 | ENST00000558259 | FBXL4 | chr6 | 99347218 | + | APBA2 | chr15 | 29368266 | + |
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FusionProtFeatures for FBXL4_APBA2 |
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Hgene | Tgene |
FBXL4 | APBA2 |
Putative function in synaptic vesicle exocytosis bybinding to STXBP1, an essential component of the synaptic vesicleexocytotic machinery. May modulate processing of the amyloid-betaprecursor protein (APP) and hence formation of APP-beta. |
![]() * 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 FBXL4_APBA2 |
![]() (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 FBXL4_APBA2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for FBXL4_APBA2 |
![]() (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 FBXL4_APBA2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | FBXL4 | C3809592 | MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE) | 2 | ORPHANET;UNIPROT |
Tgene | APBA2 | C0036341 | Schizophrenia | 1 | PSYGENET |