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Fusion gene ID: 32634 |
FusionGeneSummary for SAR1B_KLF12 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: SAR1B_KLF12 | Fusion gene ID: 32634 | Hgene | Tgene | Gene symbol | SAR1B | KLF12 | Gene ID | 51128 | 11278 |
| Gene name | secretion associated Ras related GTPase 1B | Kruppel like factor 12 | |
| Synonyms | ANDD|CMRD|GTBPB|SARA2 | AP-2rep|AP2REP|HSPC122 | |
| Cytomap | 5q31.1 | 13q22.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | GTP-binding protein SAR1b2310075M17RikGTP-binding protein BGTP-binding protein SaraSAR1 homolog BSAR1a gene homolog 2 | Krueppel-like factor 12AP-2 repressorAP-2rep transcription factorKLF12 zinc finger transcriptional repressortranscriptional repressor AP-2rep | |
| Modification date | 20180523 | 20180523 | |
| UniProtAcc | Q9Y6B6 | Q9Y4X4 | |
| Ensembl transtripts involved in fusion gene | ENST00000402673, ENST00000507419, ENST00000439578, ENST00000502539, ENST00000509937, ENST00000504242, | ENST00000377669, ENST00000377666, ENST00000472022, | |
| Fusion gene scores | * DoF score | 2 X 2 X 1=4 | 9 X 10 X 4=360 |
| # samples | 2 | 11 | |
| ** MAII score | log2(2/4*10)=2.32192809488736 | log2(11/360*10)=-1.71049338280502 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: SAR1B [Title/Abstract] AND KLF12 [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 |
| Tgene | KLF12 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 16615998 |
| 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 | CN421624 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| * 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-3UTR | ENST00000402673 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000402673 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000402673 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-3UTR | ENST00000507419 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000507419 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000507419 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-3UTR | ENST00000439578 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000439578 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000439578 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-3UTR | ENST00000502539 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000502539 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000502539 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-3UTR | ENST00000509937 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000509937 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000509937 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-3UTR | ENST00000504242 | ENST00000377669 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000504242 | ENST00000377666 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
| intron-intron | ENST00000504242 | ENST00000472022 | SAR1B | chr5 | 133938876 | - | KLF12 | chr13 | 74263784 | - |
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FusionProtFeatures for SAR1B_KLF12 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| SAR1B | KLF12 |
| Involved in transport from the endoplasmic reticulum tothe Golgi apparatus. Activated by the guanine nucleotide exchangefactor PREB. Involved in the selection of the protein cargo andthe assembly of the COPII coat complex. | Confers strong transcriptional repression to the AP-2-alpha gene. Binds to a regulatory element (A32) in the AP-2-alphagene promoter. |
| 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 SAR1B_KLF12 |
| 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 SAR1B_KLF12 |
| 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 SAR1B_KLF12 |
| 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 SAR1B_KLF12 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | SAR1B | C0795956 | Chylomicron retention disease | 2 | CTD_human;ORPHANET;UNIPROT |
| Tgene | KLF12 | C0036341 | Schizophrenia | 1 | CTD_human |
| Tgene | KLF12 | C0236969 | Substance-Related Disorders | 1 | CTD_human |
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