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Fusion Protein:MAP1B-SLC27A2 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: MAP1B-SLC27A2 | FusionPDB ID: 51152 | FusionGDB2.0 ID: 51152 | Hgene | Tgene | Gene symbol | MAP1B | SLC27A2 | Gene ID | 4131 | 11001 |
Gene name | microtubule associated protein 1B | solute carrier family 27 member 2 | |
Synonyms | FUTSCH|MAP5|PPP1R102 | ACSVL1|FACVL1|FATP2|HsT17226|VLACS|VLCS|hFACVL1 | |
Cytomap | 5q13.2 | 15q21.2 | |
Type of gene | protein-coding | protein-coding | |
Description | microtubule-associated protein 1Bprotein phosphatase 1, regulatory subunit 102 | very long-chain acyl-CoA synthetaseFATP-2THCA-CoA ligasearachidonate--CoA ligasefatty acid transport protein 2fatty-acid-coenzyme A ligase, very long-chain 1long-chain-fatty-acid--CoA ligasephytanate--CoA ligasesolute carrier family 27 (fatty acid | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | P46821 | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000504183, ENST00000296755, | ENST00000267842, ENST00000380902, ENST00000544960, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 10 X 10 X 5=500 | 5 X 3 X 4=60 |
# samples | 13 | 5 | |
** MAII score | log2(13/500*10)=-1.94341647163363 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/60*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: MAP1B [Title/Abstract] AND SLC27A2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | MAP1B(71411626)-SLC27A2(50489697), # samples:3 | ||
Anticipated loss of major functional domain due to fusion event. | MAP1B-SLC27A2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. MAP1B-SLC27A2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. |
* 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 |
Hgene | MAP1B | GO:0009987 | cellular process | 19567321 |
Tgene | SLC27A2 | GO:0001561 | fatty acid alpha-oxidation | 10198260 |
Tgene | SLC27A2 | GO:0001676 | long-chain fatty acid metabolic process | 22022213 |
Tgene | SLC27A2 | GO:0006635 | fatty acid beta-oxidation | 10198260 |
Tgene | SLC27A2 | GO:0006699 | bile acid biosynthetic process | 11980911 |
Tgene | SLC27A2 | GO:0044539 | long-chain fatty acid import | 22022213 |
Tgene | SLC27A2 | GO:0097089 | methyl-branched fatty acid metabolic process | 10198260 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | PRAD | TCGA-G9-6348-01A | MAP1B | chr5 | 71411626 | - | SLC27A2 | chr15 | 50489697 | + |
ChimerDB4 | PRAD | TCGA-G9-6348-01A | MAP1B | chr5 | 71411626 | + | SLC27A2 | chr15 | 50489697 | + |
ChimerDB4 | PRAD | TCGA-G9-6348 | MAP1B | chr5 | 71411626 | + | SLC27A2 | chr15 | 50489697 | + |
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Fusion ORF Analysis |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000296755 | MAP1B | chr5 | 71411626 | + | ENST00000267842 | SLC27A2 | chr15 | 50489697 | + | 2268 | 584 | 55 | 1968 | 637 |
ENST00000296755 | MAP1B | chr5 | 71411626 | + | ENST00000380902 | SLC27A2 | chr15 | 50489697 | + | 2092 | 584 | 55 | 1809 | 584 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000296755 | ENST00000267842 | MAP1B | chr5 | 71411626 | + | SLC27A2 | chr15 | 50489697 | + | 0.002086761 | 0.9979132 |
ENST00000296755 | ENST00000380902 | MAP1B | chr5 | 71411626 | + | SLC27A2 | chr15 | 50489697 | + | 0.000845381 | 0.99915457 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >51152_51152_1_MAP1B-SLC27A2_MAP1B_chr5_71411626_ENST00000296755_SLC27A2_chr15_50489697_ENST00000267842_length(amino acids)=637AA_BP=176 MPSLHIKAAPPPRPLSLPAPLRRALSAALGEGGGGGGARRQRRGDAGGGAETVPSEIILSPAAVERSGRSETLRRGTAAGRMATVVVEAT EPEPSGSIANPAASTSPSLSHRFLDSKFYLLVVVGEIVTEEHLRRAIGNIELGIRSWDTNLIECNLDQELKLFVSRHSARFSPEVPELQA AVEEILPSLKKDDVSIYYVSRTSNTDGIDSFLDKVDEVSTEPIPESWRSEVTFSTPALYIYTSGTTGLPKAAMITHQRIWYGTGLTFVSG LKADDVIYITLPFYHSAALLIGIHGCIVAGATLALRTKFSASQFWDDCRKYNVTVIQYIGELLRYLCNSPQKPNDRDHKVRLALGNGLRG DVWRQFVKRFGDICIYEFYAATEGNIGFMNYARKVGAVGRVNYLQKKIITYDLIKYDVEKDEPVRDENGYCVRVPKGEVGLLVCKITQLT PFNGYAGAKAQTEKKKLRDVFKKGDLYFNSGDLLMVDHENFIYFHDRVGDTFRWKGENVATTEVADTVGLVDFVQEVNVYGVHVPDHEGR IGMASIKMKENHEFDGKKLFQHIADYLPSYARPRFLRIQDTIEITGTFKHRKMTLVEEGFNPAVIKDALYFLDDTAKMYVPMTEDIYNAI -------------------------------------------------------------- >51152_51152_2_MAP1B-SLC27A2_MAP1B_chr5_71411626_ENST00000296755_SLC27A2_chr15_50489697_ENST00000380902_length(amino acids)=584AA_BP=176 MPSLHIKAAPPPRPLSLPAPLRRALSAALGEGGGGGGARRQRRGDAGGGAETVPSEIILSPAAVERSGRSETLRRGTAAGRMATVVVEAT EPEPSGSIANPAASTSPSLSHRFLDSKFYLLVVVGEIVTEEHLRRAIGNIELGIRSWDTNLIECNLDQELKLFVSRHSARFSPEVPELQA AVEEILPSLKKDDVSIYYVSRTSNTDGIDSFLDKVDEVSTEPIPESWRSEVTFSTPALYIYTSGTTGATLALRTKFSASQFWDDCRKYNV TVIQYIGELLRYLCNSPQKPNDRDHKVRLALGNGLRGDVWRQFVKRFGDICIYEFYAATEGNIGFMNYARKVGAVGRVNYLQKKIITYDL IKYDVEKDEPVRDENGYCVRVPKGEVGLLVCKITQLTPFNGYAGAKAQTEKKKLRDVFKKGDLYFNSGDLLMVDHENFIYFHDRVGDTFR WKGENVATTEVADTVGLVDFVQEVNVYGVHVPDHEGRIGMASIKMKENHEFDGKKLFQHIADYLPSYARPRFLRIQDTIEITGTFKHRKM -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr5:71411626/chr15:50489697) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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Hgene | Tgene |
MAP1B | . |
FUNCTION: Facilitates tyrosination of alpha-tubulin in neuronal microtubules (By similarity). Phosphorylated MAP1B may play a role in the cytoskeletal changes that accompany neurite extension. Possibly MAP1B binds to at least two tubulin subunits in the polymer, and this bridging of subunits might be involved in nucleating microtubule polymerization and in stabilizing microtubules. Acts as a positive cofactor in DAPK1-mediated autophagic vesicle formation and membrane blebbing. {ECO:0000250, ECO:0000269|PubMed:18195017}. | FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. |
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- 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 |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 222_233 | 159.33333333333334 | 621.0 | Nucleotide binding | AMP | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 222_233 | 159.33333333333334 | 568.0 | Nucleotide binding | AMP | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 283_620 | 159.33333333333334 | 621.0 | Topological domain | Cytoplasmic | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 283_620 | 159.33333333333334 | 568.0 | Topological domain | Cytoplasmic | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 262_282 | 159.33333333333334 | 621.0 | Transmembrane | Helical | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 262_282 | 159.33333333333334 | 568.0 | Transmembrane | Helical |
- 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 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 589_790 | 95.33333333333333 | 2469.0 | Compositional bias | Note=Lys-rich (highly basic%2C contains many KKEE and KKEI/V repeats) |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1878_1894 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 1 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1895_1911 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 2 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1912_1928 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 3 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1929_1945 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 4 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1946_1962 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 5 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1963_1979 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 6 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 1997_2013 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 7 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 2014_2030 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 8 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 2031_2047 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 9 |
Hgene | MAP1B | chr5:71411626 | chr15:50489697 | ENST00000296755 | + | 2 | 7 | 2048_2064 | 95.33333333333333 | 2469.0 | Repeat | Note=MAP1B 10 |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 128_261 | 159.33333333333334 | 621.0 | Topological domain | Lumenal | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 1_4 | 159.33333333333334 | 621.0 | Topological domain | Lumenal | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 28_106 | 159.33333333333334 | 621.0 | Topological domain | Cytoplasmic | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 128_261 | 159.33333333333334 | 568.0 | Topological domain | Lumenal | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 1_4 | 159.33333333333334 | 568.0 | Topological domain | Lumenal | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 28_106 | 159.33333333333334 | 568.0 | Topological domain | Cytoplasmic | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 107_127 | 159.33333333333334 | 621.0 | Transmembrane | Helical | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000267842 | 0 | 10 | 5_27 | 159.33333333333334 | 621.0 | Transmembrane | Helical | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 107_127 | 159.33333333333334 | 568.0 | Transmembrane | Helical | |
Tgene | SLC27A2 | chr5:71411626 | chr15:50489697 | ENST00000380902 | 0 | 9 | 5_27 | 159.33333333333334 | 568.0 | Transmembrane | Helical |
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Fusion Protein Structures |
![]() * Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format. |
Fusion protein PDB link (fusion AA seq ID in FusionPDB) | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | AA seq | Len(AA seq) |
PDB file >>>1337_MAP1B_71411626_SLC27A2_50489697_1337_MAP1B_71411626_SLC27A2_50489697_ranked_0.pdb | MAP1B | 71411626 | 71411626 | ENST00000380902 | SLC27A2 | chr15 | 50489697 | + | MPSLHIKAAPPPRPLSLPAPLRRALSAALGEGGGGGGARRQRRGDAGGGAETVPSEIILSPAAVERSGRSETLRRGTAAGRMATVVVEAT EPEPSGSIANPAASTSPSLSHRFLDSKFYLLVVVGEIVTEEHLRRAIGNIELGIRSWDTNLIECNLDQELKLFVSRHSARFSPEVPELQA AVEEILPSLKKDDVSIYYVSRTSNTDGIDSFLDKVDEVSTEPIPESWRSEVTFSTPALYIYTSGTTGLPKAAMITHQRIWYGTGLTFVSG LKADDVIYITLPFYHSAALLIGIHGCIVAGATLALRTKFSASQFWDDCRKYNVTVIQYIGELLRYLCNSPQKPNDRDHKVRLALGNGLRG DVWRQFVKRFGDICIYEFYAATEGNIGFMNYARKVGAVGRVNYLQKKIITYDLIKYDVEKDEPVRDENGYCVRVPKGEVGLLVCKITQLT PFNGYAGAKAQTEKKKLRDVFKKGDLYFNSGDLLMVDHENFIYFHDRVGDTFRWKGENVATTEVADTVGLVDFVQEVNVYGVHVPDHEGR IGMASIKMKENHEFDGKKLFQHIADYLPSYARPRFLRIQDTIEITGTFKHRKMTLVEEGFNPAVIKDALYFLDDTAKMYVPMTEDIYNAI | 637 |
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pLDDT score distribution |
![]() * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
MAP1B_pLDDT.png![]() |
SLC27A2_pLDDT.png![]() |
![]() * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
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Ramachandran Plot of Fusion Protein Structure |
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Fusion AA seq ID in FusionPDB and their Ramachandran plots |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
MAP1B | |
SLC27A2 |
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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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Related Drugs to MAP1B-SLC27A2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to MAP1B-SLC27A2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |