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Fusion gene ID: 12407 |
FusionGeneSummary for FAAH_FAAH |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: FAAH_FAAH | Fusion gene ID: 12407 | Hgene | Tgene | Gene symbol | FAAH | FAAH | Gene ID | 79152 | 79152 |
| Gene name | fatty acid 2-hydroxylase | fatty acid 2-hydroxylase | |
| Synonyms | FAAH|FAH1|FAXDC1|SCS7|SPG35 | FAAH|FAH1|FAXDC1|SCS7|SPG35 | |
| Cytomap | 16q23.1 | 16q23.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | fatty acid 2-hydroxylasefatty acid alpha-hydroxylasefatty acid hydroxylase domain containing 1spastic paraplegia 35 (autosomal recessive) | fatty acid 2-hydroxylasefatty acid alpha-hydroxylasefatty acid hydroxylase domain containing 1spastic paraplegia 35 (autosomal recessive) | |
| Modification date | 20180523 | 20180523 | |
| UniProtAcc | O00519 | O00519 | |
| Ensembl transtripts involved in fusion gene | ENST00000243167, ENST00000493735, | ENST00000243167, ENST00000493735, | |
| Fusion gene scores | * DoF score | 2 X 2 X 2=8 | 2 X 2 X 2=8 |
| # samples | 2 | 2 | |
| ** MAII score | log2(2/8*10)=1.32192809488736 | log2(2/8*10)=1.32192809488736 | |
| Context | PubMed: FAAH [Title/Abstract] AND FAAH [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 |
| 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 | BF766834 | FAAH | chr1 | 46879292 | + | FAAH | chr1 | 46879145 | - |
| * 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 |
| 3UTR-3CDS | ENST00000243167 | ENST00000243167 | FAAH | chr1 | 46879292 | + | FAAH | chr1 | 46879145 | - |
| 3UTR-intron | ENST00000243167 | ENST00000493735 | FAAH | chr1 | 46879292 | + | FAAH | chr1 | 46879145 | - |
| intron-3CDS | ENST00000493735 | ENST00000243167 | FAAH | chr1 | 46879292 | + | FAAH | chr1 | 46879145 | - |
| intron-intron | ENST00000493735 | ENST00000493735 | FAAH | chr1 | 46879292 | + | FAAH | chr1 | 46879145 | - |
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FusionProtFeatures for FAAH_FAAH |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| FAAH | FAAH |
| Degrades bioactive fatty acid amides like oleamide, theendogenous cannabinoid, anandamide and myristic amide to theircorresponding acids, thereby serving to terminate the signalingfunctions of these molecules. Hydrolyzes polyunsaturated substrateanandamide preferentially as compared to monounsaturatedsubstrates. {ECO:0000269|PubMed:17015445}. | Degrades bioactive fatty acid amides like oleamide, theendogenous cannabinoid, anandamide and myristic amide to theircorresponding acids, thereby serving to terminate the signalingfunctions of these molecules. Hydrolyzes polyunsaturated substrateanandamide preferentially as compared to monounsaturatedsubstrates. {ECO:0000269|PubMed:17015445}. |
| 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 FAAH_FAAH |
| 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 FAAH_FAAH |
| 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 FAAH_FAAH |
| 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 |
| Hgene | FAAH | O00519 | DB00316 | Acetaminophen | Fatty-acid amide hydrolase 1 | small molecule | approved |
| Hgene | FAAH | O00519 | DB00599 | Thiopental | Fatty-acid amide hydrolase 1 | small molecule | approved|vet_approved |
| Tgene | FAAH | O00519 | DB00316 | Acetaminophen | Fatty-acid amide hydrolase 1 | small molecule | approved |
| Tgene | FAAH | O00519 | DB00599 | Thiopental | Fatty-acid amide hydrolase 1 | small molecule | approved|vet_approved |
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RelatedDiseases for FAAH_FAAH |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | FAAH | C0024809 | Marijuana Abuse | 3 | PSYGENET |
| Hgene | FAAH | C0028754 | Obesity | 2 | CTD_human |
| Hgene | FAAH | C0038587 | Substance Withdrawal Syndrome | 2 | CTD_human |
| Hgene | FAAH | C0236969 | Substance-Related Disorders | 2 | CTD_human |
| Hgene | FAAH | C0006870 | Cannabis Dependence | 1 | PSYGENET |
| Hgene | FAAH | C0020179 | Huntington Disease | 1 | CTD_human |
| Hgene | FAAH | C0032962 | Pregnancy Complications | 1 | CTD_human |
| Hgene | FAAH | C0033975 | Psychotic Disorders | 1 | PSYGENET |
| Hgene | FAAH | C0036341 | Schizophrenia | 1 | PSYGENET |
| Hgene | FAAH | C0036572 | Seizures | 1 | CTD_human |
| Hgene | FAAH | C0041696 | Unipolar Depression | 1 | PSYGENET |
| Hgene | FAAH | C0349204 | Nonorganic psychosis | 1 | PSYGENET |
| Hgene | FAAH | C0525045 | Mood Disorders | 1 | PSYGENET |
| Hgene | FAAH | C1269683 | Major Depressive Disorder | 1 | PSYGENET |
| Tgene | FAAH | C0024809 | Marijuana Abuse | 3 | PSYGENET |
| Tgene | FAAH | C0028754 | Obesity | 2 | CTD_human |
| Tgene | FAAH | C0038587 | Substance Withdrawal Syndrome | 2 | CTD_human |
| Tgene | FAAH | C0236969 | Substance-Related Disorders | 2 | CTD_human |
| Tgene | FAAH | C0006870 | Cannabis Dependence | 1 | PSYGENET |
| Tgene | FAAH | C0020179 | Huntington Disease | 1 | CTD_human |
| Tgene | FAAH | C0032962 | Pregnancy Complications | 1 | CTD_human |
| Tgene | FAAH | C0033975 | Psychotic Disorders | 1 | PSYGENET |
| Tgene | FAAH | C0036341 | Schizophrenia | 1 | PSYGENET |
| Tgene | FAAH | C0036572 | Seizures | 1 | CTD_human |
| Tgene | FAAH | C0041696 | Unipolar Depression | 1 | PSYGENET |
| Tgene | FAAH | C0349204 | Nonorganic psychosis | 1 | PSYGENET |
| Tgene | FAAH | C0525045 | Mood Disorders | 1 | PSYGENET |
| Tgene | FAAH | C1269683 | Major Depressive Disorder | 1 | PSYGENET |
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