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Fusion gene ID: 35888 |
FusionGeneSummary for SQSTM1_CPB1 |
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Fusion gene information | Fusion gene name: SQSTM1_CPB1 | Fusion gene ID: 35888 | Hgene | Tgene | Gene symbol | SQSTM1 | CPB1 | Gene ID | 8878 | 1360 |
Gene name | sequestosome 1 | carboxypeptidase B1 | |
Synonyms | A170|DMRV|FTDALS3|NADGP|OSIL|PDB3|ZIP3|p60|p62|p62B | CPB|PASP|PCPB | |
Cytomap | 5q35.3 | 3q24 | |
Type of gene | protein-coding | protein-coding | |
Description | sequestosome-1EBI3-associated protein of 60 kDaEBI3-associated protein p60EBIAPoxidative stress induced likephosphotyrosine independent ligand for the Lck SH2 domain p62phosphotyrosine-independent ligand for the Lck SH2 domain of 62 kDaubiquitin-bi | carboxypeptidase Bcarboxypeptidase B1 (tissue)pancreas-specific proteinpancreatic carboxypeptidase Bprocarboxypeptidase Bprotaminasetissue carboxypeptidase B | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q13501 | P15086 | |
Ensembl transtripts involved in fusion gene | ENST00000376929, ENST00000506690, ENST00000389805, ENST00000402874, ENST00000510187, ENST00000360718, | ENST00000491148, ENST00000282957, ENST00000498639, | |
Fusion gene scores | * DoF score | 17 X 18 X 7=2142 | 21 X 24 X 3=1512 |
# samples | 21 | 19 | |
** MAII score | log2(21/2142*10)=-3.35049724708413 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(19/1512*10)=-2.99238681589013 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: SQSTM1 [Title/Abstract] AND CPB1 [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 |
Hgene | SQSTM1 | GO:0007032 | endosome organization | 27368102 |
Hgene | SQSTM1 | GO:0061635 | regulation of protein complex stability | 25127057 |
Hgene | SQSTM1 | GO:1905719 | protein localization to perinuclear region of cytoplasm | 27368102 |
![]() (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 |
TCGA | LD | BRCA | TCGA-A8-A091-01A | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
* 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 |
3UTR-3CDS | ENST00000376929 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000376929 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-intron | ENST00000376929 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
intron-3CDS | ENST00000506690 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
intron-3CDS | ENST00000506690 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
intron-intron | ENST00000506690 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000389805 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000389805 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-intron | ENST00000389805 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000402874 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000402874 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-intron | ENST00000402874 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000510187 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000510187 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-intron | ENST00000510187 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000360718 | ENST00000491148 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-3CDS | ENST00000360718 | ENST00000282957 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
3UTR-intron | ENST00000360718 | ENST00000498639 | SQSTM1 | chr5 | 179263664 | + | CPB1 | chr3 | 148558473 | + |
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FusionProtFeatures for SQSTM1_CPB1 |
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Hgene | Tgene |
SQSTM1 | CPB1 |
Autophagy receptor required for selective macroautophagy(aggrephagy). Functions as a bridge between polyubiquitinatedcargo and autophagosomes. Interacts directly with both the cargoto become degraded and an autophagy modifier of the MAP1 LC3family (PubMed:16286508, PubMed:20168092, PubMed:24128730,PubMed:28404643, PubMed:22622177). Along with WDFY3, involved inthe formation and autophagic degradation of cytoplasmic ubiquitin-containing inclusions (p62 bodies, ALIS/aggresome-like inducedstructures). Along with WDFY3, required to recruit ubiquitinatedproteins to PML bodies in the nucleus (PubMed:24128730,PubMed:20168092). May regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1. May play arole in titin/TTN downstream signaling in muscle cells. Mayregulate signaling cascades through ubiquitination. Adapter thatmediates the interaction between TRAF6 and CYLD (By similarity).May be involved in cell differentiation, apoptosis, immuneresponse and regulation of K(+) channels. Involved in endosomeorganization by retaining vesicles in the perinuclear cloud:following ubiquitination by RNF26, attracts specific vesicle-associated adapters, forming a molecular bridge that restrainscognate vesicles in the perinuclear region and organizes theendosomal pathway for efficient cargo transport (PubMed:27368102).{ECO:0000250|UniProtKB:O08623, ECO:0000250|UniProtKB:Q64337,ECO:0000269|PubMed:10356400, ECO:0000269|PubMed:10747026,ECO:0000269|PubMed:11244088, ECO:0000269|PubMed:12471037,ECO:0000269|PubMed:15340068, ECO:0000269|PubMed:15802564,ECO:0000269|PubMed:15911346, ECO:0000269|PubMed:15953362,ECO:0000269|PubMed:16079148, ECO:0000269|PubMed:16286508,ECO:0000269|PubMed:19931284, ECO:0000269|PubMed:20168092,ECO:0000269|PubMed:22622177, ECO:0000269|PubMed:24128730,ECO:0000269|PubMed:27368102, ECO:0000269|PubMed:28404643}. |
![]() * 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 SQSTM1_CPB1 |
![]() (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 SQSTM1_CPB1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
SQSTM1 | GABARAPL2, RAD23A, GABARAPL1, SQSTM1, LINC00341, MAP1LC3B, TRAF6, PRKCZ, IRAK1, PRKCI, NTRK1, RIPK1, NTRK2, NTRK3, LCK, MAP1LC3A, KEAP1, GABARAP, C10orf2, ABHD10, CEP78, DIP2B, BLOC1S5, EMILIN3, NSUN4, OSBPL8, INA, NIPSNAP1, GBAS, LLGL1, HADHA, GPC4, HADHB, CTNND1, ASPH, ENPP1, TRMT61B, GLG1, MRPL38, NEFM, GTF3C3, SRRM2, MYD88, MYC, MAP3K3, MAP2K5, IRF8, TRIM21, CYLD, CALM1, BNIP1, NFE2L2, CUL3, PIK3CA, PPHLN1, BPTF, UBC, DAZAP2, CDC37, TRIM13, CASP8, PCK1, STAT5A, PDE4A, MAPT, ATG4B, CHMP2B, TARDBP, CUL1, CUL2, HDAC6, ATG7, FUS, CSNK2A1, ZFAND5, TUBA1A, WDFY3, BAG3, NBR1, SNCA, TRIM63, TRIM55, TTN, RARA, PSMC2, PSMD4, MAP1LC3C, TRIM50, ARHGEF28, TGM2, PAWR, RPTOR, MTOR, AKT1S1, MLST8, RPS6KB1, RRAGC, RRAGB, CDK9, SPRED2, TRIM5, AJUBA, LIMD1, MAPK14, PARP10, TNFRSF10A, HTT, HNRNPA2B1, SDHA, CAV1, BID, FAS, SESN2, SESN1, MALT1, IKBKG, FHOD3, NOD2, SYNPO2, PYCARD, MLH1, PARK2, BCL2, PAN2, NPM1, MBP, YWHAZ, STXBP1, FKBP4, MEIS2, TKT, HSPA4, RELN, CAMK2A, ULK2, NCOR1, NGFR, CALCOCO2, CDK1, CCNB1, PRKCD, MAPK1, SMAD3, EEF1D, RPL37, GEMIN4, DVL2, CHAF1A, TP53, CASP9, HIF1A, PSMD12, PSMD3, FLNB, PSMD10, TXNL1, TNK2, LGALS3, EDEM1, CFTR, CSNK2A2, DCP2, EGLN3, EPAS1, ULK1, TOLLIP, OPTN, ATXN3, STUB1, ISG15, MOV10, NXF1, CUL7, PIK3R1, PIK3R2, AGAP1, INSR, TBK1, CRHBP, SCCPDH, DNAI1, DNAI2, TP53INP1, LLGL2, HSPB1, IFI16, KIAA0753, MED4, CEP135, CNTRL, SASS6, TMEM17, XPO1, CD44, KIF5B, PML, ENC1, SKI, TRIB3, RBM45, MAPK13, CHDH, EPDR1, GAS6, NDUFS2, NDUFS3, GFM2, NDUFA5, CD48, LDHA, RCN2, TRAF1, GBP2, KLHL3, EPM2A, RAD54L2, HSPA5, GRIA1, UBXN1, PEX5, BCL10, ATG5, CSNK1A1, VANGL2, SERPINA1, LRRK2, VHL, TCEB2, TCEB1, RNF166, NOTCH1, RETN, KERA, INSL5, TMX1, VWCE, CD96, HTR3A, RNF26, INO80B, DLST, TRIM25, PLIN1, TES, WDR81, PSMA6, TRIM23 | CPB1 |
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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 SQSTM1_CPB1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | CPB1 | P15086 | DB04272 | Citric Acid | Carboxypeptidase B | small molecule | approved|nutraceutical|vet_approved |
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RelatedDiseases for SQSTM1_CPB1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | SQSTM1 | C4085252 | PAGET DISEASE OF BONE 3 | 12 | UNIPROT |
Hgene | SQSTM1 | C4225326 | FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3 | 3 | UNIPROT |
Hgene | SQSTM1 | C0002736 | Amyotrophic Lateral Sclerosis | 1 | CTD_human;HPO;ORPHANET |
Hgene | SQSTM1 | C0242383 | Age related macular degeneration | 1 | CTD_human |