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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 35898

FusionGeneSummary for SQSTM1_PKM

check button Fusion gene summary
Fusion gene informationFusion gene name: SQSTM1_PKM
Fusion gene ID: 35898
HgeneTgene
Gene symbol

SQSTM1

PKM

Gene ID

8878

5315

Gene namesequestosome 1pyruvate kinase M1/2
SynonymsA170|DMRV|FTDALS3|NADGP|OSIL|PDB3|ZIP3|p60|p62|p62BCTHBP|HEL-S-30|OIP3|PK3|PKM2|TCB|THBP1
Cytomap

5q35.3

15q23

Type of geneprotein-codingprotein-coding
Descriptionsequestosome-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-bipyruvate kinase PKMOIP-3OPA-interacting protein 3PK, muscle typecytosolic thyroid hormone-binding proteinepididymis secretory protein Li 30p58pyruvate kinase 2/3pyruvate kinase isozymes M1/M2pyruvate kinase muscle isozymepyruvate kinase, muscle
Modification date2018052320180527
UniProtAcc

Q13501

P14618

Ensembl transtripts involved in fusion geneENST00000376929, ENST00000506690, 
ENST00000389805, ENST00000402874, 
ENST00000510187, ENST00000360718, 
ENST00000319622, ENST00000565184, 
ENST00000389093, ENST00000335181, 
ENST00000568883, ENST00000449901, 
ENST00000565154, ENST00000568459, 
Fusion gene scores* DoF score17 X 18 X 7=214220 X 23 X 3=1380
# samples 2124
** MAII scorelog2(21/2142*10)=-3.35049724708413
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(24/1380*10)=-2.52356195605701
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SQSTM1 [Title/Abstract] AND PKM [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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneSQSTM1

GO:0007032

endosome organization

27368102

HgeneSQSTM1

GO:0061635

regulation of protein complex stability

25127057

HgeneSQSTM1

GO:1905719

protein localization to perinuclear region of cytoplasm

27368102

TgenePKM

GO:0012501

programmed cell death

17308100


check button 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 typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BI009652SQSTM1chr5

179251073

-PKMchr15

72494881

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-intronENST00000376929ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000376929ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
intron-intronENST00000506690ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000389805ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000402874ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000510187ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000319622SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000565184SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000389093SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000335181SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000568883SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000449901SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000565154SQSTM1chr5

179251073

-PKMchr15

72494881

-
5CDS-intronENST00000360718ENST00000568459SQSTM1chr5

179251073

-PKMchr15

72494881

-

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FusionProtFeatures for SQSTM1_PKM


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SQSTM1

Q13501

PKM

P14618

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}.

check buttonRetention 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

download page

.

* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for SQSTM1_PKM


check button 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 SQSTM1_PKM


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for SQSTM1_PKM


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgenePKMP14618DB11638ArtenimolPyruvate kinase PKMsmall moleculeapproved|investigational

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RelatedDiseases for SQSTM1_PKM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSQSTM1C4085252PAGET DISEASE OF BONE 312UNIPROT
HgeneSQSTM1C4225326FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 33UNIPROT
HgeneSQSTM1C0002736Amyotrophic Lateral Sclerosis1CTD_human;HPO;ORPHANET
HgeneSQSTM1C0242383Age related macular degeneration1CTD_human
TgenePKMC0027626Neoplasm Invasiveness2CTD_human
TgenePKMC0024667Animal Mammary Neoplasms1CTD_human
TgenePKMC0024668Mammary Neoplasms, Experimental1CTD_human
TgenePKMC0029456Osteoporosis1CTD_human
TgenePKMC2239176Liver carcinoma1CTD_human