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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: 16308

FusionGeneSummary for HK1_SUPV3L1

check button Fusion gene summary
Fusion gene informationFusion gene name: HK1_SUPV3L1
Fusion gene ID: 16308
HgeneTgene
Gene symbol

HK1

SUPV3L1

Gene ID

255061

6832

Gene nametachykinin 4Suv3 like RNA helicase
SynonymsEK|HK-1|HK1|PPT-CSUV3
Cytomap

17q21.33

10q22.1

Type of geneprotein-codingprotein-coding
Descriptiontachykinin-4endokininpreprotachykinin-Ctachykinin 4 (hemokinin)ATP-dependent RNA helicase SUPV3L1, mitochondrialSUV3-like helicaseSUV3-like protein 1suppressor of var1, 3-like 1suppressor of var1, 3-like 1(SUV3)
Modification date2018052320180523
UniProtAcc

P19367

Q8IYB8

Ensembl transtripts involved in fusion geneENST00000360289, ENST00000448642, 
ENST00000404387, ENST00000298649, 
ENST00000359426, ENST00000494253, 
ENST00000359655, ENST00000483572, 
Fusion gene scores* DoF score7 X 10 X 3=2104 X 4 X 3=48
# samples 104
** MAII scorelog2(10/210*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HK1 [Title/Abstract] AND SUPV3L1 [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
HgeneHK1

GO:1902093

positive regulation of flagellated sperm motility

17437961

TgeneSUPV3L1

GO:0000962

positive regulation of mitochondrial RNA catabolic process

19509288


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
TCGALDBRCATCGA-AR-A256-01AHK1chr10

71103745

+SUPV3L1chr10

70967549

+
* 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
Frame-shiftENST00000360289ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
5CDS-intronENST00000360289ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+
Frame-shiftENST00000448642ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
5CDS-intronENST00000448642ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+
Frame-shiftENST00000404387ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
5CDS-intronENST00000404387ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+
Frame-shiftENST00000298649ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
5CDS-intronENST00000298649ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+
Frame-shiftENST00000359426ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
5CDS-intronENST00000359426ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+
3UTR-3CDSENST00000494253ENST00000359655HK1chr10

71103745

+SUPV3L1chr10

70967549

+
3UTR-intronENST00000494253ENST00000483572HK1chr10

71103745

+SUPV3L1chr10

70967549

+

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FusionProtFeatures for HK1_SUPV3L1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HK1

P19367

SUPV3L1

Q8IYB8

Major helicase player in mitochondrial RNA metabolism.Component of the mitochondrial degradosome (mtEXO) complex, thatdegrades 3' overhang double-stranded RNA with a 3'-to-5'directionality in an ATP-dependent manner. ATPase and ATP-dependent multisubstrate helicase, able to unwind double-stranded(ds) DNA and RNA, and RNA/DNA heteroduplexes in the 5'-to-3'direction. Plays a role in the RNA surveillance system inmitochondria; regulates the stability of mature mRNAs, the removalof aberrantly formed mRNAs and the rapid degradation of non codingprocessing intermediates. Also implicated in recombination andchromatin maintenance pathways. May protect cells from apoptosis.Associates with mitochondrial DNA. {ECO:0000269|PubMed:12466530,ECO:0000269|PubMed:15096047, ECO:0000269|PubMed:17352692,ECO:0000269|PubMed:17961633, ECO:0000269|PubMed:18678873,ECO:0000269|PubMed:19509288, ECO:0000269|PubMed:19864255}.

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 HK1_SUPV3L1


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 HK1_SUPV3L1


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
HK1ENO2, ATG101, GBAS, ICT1, SIRT7, CDK2, AKT1, PARK2, APP, LIG4, ATF2, VDAC1, AHCY, ASL, CAPN2, GTF3C4, ARFGAP1, FKBP9, HEXA, HEXB, PDCD10, PROSC, RARS, SGTA, WDR61, NSFL1C, PARP6, PCNA, PLAA, TUBB2A, TUFM, TWF2, UBA5, UBXN1, EGFR, STAU1, ASPDH, HYOU1, NTRK1, CNTRL, FBF1, NPHP1, U2AF2, CDC73, HKDC1, HK2, CAV1, SNCA, ASPSCR1, HK3, TESSUPV3L1ICT1, ELAVL1, CUL3, LZTS2, ZMAT3, HNRNPDL, HNRNPA1, NTRK1, CDC5L, PNPT1, ELAVL2, MRPS11, RBM3, MRPS34, USP9X, RBM42, HNRNPF, ZNF703, WASF3, BHLHA15


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 HK1_SUPV3L1


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

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RelatedDiseases for HK1_SUPV3L1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHK1C3150343HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY2CTD_human;ORPHANET;UNIPROT
HgeneHK1C0011853Diabetes Mellitus, Experimental1CTD_human
HgeneHK1C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneHK1C0036341Schizophrenia1PSYGENET
HgeneHK1C0151744Myocardial Ischemia1CTD_human
TgeneSUPV3L1C0002170Alopecia1CTD_human
TgeneSUPV3L1C0020757Ichthyoses1CTD_human
TgeneSUPV3L1C0037268Skin Abnormalities1CTD_human
TgeneSUPV3L1C0872084Sarcopenia1CTD_human