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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: 3410

FusionGeneSummary for ATP5H_SPG11

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP5H_SPG11
Fusion gene ID: 3410
HgeneTgene
Gene symbol

ATP5H

SPG11

Gene ID

80208

Gene nameSPG11, spatacsin vesicle trafficking associated
SynonymsALS5|CMT2X|KIAA1840
Cytomap

15q21.1

Type of geneprotein-coding
Descriptionspatacsincolorectal carcinoma-associated proteinspastic paraplegia 11 (autosomal recessive)spastic paraplegia 11 protein
Modification date20180519
UniProtAcc

O75947

Q96JI7

Ensembl transtripts involved in fusion geneENST00000301587, ENST00000344546, 
ENST00000261866, ENST00000535302, 
ENST00000427534, ENST00000558319, 
ENST00000558253, ENST00000559193, 
Fusion gene scores* DoF score4 X 2 X 4=322 X 2 X 2=8
# samples 42
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: ATP5H [Title/Abstract] AND SPG11 [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

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
TCGALDTHCATCGA-DJ-A2PN-01AATP5Hchr17

73038276

-SPG11chr15

44865943

-
* 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-shiftENST00000301587ENST00000261866ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000301587ENST00000535302ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000301587ENST00000427534ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000301587ENST00000558319ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000301587ENST00000558253ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000301587ENST00000559193ATP5Hchr17

73038276

-SPG11chr15

44865943

-
Frame-shiftENST00000344546ENST00000261866ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000344546ENST00000535302ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000344546ENST00000427534ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000344546ENST00000558319ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000344546ENST00000558253ATP5Hchr17

73038276

-SPG11chr15

44865943

-
5CDS-intronENST00000344546ENST00000559193ATP5Hchr17

73038276

-SPG11chr15

44865943

-

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FusionProtFeatures for ATP5H_SPG11


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ATP5H

O75947

SPG11

Q96JI7

Mitochondrial membrane ATP synthase (F(1)F(0) ATPsynthase or Complex V) produces ATP from ADP in the presence of aproton gradient across the membrane which is generated by electrontransport complexes of the respiratory chain. F-type ATPasesconsist of two structural domains, F(1) - containing theextramembraneous catalytic core, and F(0) - containing themembrane proton channel, linked together by a central stalk and aperipheral stalk. During catalysis, ATP synthesis in the catalyticdomain of F(1) is coupled via a rotary mechanism of the centralstalk subunits to proton translocation. Part of the complex F(0)domain and the peripheric stalk, which acts as a stator to holdthe catalytic alpha(3)beta(3) subcomplex and subunit a/ATP6 staticrelative to the rotary elements.

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 ATP5H_SPG11


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 ATP5H_SPG11


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
ATP5HICT1, APP, ATP5O, NDUFA12, UQCRQ, STOML2, UBL4A, FBXW4, CCDC8, BLK, ATP5F1, ATP5D, ATP5A1, ATP5B, ATP5L, OGDH, RAB1A, VDAC3, ATP5I, CHCHD2, CISD1, CYC1, PDIA3, RER1, MED4, CENPA, TSNAX, TM9SF4, TFG, TMEM63B, FAM134A, ACKR3, USF1, PTPMT1, COQ9, NDUFA4, C15orf48, CISD3, C17orf89, PAK7, ADCK1, CHCHD10, APOOL, FAM136A, ADCK4, NDUFS3, C7orf55, OCIAD1, C2orf47, PTPN5, DKK3, ZFYVE27, TACR1, P2RY12, UBC, STOM, COX15, PDHA1, SDHA, VDAC1SPG11SERTAD3, AP5M1, LINC01587, CRYL1, VIPR2


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 ATP5H_SPG11


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 ATP5H_SPG11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSPG11C1858479Spastic paraplegia 11, autosomal recessive1CTD_human;ORPHANET;UNIPROT