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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: 25644

FusionGeneSummary for OXCT1_TMEM17

check button Fusion gene summary
Fusion gene informationFusion gene name: OXCT1_TMEM17
Fusion gene ID: 25644
HgeneTgene
Gene symbol

OXCT1

TMEM17

Gene ID

5019

200728

Gene name3-oxoacid CoA-transferase 1transmembrane protein 17
SynonymsOXCT|SCOT-
Cytomap

5p13.1

2p15

Type of geneprotein-codingprotein-coding
Descriptionsuccinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial3-oxoacid CoA transferaseSCOT-ssomatic-type succinyl-CoA:3-oxoacid CoA-transferasesuccinyl CoA:3-oxoacid CoA transferasesuccinyl-CoA:3-ketoacid-CoA transferasetransmembrane protein 17
Modification date2018051920180523
UniProtAcc

P55809

Q86X19

Ensembl transtripts involved in fusion geneENST00000196371, ENST00000509987, 
ENST00000512084, ENST00000510634, 
ENST00000513081, 
ENST00000335390, 
Fusion gene scores* DoF score4 X 2 X 4=321 X 1 X 1=1
# samples 41
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: OXCT1 [Title/Abstract] AND TMEM17 [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
TCGARVLUSCTCGA-63-5131-01AOXCT1chr5

41870383

-TMEM17chr2

62729929

-
* 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-shiftENST00000196371ENST00000335390OXCT1chr5

41870383

-TMEM17chr2

62729929

-
intron-3CDSENST00000509987ENST00000335390OXCT1chr5

41870383

-TMEM17chr2

62729929

-
intron-3CDSENST00000512084ENST00000335390OXCT1chr5

41870383

-TMEM17chr2

62729929

-
intron-3CDSENST00000510634ENST00000335390OXCT1chr5

41870383

-TMEM17chr2

62729929

-
intron-3CDSENST00000513081ENST00000335390OXCT1chr5

41870383

-TMEM17chr2

62729929

-

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FusionProtFeatures for OXCT1_TMEM17


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
OXCT1

P55809

TMEM17

Q86X19

Key enzyme for ketone body catabolism. Transfers the CoAmoiety from succinate to acetoacetate. Formation of the enzyme-CoAintermediate proceeds via an unstable anhydride species formedbetween the carboxylate groups of the enzyme and substrate. Transmembrane component of the tectonic-like complex, acomplex localized at the transition zone of primary cilia andacting as a barrier that prevents diffusion of transmembraneproteins between the cilia and plasma membranes. Required forciliogenesis and sonic hedgehog/SHH signaling (By similarity).{ECO:0000250}.

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 OXCT1_TMEM17


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 OXCT1_TMEM17


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
OXCT1PSEN1, TMEM9, SVIL, UBXN7, VMA21, TCOF1, TOR1AIP1, SUCLA2, PLAUR, SDHAF2, SUCLG1, SCAF4, SDHA, SEPT11, PSME1, UQCRFS1, UQCRFS1P1, ATIC, TMEM189, VAPB, TIMM9, TMEM177, CTTN, SGSH, NCL, S100A16, PGK1, IQCB1, ADSS, C12orf10, HSPD1, IDH1, MTPN, NME1, CBX3, MAPK14, PTMS, PTPN11, RBBP7, C11orf58, THOP1, WDR1, AHNAK, FH, HINT1, HSPB1, LYPLA1, MDH1, PRDX6, RAE1, SOD1, TALDO1, TPI1, NTRK1, NDUFV1, OXCT1, OXCT2, PRSS35, PTPMT1, C7orf55, PAK7, NDUFS3, C1QBP, EPS15TMEM17ABCC1, ABCC5, ACBD3, ACSL3, ADD3, ADIPOR1, AGPAT6, AGPAT9, AHCYL1, ALDH3A2, ALG9, ANK3, ANKLE2, ANO6, AP1B1, AP2S1, AP3M1, AP4B1, AP4E1, APPL1, ARCN1, ARFGAP2, ARFGAP3, ARFIP1, ARFIP2, ARHGAP1, ARL13B, ATP11C, ATP1A1, ATP2B1, ATP2C1, ATP6AP1, ATP6AP2, ATP6V1F, ATP7A, AUP1, B9D1, BAIAP2L1, BCAP31, BET1, BET1L, BLZF1, BTF3, VPS51, EMC7, C19orf26, ERICH5, THEM6, RABL6, CACHD1, CAMLG, CASK, CAV1, CCDC115, CCDC47, CD99, CDCA3, CDKAL1, CKAP4, CLCC1, CLCN7, CLINT1, CLNS1A, CNNM2, CNNM3, COG3, COPA, COPE, COPG1, EMC8, CPD, CPNE8, CTNND1, CXADR, CYFIP1, CYP51A1, DDRGK1, DEPDC1B, DHRS7, DLG1, DSC2, DSG2, DVL1, EBAG9, EFNB1, EFNB2, EHBP1, EMD, EPB41L1, EPHA2, EPHB4, EPN1, EPN2, EPS15, ESYT1, ESYT2, EXOC3, FAM129B, FAM171A2, FAM171B, TVP23B, FAM219A, FAM91A1, FERMT2, FLOT2, FLVCR1, FNBP1, FNDC3A, FRS2, FZD5, FZD6, GBAS, GGA1, GGA3, GOLGA5, GOPC, GORAB, GORASP2, GOSR1, GOSR2, GPR107, GPR108, GPR180, GPR89A, HGS, HIP1, HLA-A, HM13, HMOX2, HSPA12A, IGF2R, INSR, IRS4, ITFG3, ITGA6, ITGB1, ITM2B, ITM2C, JAG2, JPH1, JUP, EMC1, KIAA0319L, PALD1, KIAA1715, KIRREL, LBR, LEMD3, LIN7C, LLGL1, LMAN1, LNPEP, LRBA, LRP6, LRP8, LSR, LYN, LYSMD3, MARCKSL1, MARK2, MARK3, MARVELD2, MB21D2, MCAM, MFAP3, MKS1, MMGT1, MOSPD2, MPP1, MPP7, MPZL1, MTMR6, NBEA, NDRG1, NDUFS8, NETO2, NOTCH1, NOTCH2, NSDHL, NUMB, NUP155, OCLN, OCRL, OSBP, OSBPL11, OSBPL8, PACSIN2, PAK4, PALM, PANX1, PCDH7, PDXDC1, PDZD11, PDZD8, PGRMC2, PHACTR4, PKP4, PLD3, PLEKHA1, PLEKHA5, PPFIBP1, PREB, PRKCI, PTK7, PTPN1, PTPN2, PVRL2, RAB11FIP5, RAB23, RAB7A, RABL3, RELL1, RER1, RHBDD2, RHBDD3, ROR1, ROR2, RPF2, SCAMP1, SCAMP2, SCAMP3, SCAMP4, SCARB1, SCFD1, SCRIB, SCYL1, SCYL2, SCYL3, SEC11A, SEC22B, SEC23A, SEC23B, SEC23IP, SEC24A, SEC24B, SEC31A, SEC63, SEMA4C, SEMA6A, SENP2, SHISA2, SLC12A2, SLC12A4, SLC12A6, SLC12A7, SLC19A1, SLC1A3, SLC1A4, SLC1A5, SLC20A1, SLC20A2, SLC29A1, SLC30A1, SLC30A5, SLC30A6, SLC33A1, SLC35B3, SLC35F2, SLC38A1, SLC38A2, SLC39A10, SLC39A14, SLC39A6, SLC3A2, SLC4A7, SLC5A3, SLC5A6, SLC6A15, SLC6A6, SLC6A8, SLC6A9, SLC7A1, SLC7A11, SLC7A2, SLC7A5, SLC9A1, SLCO4A1, SMAP2, SMCR8, SMPD4, SNAP23, SNAP47, SNX2, SNX3, SOAT1, SPCS3, SPRY4, SQSTM1, SRPR, STAM, STAM2, STEAP3, STIM1, STOM, STX10, STX12, STX16, STX5, STX6, STX7, STX8, TBC1D22B, TBC1D5, TFG, TFRC, EMC3, TMEM115, TMEM138, TMEM199, TMEM209, TMEM237, TMEM30A, NDC1, TMEM51, TMEM87A, TMEM9, TMX1, TNFRSF10B, TNIK, TOLLIP, TOR1AIP1, TRIM13, EMC2, UBE2J1, UBIAD1, UBXN4, UNC5B, USO1, USP6NL, VAMP2, VAMP3, VAMP4, VAMP7, VAMP8, VANGL1, VANGL2, VEZT, VKORC1L1, VMA21, VPS45, VRK2, WASF2, WDR11, WDR20, WDR41, WDR6, WDR77, YIF1A, YKT6, YWHAH, ZC3HAV1, ZDHHC20, ZDHHC5, ABCE1, ADCY9, AKAP5, AKT2, APBB1, ATP2B4, CYB5R3, DDX54, DST, EFR3B, EPB41L5, ERBB2IP, EXOC4, FAM171A1, FTSJ1, GCC1, GPRC5A, ISCA1, KIAA1549, KIDINS220, KTN1, LRP2, MAP4K4, NCKAP1, NDUFS3, NSA2, TENM1, PARD3, PIGU, PIK3R1, PKP2, PODXL, PRRT3, PTPN13, RAB11B, RAB2A, RAB5B, RAI14, RASAL2, SLCO4C1, STIM2, TMEM2, TRIP11, UNC5C, UTRN, YES1, LPHN2


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 OXCT1_TMEM17


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 OXCT1_TMEM17


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneOXCT1C0342792Succinyl-CoA:3-oxoacid CoA transferase deficiency3CTD_human;ORPHANET;UNIPROT
HgeneOXCT1C0029456Osteoporosis1CTD_human
TgeneTMEM17C2745997OROFACIODIGITAL SYNDROME VI1UNIPROT