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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: 19558

FusionGeneSummary for LDHB_PEX1

check button Fusion gene summary
Fusion gene informationFusion gene name: LDHB_PEX1
Fusion gene ID: 19558
HgeneTgene
Gene symbol

LDHB

PEX1

Gene ID

3945

339324

Gene namelactate dehydrogenase Bzinc finger protein 260
SynonymsHEL-S-281|LDH-B|LDH-H|LDHBD|TRG-5OZRF1|PEX1|ZFP260
Cytomap

12p12.1

19q13.12

Type of geneprotein-codingprotein-coding
DescriptionL-lactate dehydrogenase B chainLDH heart subunitepididymis secretory protein Li 281lactate dehydrogenase H chainrenal carcinoma antigen NY-REN-46testicular secretory protein Li 25zinc finger protein 260zfp-260
Modification date2018052220180519
UniProtAcc

P07195

O43933

Ensembl transtripts involved in fusion geneENST00000535112, ENST00000396076, 
ENST00000350669, 
ENST00000438045, 
ENST00000248633, ENST00000428214, 
ENST00000541751, 
Fusion gene scores* DoF score6 X 4 X 5=1209 X 6 X 7=378
# samples 69
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/378*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LDHB [Title/Abstract] AND PEX1 [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
TCGARVKIRPTCGA-IA-A40Y-01ALDHBchr12

21788276

-PEX1chr7

92146729

-
* 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
intron-intronENST00000535112ENST00000438045LDHBchr12

21788276

-PEX1chr7

92146729

-
intron-intronENST00000535112ENST00000248633LDHBchr12

21788276

-PEX1chr7

92146729

-
intron-intronENST00000535112ENST00000428214LDHBchr12

21788276

-PEX1chr7

92146729

-
intron-intronENST00000535112ENST00000541751LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000396076ENST00000438045LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000396076ENST00000248633LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000396076ENST00000428214LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000396076ENST00000541751LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000350669ENST00000438045LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000350669ENST00000248633LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000350669ENST00000428214LDHBchr12

21788276

-PEX1chr7

92146729

-
5CDS-intronENST00000350669ENST00000541751LDHBchr12

21788276

-PEX1chr7

92146729

-

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FusionProtFeatures for LDHB_PEX1


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

P07195

PEX1

O43933


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 LDHB_PEX1


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 LDHB_PEX1


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
LDHBLDHB, H2AFX, TERF1, POT1, CUL3, CUL4B, CDK2, COPS5, LDHA, ECT2, LIG4, PAXIP1, SMURF1, CTNNB1, FN1, VCAM1, ATF2, METTL21B, UBL4A, ITGA4, RAD52, CKS2, CKS1B, ALDH7A1, BZW1, CKB, CNDP2, G6PD, GNAI3, HMGB2, HNRNPA2B1, HNRNPAB, FTO, GINS4, PAFAH1B2, PAFAH1B3, SLC9A3R1, TGM2, UBE2V1, NPEPPS, PAK2, PFAS, PGD, RPS6KA1, TXNDC5, UBFD1, YWHAB, YWHAG, YWHAQ, YWHAZ, STAU1, HUWE1, FUS, PEX5, SUZ12, RNF2, ACADM, ADSL, AHCY, ALDH1B1, ALDH2, ALDH4A1, APRT, ARF4, ARF5, ASS1, CAT, CCT3, CCT6A, CCT6B, CTSD, EIF4H, ENO1, ETFA, FAHD1, FH, G3BP1, GAA, GFPT1, IDE, KIAA0368, AHSA1, ARF1, CFL1, CFL2, DNAJA1, DSTN, HSPA9, NANP, PCMT1, PHGDH, RAB1A, RAB1B, RAB5C, SOD1, TKT, UFC1, WDR1, MDH1, MIF, NIT2, NME1-NME2, NME2, NUP50, PARK7, PDHA1, PEPD, PGK1, PGM1, PHB2, PKM, PPIA, PPT1, PRCP, PRDX5, PSMC2, RAB5A, RHEB, SORD, TALDO1, TPI1, UBE2N, NTRK1, PTEN, EWSR1, PPME1, CKAP5, PPP4R1, MCM2, C3orf17, FAM210A, ZNF746, LDHC, COQ2, DLD, DLST, DNM1L, SDHA, SOAT1, TRIM25, BRCA1PEX1PEX26, PEX6, PPP2R1A, RELA, DTWD2, FAS, THBS3, FBXW11, HERC2, SMC1A, EXOSC2, DKKL1, FAM174A, ICAM1


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 LDHB_PEX1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneLDHBP07195DB09118StiripentolL-lactate dehydrogenase B chainsmall moleculeapproved
HgeneLDHBP07195DB11638ArtenimolL-lactate dehydrogenase B chainsmall moleculeapproved|investigational

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RelatedDiseases for LDHB_PEX1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLDHBC3279904Lactate Dehydrogenase B Deficiency7ORPHANET;UNIPROT
HgeneLDHBC0007124Noninfiltrating Intraductal Carcinoma1CTD_human
HgeneLDHBC0007134Renal Cell Carcinoma1CTD_human
HgeneLDHBC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneLDHBC0025521Inborn Errors of Metabolism1CTD_human
HgeneLDHBC0027626Neoplasm Invasiveness1CTD_human
HgeneLDHBC0033578Prostatic Neoplasms1CTD_human
HgeneLDHBC0948089Acute Coronary Syndrome1CTD_human
HgeneLDHBC1458155Mammary Neoplasms1CTD_human
TgenePEX1C0043459Zellweger Syndrome7CTD_human;ORPHANET;UNIPROT
TgenePEX1C0282527Infantile Refsum Disease (disorder)7ORPHANET;UNIPROT
TgenePEX1C1832200Peroxisome biogenesis disorders3CTD_human
TgenePEX1C1856186Deafness enamel hypoplasia nail defects1ORPHANET;UNIPROT