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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: 4222

FusionGeneSummary for BLVRA_STK17A

check button Fusion gene summary
Fusion gene informationFusion gene name: BLVRA_STK17A
Fusion gene ID: 4222
HgeneTgene
Gene symbol

BLVRA

STK17A

Gene ID

644

9263

Gene namebiliverdin reductase Aserine/threonine kinase 17a
SynonymsBLVR|BVR|BVRADRAK1
Cytomap

7p13

7p13

Type of geneprotein-codingprotein-coding
Descriptionbiliverdin reductase ABVR Abiliverdin-IX alpha-reductasetestis tissue sperm-binding protein Li 61nserine/threonine-protein kinase 17ADAP kinase-related apoptosis-inducing protein kinase 1death-associated protein kinase-related 1serine/threonine kinase 17a (apoptosis-inducing)
Modification date2018052320180523
UniProtAcc

P53004

Q9UEE5

Ensembl transtripts involved in fusion geneENST00000265523, ENST00000402924, 
ENST00000462448, ENST00000319357, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 5 X 2=30
# samples 16
** MAII scorelog2(1/1*10)=3.32192809488736log2(6/30*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: BLVRA [Title/Abstract] AND STK17A [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
HgeneBLVRA

GO:0055114

oxidation-reduction process

10858451

TgeneSTK17A

GO:0006468

protein phosphorylation

9786912

TgeneSTK17A

GO:0035556

intracellular signal transduction

9786912


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-C8-A26X-01ABLVRAchr7

43843446

+STK17Achr7

43635500

+
* 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-3UTRENST00000265523ENST00000462448BLVRAchr7

43843446

+STK17Achr7

43635500

+
5CDS-3UTRENST00000265523ENST00000319357BLVRAchr7

43843446

+STK17Achr7

43635500

+
5CDS-3UTRENST00000402924ENST00000462448BLVRAchr7

43843446

+STK17Achr7

43635500

+
5CDS-3UTRENST00000402924ENST00000319357BLVRAchr7

43843446

+STK17Achr7

43635500

+

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FusionProtFeatures for BLVRA_STK17A


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

P53004

STK17A

Q9UEE5

Reduces the gamma-methene bridge of the opentetrapyrrole, biliverdin IX alpha, to bilirubin with theconcomitant oxidation of a NADH or NADPH cofactor. Acts as a positive regulator of apoptosis. Also acts asa regulator of cellular reactive oxygen species.{ECO:0000269|PubMed:21489989, ECO:0000269|PubMed:9786912}.

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 BLVRA_STK17A


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 BLVRA_STK17A


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
BLVRALNX1, TLN1, TBX20, OSBPL6, PCYOX1, ARF5, RTN4IP1, OCIAD1, RRAGB, SNX5, DDHD2, THBS3, NTRK1, DUSP1, DUSP19, P2RY12, DNASE1L2, WDR53, TRIM25STK17ASTK17A, TRIM25


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 BLVRA_STK17A


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 BLVRA_STK17A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBLVRAC0008370Cholestasis1CTD_human;HPO
HgeneBLVRAC0023893Liver Cirrhosis, Experimental1CTD_human