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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: 16025

FusionGeneSummary for HEBP1_CREBL2

check button Fusion gene summary
Fusion gene informationFusion gene name: HEBP1_CREBL2
Fusion gene ID: 16025
HgeneTgene
Gene symbol

HEBP1

CREBL2

Gene ID

50865

1389

Gene nameheme binding protein 1cAMP responsive element binding protein like 2
SynonymsHBP|HEBP-
Cytomap

12p13.1

12p13.1

Type of geneprotein-codingprotein-coding
Descriptionheme-binding protein 1p22HBPcAMP-responsive element-binding protein-like 2MHBs-binding protein 1
Modification date2018052320180519
UniProtAcc

Q9NRV9

O60519

Ensembl transtripts involved in fusion geneENST00000014930, ENST00000540916, 
ENST00000536942, 
ENST00000540224, 
ENST00000228865, 
Fusion gene scores* DoF score3 X 2 X 2=125 X 2 X 4=40
# samples 34
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/40*10)=0
Context

PubMed: HEBP1 [Title/Abstract] AND CREBL2 [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
TCGARVLUADTCGA-MP-A4SV-01AHEBP1chr12

13152971

-CREBL2chr12

12788711

+
* 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-3UTRENST00000014930ENST00000540224HEBP1chr12

13152971

-CREBL2chr12

12788711

+
5CDS-3UTRENST00000014930ENST00000228865HEBP1chr12

13152971

-CREBL2chr12

12788711

+
intron-3UTRENST00000540916ENST00000540224HEBP1chr12

13152971

-CREBL2chr12

12788711

+
intron-3UTRENST00000540916ENST00000228865HEBP1chr12

13152971

-CREBL2chr12

12788711

+
5CDS-3UTRENST00000536942ENST00000540224HEBP1chr12

13152971

-CREBL2chr12

12788711

+
5CDS-3UTRENST00000536942ENST00000228865HEBP1chr12

13152971

-CREBL2chr12

12788711

+

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FusionProtFeatures for HEBP1_CREBL2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HEBP1

Q9NRV9

CREBL2

O60519

May bind free porphyrinogens that may be present in thecell and thus facilitate removal of these potentially toxiccompound. Binds with a high affinity to one molecule of heme orporphyrins. It binds metalloporphyrins, free porphyrins and N-methylprotoporphyrin with similar affinities.{ECO:0000269|PubMed:12413491}. Probable regulator of CREB1 transcriptional activitywhich is involved in adipose cells differentiation. May also playa regulatory role in the cell cycle. Identification in achromosomal region frequently deleted in various cancers suggeststhat it might act as a tumor suppressor.{ECO:0000269|PubMed:9693048}.

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 HEBP1_CREBL2


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 HEBP1_CREBL2


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
HEBP1DHX36, COTL1, PCBP1, S100A6, SNX3, UBE2L3, C15orf48, COQ9CREBL2ELAVL1, DNMT3L


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 HEBP1_CREBL2


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 HEBP1_CREBL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource