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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: 6232

FusionGeneSummary for CD68_SH3BGRL

check button Fusion gene summary
Fusion gene informationFusion gene name: CD68_SH3BGRL
Fusion gene ID: 6232
HgeneTgene
Gene symbol

CD68

SH3BGRL

Gene ID

968

6451

Gene nameCD68 moleculeSH3 domain binding glutamate rich protein like
SynonymsGP110|LAMP4|SCARD1HEL-S-115|SH3BGR
Cytomap

17p13.1

Xq21.1

Type of geneprotein-codingprotein-coding
DescriptionmacrosialinCD68 antigenmacrophage antigen CD68scavenger receptor class D, member 1SH3 domain-binding glutamic acid-rich-like proteinSH3 domain binding glutamic acid-rich protein likeSH3-binding domain glutamic acid-rich protein likeepididymis secretory protein Li 115
Modification date2018052020180522
UniProtAcc

P34810

O75368

Ensembl transtripts involved in fusion geneENST00000250092, ENST00000380498, 
ENST00000373212, ENST00000481106, 
Fusion gene scores* DoF score5 X 5 X 1=253 X 2 X 3=18
# samples 53
** MAII scorelog2(5/25*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CD68 [Title/Abstract] AND SH3BGRL [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
ChiTaRS3.1BP305239CD68chr17

7483365

+SH3BGRLchrX

80553880

+
* 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-3UTRENST00000250092ENST00000373212CD68chr17

7483365

+SH3BGRLchrX

80553880

+
5CDS-intronENST00000250092ENST00000481106CD68chr17

7483365

+SH3BGRLchrX

80553880

+
5CDS-3UTRENST00000380498ENST00000373212CD68chr17

7483365

+SH3BGRLchrX

80553880

+
5CDS-intronENST00000380498ENST00000481106CD68chr17

7483365

+SH3BGRLchrX

80553880

+

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FusionProtFeatures for CD68_SH3BGRL


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CD68

P34810

SH3BGRL

O75368

Could play a role in phagocytic activities of tissuemacrophages, both in intracellular lysosomal metabolism andextracellular cell-cell and cell-pathogen interactions. Binds totissue- and organ-specific lectins or selectins, allowing homingof macrophage subsets to particular sites. Rapid recirculation ofCD68 from endosomes and lysosomes to the plasma membrane may allowmacrophages to crawl over selectin-bearing substrates or othercells.

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 CD68_SH3BGRL


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 CD68_SH3BGRL


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


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 CD68_SH3BGRL


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 CD68_SH3BGRL


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCD68C0000786Spontaneous abortion1CTD_human
HgeneCD68C0003872Arthritis, Psoriatic1CTD_human
HgeneCD68C0011853Diabetes Mellitus, Experimental1CTD_human
HgeneCD68C0022116Ischemia1CTD_human
HgeneCD68C0022661Kidney Failure, Chronic1CTD_human
HgeneCD68C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneCD68C1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human