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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: 14010

FusionGeneSummary for FSTL1_ABCB6

check button Fusion gene summary
Fusion gene informationFusion gene name: FSTL1_ABCB6
Fusion gene ID: 14010
HgeneTgene
Gene symbol

FSTL1

ABCB6

Gene ID

11167

10058

Gene namefollistatin like 1ATP binding cassette subfamily B member 6 (Langereis blood group)
SynonymsFRP|FSL1|MIR198|OCC-1|OCC1|tsc36ABC|LAN|MTABC3|PRP|umat
Cytomap

3q13.33

2q35

Type of geneprotein-codingprotein-coding
Descriptionfollistatin-related protein 1follistatin-like protein 1ATP-binding cassette sub-family B member 6, mitochondrialATP-binding cassette half-transporterATP-binding cassette sub-family B member 6ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)P-glycoprotein-related proteinmitoch
Modification date2018051920180523
UniProtAcc

Q12841

Q9NP58

Ensembl transtripts involved in fusion geneENST00000295633, ENST00000424703, 
ENST00000485968, 
ENST00000265316, 
ENST00000439002, 
Fusion gene scores* DoF score8 X 7 X 2=1122 X 2 X 1=4
# samples 82
** MAII scorelog2(8/112*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: FSTL1 [Title/Abstract] AND ABCB6 [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
TgeneABCB6

GO:0006779

porphyrin-containing compound biosynthetic process

17006453

TgeneABCB6

GO:0015886

heme transport

17661442


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
ChiTaRS3.1R74223FSTL1chr3

120113335

-ABCB6chr2

220085176

-
* 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-intronENST00000295633ENST00000265316FSTL1chr3

120113335

-ABCB6chr2

220085176

-
intron-intronENST00000295633ENST00000439002FSTL1chr3

120113335

-ABCB6chr2

220085176

-
intron-intronENST00000424703ENST00000265316FSTL1chr3

120113335

-ABCB6chr2

220085176

-
intron-intronENST00000424703ENST00000439002FSTL1chr3

120113335

-ABCB6chr2

220085176

-
intron-intronENST00000485968ENST00000265316FSTL1chr3

120113335

-ABCB6chr2

220085176

-
intron-intronENST00000485968ENST00000439002FSTL1chr3

120113335

-ABCB6chr2

220085176

-

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FusionProtFeatures for FSTL1_ABCB6


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FSTL1

Q12841

ABCB6

Q9NP58

May modulate the action of some growth factors on cellproliferation and differentiation. Binds heparin (By similarity).{ECO:0000250}. Binds heme and porphyrins and functions in their ATP-dependent uptake into the mitochondria. Plays a crucial role inheme synthesis. {ECO:0000269|PubMed:10837493,ECO:0000269|PubMed:17006453}.

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 FSTL1_ABCB6


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 FSTL1_ABCB6


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 FSTL1_ABCB6


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 FSTL1_ABCB6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFSTL1C0003504Aortic Valve Insufficiency1CTD_human
HgeneFSTL1C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneFSTL1C0036341Schizophrenia1PSYGENET
HgeneFSTL1C0043094Weight Gain1CTD_human
HgeneFSTL1C2609414Acute kidney injury1CTD_human
TgeneABCB6C3809394DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 34UNIPROT
TgeneABCB6C1836705Pseudohyperkalemia, Familial, 2, due to Red Cell Leak2ORPHANET;UNIPROT
TgeneABCB6C0009404Colorectal Neoplasms1CTD_human
TgeneABCB6C0032460Polycystic Ovary Syndrome1CTD_human
TgeneABCB6C3281027MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 71UNIPROT