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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: 17665

FusionGeneSummary for IQCG_BPTF

check button Fusion gene summary
Fusion gene informationFusion gene name: IQCG_BPTF
Fusion gene ID: 17665
HgeneTgene
Gene symbol

IQCG

BPTF

Gene ID

84223

2186

Gene nameIQ motif containing Gbromodomain PHD finger transcription factor
SynonymsCFAP122|DRC9FAC1|FALZ|NEDDFL|NURF301
Cytomap

3q29

17q24.2

Type of geneprotein-codingprotein-coding
Descriptiondynein regulatory complex protein 9IQ domain-containing protein Gdynein regulatory complex subunit 9nucleosome-remodeling factor subunit BPTFbromodomain and PHD domain transcription factorbromodomain and PHD finger-containing transcription factorfetal Alz-50 clone 1 proteinfetal Alz-50 reactive clone 1fetal Alzheimer antigennucleosome remodeling f
Modification date2018051920180519
UniProtAcc

Q9H095

Q12830

Ensembl transtripts involved in fusion geneENST00000265239, ENST00000455191, 
ENST00000453254, ENST00000480302, 
ENST00000335221, ENST00000321892, 
ENST00000306378, ENST00000424123, 
ENST00000577770, 
Fusion gene scores* DoF score4 X 4 X 1=1612 X 12 X 4=576
# samples 412
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(12/576*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IQCG [Title/Abstract] AND BPTF [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
TgeneBPTF

GO:0000122

negative regulation of transcription by RNA polymerase II

10727212

TgeneBPTF

GO:0006338

chromatin remodeling

14609955


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
ChiTaRS3.1DA779835IQCGchr3

197681003

+BPTFchr17

65914828

+
* 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-3CDSENST00000265239ENST00000335221IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000265239ENST00000321892IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000265239ENST00000306378IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000265239ENST00000424123IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-intronENST00000265239ENST00000577770IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000455191ENST00000335221IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000455191ENST00000321892IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000455191ENST00000306378IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000455191ENST00000424123IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-intronENST00000455191ENST00000577770IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000453254ENST00000335221IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000453254ENST00000321892IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000453254ENST00000306378IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000453254ENST00000424123IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-intronENST00000453254ENST00000577770IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000480302ENST00000335221IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000480302ENST00000321892IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000480302ENST00000306378IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-3CDSENST00000480302ENST00000424123IQCGchr3

197681003

+BPTFchr17

65914828

+
intron-intronENST00000480302ENST00000577770IQCGchr3

197681003

+BPTFchr17

65914828

+

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FusionProtFeatures for IQCG_BPTF


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

Q9H095

BPTF

Q12830

Component of the nexin-dynein regulatory complex (N-DRC), a key regulator of ciliary/flagellar motility whichmaintains the alignment and integrity of the distal axoneme andregulates microtubule sliding in motile axonemes. Binds calmodulinwhen cellular Ca(2+) levels are low and thereby contributes to theregulation of calcium and calmodulin-dependent protein kinase IV(CAMK4) activity; contributes to the regulation of CAMK4 signalingcascades. Required for normal axoneme assembly in sperm flagella,normal sperm tail formation and for male fertility.{ECO:0000250|UniProtKB:A3KQH2, ECO:0000250|UniProtKB:A8HQ54,ECO:0000250|UniProtKB:Q80W32}. Histone-binding component of NURF (nucleosome-remodelingfactor), a complex which catalyzes ATP-dependent nucleosomesliding and facilitates transcription of chromatin. Specificallyrecognizes H3 tails trimethylated on 'Lys-4' (H3K4me3), which marktranscription start sites of virtually all active genes. May alsoregulate transcription through direct binding to DNA ortranscription factors.

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 IQCG_BPTF


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 IQCG_BPTF


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 IQCG_BPTF


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 IQCG_BPTF


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneBPTFC0005695Bladder Neoplasm1CTD_human