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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: 4411

FusionGeneSummary for BRD4_SLC1A6

check button Fusion gene summary
Fusion gene informationFusion gene name: BRD4_SLC1A6
Fusion gene ID: 4411
HgeneTgene
Gene symbol

BRD4

SLC1A6

Gene ID

23476

6511

Gene namebromodomain containing 4solute carrier family 1 member 6
SynonymsCAP|HUNK1|HUNKI|MCAPEAAT4
Cytomap

19p13.12

19p13.12

Type of geneprotein-codingprotein-coding
Descriptionbromodomain-containing protein 4chromosome-associated proteinexcitatory amino acid transporter 4sodium-dependent glutamate/aspartate transportersolute carrier family 1 (high affinity aspartate/glutamate transporter), member 6
Modification date2018052220180519
UniProtAcc

O60885

P48664

Ensembl transtripts involved in fusion geneENST00000263377, ENST00000371835, 
ENST00000360016, ENST00000602230, 
ENST00000430939, ENST00000221742, 
ENST00000600144, ENST00000598504, 
ENST00000544886, 
Fusion gene scores* DoF score14 X 6 X 10=8407 X 3 X 7=147
# samples 198
** MAII scorelog2(19/840*10)=-2.14438990933517
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/147*10)=-0.877744249949002
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BRD4 [Title/Abstract] AND SLC1A6 [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
HgeneBRD4

GO:0032968

positive regulation of transcription elongation from RNA polymerase II promoter

19103749|23086925

HgeneBRD4

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

19103749

HgeneBRD4

GO:0045944

positive regulation of transcription by RNA polymerase II

23086925|23317504

HgeneBRD4

GO:0050727

regulation of inflammatory response

19103749

HgeneBRD4

GO:1901407

regulation of phosphorylation of RNA polymerase II C-terminal domain

23086925


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
TCGALDCESCTCGA-C5-A7X5-01ABRD4chr19

15443101

-SLC1A6chr19

15083729

-
* 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-3CDSENST00000263377ENST00000430939BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-3CDSENST00000263377ENST00000221742BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000263377ENST00000600144BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000263377ENST00000598504BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000263377ENST00000544886BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-3CDSENST00000371835ENST00000430939BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-3CDSENST00000371835ENST00000221742BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000371835ENST00000600144BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000371835ENST00000598504BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000371835ENST00000544886BRD4chr19

15443101

-SLC1A6chr19

15083729

-
5UTR-3CDSENST00000360016ENST00000430939BRD4chr19

15443101

-SLC1A6chr19

15083729

-
5UTR-3CDSENST00000360016ENST00000221742BRD4chr19

15443101

-SLC1A6chr19

15083729

-
5UTR-5UTRENST00000360016ENST00000600144BRD4chr19

15443101

-SLC1A6chr19

15083729

-
5UTR-5UTRENST00000360016ENST00000598504BRD4chr19

15443101

-SLC1A6chr19

15083729

-
5UTR-5UTRENST00000360016ENST00000544886BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-3CDSENST00000602230ENST00000430939BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-3CDSENST00000602230ENST00000221742BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000602230ENST00000600144BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000602230ENST00000598504BRD4chr19

15443101

-SLC1A6chr19

15083729

-
intron-5UTRENST00000602230ENST00000544886BRD4chr19

15443101

-SLC1A6chr19

15083729

-

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FusionProtFeatures for BRD4_SLC1A6


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
BRD4

O60885

SLC1A6

P48664

Chromatin reader protein that recognizes and bindsacetylated histones and plays a key role in transmission ofepigenetic memory across cell divisions and transcriptionregulation. Remains associated with acetylated chromatinthroughout the entire cell cycle and provides epigenetic memoryfor postmitotic G1 gene transcription by preserving acetylatedchromatin status and maintaining high-order chromatin structure.During interphase, plays a key role in regulating thetranscription of signal-inducible genes by associating with the P-TEFb complex and recruiting it to promoters: BRD4 is required toform the transcriptionally active P-TEFb complex by displacingnegative regulators such as HEXIM1 and 7SKsnRNA complex from P-TEFb, thereby transforming it into an active form that can thenphosphorylate the C-terminal domain (CTD) of RNA polymerase II.Promotes phosphorylation of 'Ser-2' of the C-terminal domain (CTD)of RNA polymerase II. According to a report, directly acts as anatypical protein kinase and mediates phosphorylation of 'Ser-2' ofthe C-terminal domain (CTD) of RNA polymerase II; these datahowever need additional evidences in vivo (PubMed:22509028). Inaddition to acetylated histones, also recognizes and bindsacetylated RELA, leading to further recruitment of the P-TEFbcomplex and subsequent activation of NF-kappa-B. Also acts as aregulator of p53/TP53-mediated transcription: followingphosphorylation by CK2, recruited to p53/TP53 specific targetpromoters. {ECO:0000269|PubMed:22509028}. Isoform B: Acts as a chromatin insulator in the DNAdamage response pathway. Inhibits DNA damage response signaling byrecruiting the condensin-2 complex to acetylated histones, leadingto chromatin structure remodeling, insulating the region from DNAdamage response by limiting spreading of histone H2AFX/H2A.xphosphorylation. Sodium-dependent, high-affinity amino acid transporterthat mediates the uptake of L-glutamate and also L-aspartate andD-aspartate (PubMed:7791878). Functions as a symporter thattransports one amino acid molecule together with two or threeNa(+) ions and one proton, in parallel with the counter-transportof one K(+) ion. Mediates Cl(-) flux that is not coupled to aminoacid transport; this avoids the accumulation of negative chargesdue to aspartate and Na(+) symport (By similarity). Plays aredundant role in the rapid removal of released glutamate from thesynaptic cleft, which is essential for terminating thepostsynaptic action of glutamate (Probable).{ECO:0000250|UniProtKB:O35921, ECO:0000269|PubMed:7791878,ECO:0000305}.

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 BRD4_SLC1A6


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 BRD4_SLC1A6


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
BRD4RFC1, RFC2, RFC3, RFC4, RFC5, HIST4H4, SIPA1, MED12, MED14, MED24, MED17, CCNT1, CDK9, CCNT2, HEXIM1, HIST2H3C, HIST2H4A, KDM5B, EP300, AFF1, MESDC2, C8orf33, HIST1H3A, HIST1H4A, KAT8, YWHAZ, YWHAE, MED1, CHD4, JMJD6, BAIAP2, BAIAP2L1, RBM25, BRD3, BRD2, WHSC1, GLTSCR1, ATAD5, SMARCA4, ZNF592, BRD9, WHSC1L1, SIRT1, SIRT5, AK1, PGAM2, LDHC, CKM, ELAVL1, MYC, MLLT1, RPL6, PRPF40A, RN7SK, TCERG1, STAT3, GPSM1, FAM90A1, CYP1A1, AP3M1, NUMA1, DMAP1, RTF1, ZC3H18, MMGT1, SMC1A, CDC5L, CHD8, PTAR1, BRCA1, PTEN, FGFR3, KDM5C, DHFR, RB1, MAP2K1, PIP4K2A, CAMKV, CHEK2, CHEK1, WEE1, CDC7, INO80B, TRIM25, CUL1, CUL3, SPOP, AR, ERGSLC1A6ARIH2


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 BRD4_SLC1A6


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneSLC1A6P48664DB00142Glutamic AcidExcitatory amino acid transporter 4small moleculeapproved|nutraceutical

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RelatedDiseases for BRD4_SLC1A6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBRD4C0017636Glioblastoma2CTD_human
HgeneBRD4C0002170Alopecia1CTD_human
HgeneBRD4C0009375Colonic Neoplasms1CTD_human
HgeneBRD4C0020507Hyperplasia1CTD_human
HgeneBRD4C0020542Pulmonary Hypertension1CTD_human
HgeneBRD4C0025149Medulloblastoma1CTD_human
HgeneBRD4C0029463Osteosarcoma1CTD_human
HgeneBRD4C0033578Prostatic Neoplasms1CTD_human
HgeneBRD4C0040136Thyroid Neoplasm1CTD_human
HgeneBRD4C0085413Polycystic Kidney, Autosomal Dominant1CTD_human
TgeneSLC1A6C0005586Bipolar Disorder1PSYGENET
TgeneSLC1A6C0036341Schizophrenia1PSYGENET
TgeneSLC1A6C0041696Unipolar Depression1PSYGENET
TgeneSLC1A6C1269683Major Depressive Disorder1PSYGENET