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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: 32274

FusionGeneSummary for RSBN1L_DTNBP1

check button Fusion gene summary
Fusion gene informationFusion gene name: RSBN1L_DTNBP1
Fusion gene ID: 32274
HgeneTgene
Gene symbol

RSBN1L

DTNBP1

Gene ID

222194

84062

Gene nameround spermatid basic protein 1 likedystrobrevin binding protein 1
Synonyms-BLOC1S8|DBND|HPS7|My031|SDY
Cytomap

7q11.23

6p22.3

Type of geneprotein-codingprotein-coding
Descriptionround spermatid basic protein 1-like proteindysbindinBLOC-1 subunit 8Hermansky-Pudlak syndrome 7 proteinbiogenesis of lysosomal organelles complex-1, subunit 8biogenesis of lysosome-related organelles complex 1 subunit 8dysbindin-1
Modification date2018051920180522
UniProtAcc

Q6PCB5

Q96EV8

Ensembl transtripts involved in fusion geneENST00000334955, ENST00000445288, 
ENST00000344537, ENST00000355917, 
ENST00000338950, ENST00000462989, 
Fusion gene scores* DoF score5 X 3 X 4=609 X 5 X 7=315
# samples 59
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/315*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RSBN1L [Title/Abstract] AND DTNBP1 [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
TgeneDTNBP1

GO:0031175

neuron projection development

16980328


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
TCGALDBRCATCGA-C8-A12V-01ARSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
* 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
Frame-shiftENST00000334955ENST00000344537RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
Frame-shiftENST00000334955ENST00000355917RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
Frame-shiftENST00000334955ENST00000338950RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
5CDS-intronENST00000334955ENST00000462989RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
intron-3CDSENST00000445288ENST00000344537RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
intron-3CDSENST00000445288ENST00000355917RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
intron-3CDSENST00000445288ENST00000338950RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-
intron-intronENST00000445288ENST00000462989RSBN1Lchr7

77326372

+DTNBP1chr6

15652371

-

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FusionProtFeatures for RSBN1L_DTNBP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RSBN1L

Q6PCB5

DTNBP1

Q96EV8

Component of the BLOC-1 complex, a complex that isrequired for normal biogenesis of lysosome-related organelles(LRO), such as platelet dense granules and melanosomes. In concertwith the AP-3 complex, the BLOC-1 complex is required to targetmembrane protein cargos into vesicles assembled at cell bodies fordelivery into neurites and nerve terminals. The BLOC-1 complex, inassociation with SNARE proteins, is also proposed to be involvedin neurite extension. Associates with the BLOC-2 complex tofacilitate the transport of TYRP1 independent of AP-3 function.Plays a role in synaptic vesicle trafficking and inneurotransmitter release. Plays a role in the regulation of cellsurface exposure of DRD2. May play a role in actin cytoskeletonreorganization and neurite outgrowth. May modulate MAPK8phosphorylation. Appears to promote neuronal transmission andviability through regulating the expression of SNAP25 and SYN1,modulating PI3-kinase-Akt signaling and influencing glutamatergicrelease. Regulates the expression of SYN1 through binding to itspromoter. Modulates prefrontal cortical activity via thedopamine/D2 pathway. {ECO:0000269|PubMed:15345706,ECO:0000269|PubMed:16837549, ECO:0000269|PubMed:17182842,ECO:0000269|PubMed:17989303, ECO:0000269|PubMed:19094965,ECO:0000269|PubMed:20180862, ECO:0000269|PubMed:20921223}.

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 RSBN1L_DTNBP1


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 RSBN1L_DTNBP1


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
RSBN1LTERF1, TERF2, DRG2, ZDHHC17, RPL14, RPL8, EAF1, ZBTB38, ZRANB2, NTRK1, AKAP5, SAMHD1, NEIL3, PAPD5, FBXW7, RSBN1, PNN, CLK2, SRRM2, NKAP, RBM34, RNPS1, CDX1, TRIM25DTNBP1ABI3, ARFIP2, CCND3, DGCR6L, BLOC1S6, BLOC1S5, SNAPIN, BLOC1S1, BLOC1S2, BLOC1S3, OSBPL9, NBEA, IPO5, AKAP6, BRF1, TRIM9, RAB11A, EXOC7, PSME3, ZNF490, DST, GLTSCR1L, KIAA0408, SYNE1, EXOC4, SYBU, SFR1, DCTN1, TRAF3IP1, NUF2, MACF1, KALRN, SRGAP3, RBSN, CCNA2, TRIM2, TRIM32, NDN, DTNB, KIFC3, TRIM27, SDCBP, CCDC53, CCHCR1, C19orf66, BRK1, CCDC146, ELOVL7, IFT20, HAUS1, TXLNB, CCDC153, P4HA3, KANSL1, SSC5D, TEX35, TRIM74, C9orf16, VPS53, AP3M1, NCKAP1, IQGAP2, EXOC3, ASPM, PCNT, COG6, BLOC1S4, AP3D1, VPRBP, TACC1, BRCA2, SNTB2, KTN1, MYO5A, MYO5C, CCDC132, KIF5A, KIF5B, LAMC2, CYFIP2, CYFIP1, KIF3A, DTNA, VPS51, AP3B2, AP3B1, NAV1, STX5, CDK5RAP2, KLC2, KLC1, CETN3, COG5, ALMS1, CEP290, SLC25A16, ARFGEF2, EXOC5, EXOC6, SPAG5, FAM83H, BCAS4, MEF2BNB, CCDC22, AP3S1, C17orf59, COG7, STX8, SDCCAG3, EXOC1, VAMP8, KXD1, VTI1B, TSSC1, ABI1, TRAF7, EXOC6B, NHSL2, AP3S2, SNX7, COPZ1, COPE, XPO1, PTPRM, CCND2, CCND1, TRIM69, TSKS, GGA1, AKNAD1, TRAK2, TRIML2


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 RSBN1L_DTNBP1


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 RSBN1L_DTNBP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDTNBP1C0005586Bipolar Disorder5PSYGENET
TgeneDTNBP1C0041696Unipolar Depression5PSYGENET
TgeneDTNBP1C1269683Major Depressive Disorder5PSYGENET
TgeneDTNBP1C0011570Mental Depression4PSYGENET
TgeneDTNBP1C0011581Depressive disorder4PSYGENET
TgeneDTNBP1C0525045Mood Disorders3PSYGENET
TgeneDTNBP1C0270458Severe major depression with psychotic features2PSYGENET
TgeneDTNBP1C0001973Alcoholic Intoxication, Chronic1PSYGENET
TgeneDTNBP1C0004936Mental disorders1CTD_human
TgeneDTNBP1C0033937Psychoses, Drug1PSYGENET
TgeneDTNBP1C0036341Schizophrenia1CTD_human