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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: 20580

FusionGeneSummary for MAGI1_TBC1D30

check button Fusion gene summary
Fusion gene informationFusion gene name: MAGI1_TBC1D30
Fusion gene ID: 20580
HgeneTgene
Gene symbol

MAGI1

TBC1D30

Gene ID

154043

23329

Gene nameCNKSR family member 3TBC1 domain family member 30
SynonymsCNK3|CNK3/IPCEF1|MAGI1-
Cytomap

6q25.2

12q14.3

Type of geneprotein-codingprotein-coding
Descriptionconnector enhancer of kinase suppressor of ras 3CNK homolog protein 3connector enhancer of KSR 3maguin-like proteinmembrane associated guanylate kinase, WW and PDZ domain containing 1membrane-associated guanylate kinase-interacting protein-like 1TBC1 domain family member 30
Modification date2018052220180523
UniProtAcc

Q96QZ7

Q9Y2I9

Ensembl transtripts involved in fusion geneENST00000330909, ENST00000402939, 
ENST00000483466, ENST00000497477, 
ENST00000470990, 
ENST00000542120, 
ENST00000229088, ENST00000456757, 
ENST00000539867, 
Fusion gene scores* DoF score10 X 6 X 6=36011 X 6 X 7=462
# samples 1010
** MAII scorelog2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/462*10)=-2.20789285164133
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MAGI1 [Title/Abstract] AND TBC1D30 [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
TgeneTBC1D30

GO:0043547

positive regulation of GTPase activity

17646400


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
TCGALDPRADTCGA-KK-A8II-01AMAGI1chr3

66023671

-TBC1D30chr12

65221615

+
* 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-5UTRENST00000330909ENST00000542120MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000330909ENST00000229088MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000330909ENST00000456757MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000330909ENST00000539867MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000402939ENST00000542120MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000402939ENST00000229088MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000402939ENST00000456757MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000402939ENST00000539867MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000483466ENST00000542120MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000483466ENST00000229088MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000483466ENST00000456757MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000483466ENST00000539867MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000497477ENST00000542120MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-5UTRENST00000497477ENST00000229088MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000497477ENST00000456757MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
5CDS-intronENST00000497477ENST00000539867MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
intron-5UTRENST00000470990ENST00000542120MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
intron-5UTRENST00000470990ENST00000229088MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
intron-intronENST00000470990ENST00000456757MAGI1chr3

66023671

-TBC1D30chr12

65221615

+
intron-intronENST00000470990ENST00000539867MAGI1chr3

66023671

-TBC1D30chr12

65221615

+

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FusionProtFeatures for MAGI1_TBC1D30


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MAGI1

Q96QZ7

TBC1D30

Q9Y2I9

May play a role as scaffolding protein at cell-celljunctions. May regulate acid-induced ASIC3 currents by modulatingits expression at the cell surface (By similarity). {ECO:0000250}. GTPase-activating protein (GAP) with broad specificity.Acts as a GAP for RAB3A. Also exhibits significant GAP activitytoward RAB22A, RAB27A, and RAB35 in vitro.

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 MAGI1_TBC1D30


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 MAGI1_TBC1D30


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
MAGI1CTNNB1, LRP2, ASIC3, BZW1, SFN, FCHSD2, WBP1, WBP2, CDH1, NET1, SYNPO, ACTN4, ATN1, BAI1, RAC1, DDN, SSTR3, IGSF5, LATS1, LATS2, RAPGEF2, MOV10, NXF1, CYYR1, LDLRAD4, PTPN14, KCTD3, KIF13B, ZBTB21, KSR1, GIGYF1, LRFN1, DENND1A, SH3PXD2A, SRGAP2, EIF4E2, SIPA1L1, LIMA1, TESK2, DCLK1, ZNF638, RTKN, MAST3, SRSF12, PPM1H, SYDE1, DENND4C, AGAP1, CDC25B, CDK16, FAM110B, USP21, MAPKAP1, FAM53C, ANKRD34A, CGN, FAM110A, HDAC4, NF1, TBC1D25, NADK, CBY1, TIAM1, PHLDB2, KIAA1804, RASAL2, CAMSAP2, LPIN3, GAB2, CDC25C, MELK, PLEKHA7, KIF1C, GIGYF2, DEPDC1B, NAV1, DENND4A, MLLT4, STARD13, RPTOR, SH3RF3, PLEKHA5, SH3BP4, HDAC7, EDC3, LARP1, RAB3IP, INPP5ETBC1D30STX3, MYO5B, SYTL4, EXOC6, SCOC, TRIM25


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 MAGI1_TBC1D30


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 MAGI1_TBC1D30


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMAGI1C0005586Bipolar Disorder2PSYGENET
HgeneMAGI1C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneMAGI1C0036341Schizophrenia1PSYGENET
HgeneMAGI1C1839839MAJOR AFFECTIVE DISORDER 21PSYGENET