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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: 21887

FusionGeneSummary for MICAL3_SLC1A3

check button Fusion gene summary
Fusion gene informationFusion gene name: MICAL3_SLC1A3
Fusion gene ID: 21887
HgeneTgene
Gene symbol

MICAL3

SLC1A3

Gene ID

57553

6507

Gene namemicrotubule associated monooxygenase, calponin and LIM domain containing 3solute carrier family 1 member 3
SynonymsMICAL-3EA6|EAAT1|GLAST|GLAST1
Cytomap

22q11.21

5p13.2

Type of geneprotein-codingprotein-coding
Description[F-actin]-monooxygenase MICAL3F-actin-monooxygenase MICAL3[F-actin]-methionine sulfoxide oxidase MICAL3flavoprotein oxidoreductase MICAL3molecule interacting with CasL protein 3protein MICAL-3protein-methionine sulfoxide oxidase MICAL3excitatory amino acid transporter 1GLAST-1sodium-dependent glutamate/aspartate transporter 1solute carrier family 1 (glial high affinity glutamate transporter), member 3
Modification date2018051920180519
UniProtAcc

Q7RTP6

P43003

Ensembl transtripts involved in fusion geneENST00000441493, ENST00000400561, 
ENST00000444520, ENST00000414725, 
ENST00000383094, ENST00000207726, 
ENST00000429452, ENST00000585038, 
ENST00000580469, 
ENST00000265113, 
ENST00000506725, ENST00000381918, 
Fusion gene scores* DoF score9 X 6 X 7=37810 X 9 X 6=540
# samples 1012
** MAII scorelog2(10/378*10)=-1.91838623444635
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/540*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MICAL3 [Title/Abstract] AND SLC1A3 [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
HgeneMICAL3

GO:0007010

cytoskeleton organization

24440334

HgeneMICAL3

GO:0030042

actin filament depolymerization

24440334

TgeneSLC1A3

GO:0015813

L-glutamate transmembrane transport

26690923

TgeneSLC1A3

GO:0051938

L-glutamate import

7521911

TgeneSLC1A3

GO:0070779

D-aspartate import across plasma membrane

7521911

TgeneSLC1A3

GO:0071805

potassium ion transmembrane transport

20477940

TgeneSLC1A3

GO:0098712

L-glutamate import across plasma membrane

26690923

TgeneSLC1A3

GO:0140009

L-aspartate import across plasma membrane

20477940

TgeneSLC1A3

GO:1902476

chloride transmembrane transport

20477940


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
ChiTaRS3.1BE936478MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
* 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-intronENST00000441493ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000441493ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000441493ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000400561ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000400561ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000400561ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000444520ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000444520ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000444520ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000414725ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000414725ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000414725ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000383094ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000383094ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000383094ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000207726ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000207726ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000207726ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000429452ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000429452ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000429452ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000585038ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000585038ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000585038ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000580469ENST00000265113MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000580469ENST00000506725MICAL3chr22

18272609

-SLC1A3chr5

36662106

-
intron-intronENST00000580469ENST00000381918MICAL3chr22

18272609

-SLC1A3chr5

36662106

-

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FusionProtFeatures for MICAL3_SLC1A3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MICAL3

Q7RTP6

SLC1A3

P43003

Monooxygenase that promotes depolymerization of F-actinby mediating oxidation of specific methionine residues on actin toform methionine-sulfoxide, resulting in actin filament disassemblyand preventing repolymerization. In the absence of actin, it alsofunctions as a NADPH oxidase producing H(2)O(2). Seems to act asRab effector protein and plays a role in vesicle trafficking.Involved in exocytic vesicles tethering and fusion: themonooxygenase activity is required for this process and implicatesRAB8A associated with exocytotic vesicles. Required forcytokinesis. Contributes to stabilization and/or maturation of theintercellular bridge independently of its monooxygenase activity.Promotes recruitment of Rab8 and ERC1 to the intercellular bridge,and together these proteins are proposed to function in timelyabscission. {ECO:0000269|PubMed:21596566,ECO:0000269|PubMed:24440334}. Sodium-dependent, high-affinity amino acid transporterthat mediates the uptake of L-glutamate and also L-aspartate andD-aspartate (PubMed:7521911, PubMed:8123008, PubMed:20477940,PubMed:26690923, PubMed:28032905, PubMed:28424515). Functions as asymporter that transports one amino acid molecule together withtwo or three Na(+) ions and one proton, in parallel with thecounter-transport of one K(+) ion (PubMed:20477940). MediatesCl(-) flux that is not coupled to amino acid transport; thisavoids the accumulation of negative charges due to aspartate andNa(+) symport (PubMed:20477940). Plays a redundant role in therapid removal of released glutamate from the synaptic cleft, whichis essential for terminating the postsynaptic action of glutamate(By similarity). {ECO:0000250|UniProtKB:P56564,ECO:0000269|PubMed:20477940, ECO:0000269|PubMed:26690923,ECO:0000269|PubMed:28032905, ECO:0000269|PubMed:28424515,ECO:0000269|PubMed:7521911, ECO:0000269|PubMed:8123008}.

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 MICAL3_SLC1A3


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 MICAL3_SLC1A3


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 MICAL3_SLC1A3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneSLC1A3P43003DB00142Glutamic AcidExcitatory amino acid transporter 1 {ECO:0000303|PubMed:16042756, ECO:0000303|PubMed:8647279}small moleculeapproved|nutraceutical

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RelatedDiseases for MICAL3_SLC1A3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSLC1A3C0036341Schizophrenia4PSYGENET
TgeneSLC1A3C0004352Autistic Disorder1CTD_human
TgeneSLC1A3C0005586Bipolar Disorder1PSYGENET
TgeneSLC1A3C0014544Epilepsy1CTD_human;HPO
TgeneSLC1A3C0178417Anhedonia1PSYGENET
TgeneSLC1A3C2675211EPISODIC ATAXIA, TYPE 6 (disorder)1CTD_human;ORPHANET;UNIPROT