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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: 19343

FusionGeneSummary for LAMA2_GRIK2

check button Fusion gene summary
Fusion gene informationFusion gene name: LAMA2_GRIK2
Fusion gene ID: 19343
HgeneTgene
Gene symbol

LAMA2

GRIK2

Gene ID

3908

2901

Gene namelaminin subunit alpha 2glutamate ionotropic receptor kainate type subunit 5
SynonymsLAMMEAA2|GRIK2|GluK5|KA2
Cytomap

6q22.33

19q13.2

Type of geneprotein-codingprotein-coding
Descriptionlaminin subunit alpha-2laminin M chainlaminin, alpha 2laminin-12 subunit alphalaminin-2 subunit alphalaminin-4 subunit alphamerosin heavy chainmutant laminin subunit alpha 2glutamate receptor ionotropic, kainate 5excitatory amino acid receptor 2glutamate receptor KA2
Modification date2018052220180523
UniProtAcc

P24043

Q13002

Ensembl transtripts involved in fusion geneENST00000421865, ENST00000498257, 
ENST00000413795, ENST00000369138, 
ENST00000421544, ENST00000358361, 
ENST00000318991, ENST00000369137, 
ENST00000369134, 
Fusion gene scores* DoF score6 X 5 X 3=905 X 5 X 3=75
# samples 54
** MAII scorelog2(5/90*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/75*10)=-0.906890595608519
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LAMA2 [Title/Abstract] AND GRIK2 [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

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
TCGARVSARCTCGA-HB-A3YV-01ALAMA2chr6

129513998

+GRIK2chr6

102124498

+
* 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-shiftENST00000421865ENST00000413795LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000369138LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000421544LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000358361LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000318991LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000369137LAMA2chr6

129513998

+GRIK2chr6

102124498

+
Frame-shiftENST00000421865ENST00000369134LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000413795LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000369138LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000421544LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000358361LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000318991LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000369137LAMA2chr6

129513998

+GRIK2chr6

102124498

+
intron-3CDSENST00000498257ENST00000369134LAMA2chr6

129513998

+GRIK2chr6

102124498

+

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FusionProtFeatures for LAMA2_GRIK2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LAMA2

P24043

GRIK2

Q13002

Binding to cells via a high affinity receptor, lamininis thought to mediate the attachment, migration and organizationof cells into tissues during embryonic development by interactingwith other extracellular matrix components.

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 LAMA2_GRIK2


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 LAMA2_GRIK2


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
LAMA2DAG1, SMC6, ENTHD2GRIK2SDCBP, PICK1, DLG4, GRIP1, GRID2, DLG1, DLG3, GRIK5, GRIA1, GRIA2, CALCOCO1, TRIM25, PARK2


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 LAMA2_GRIK2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGRIK2Q13002DB00849MethylphenobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved
TgeneGRIK2Q13002DB01354HeptabarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved
TgeneGRIK2Q13002DB01355HexobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved
TgeneGRIK2Q13002DB00306TalbutalGlutamate receptor ionotropic, kainate 2small moleculeapproved|illicit
TgeneGRIK2Q13002DB01351AmobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved|illicit
TgeneGRIK2Q13002DB01352AprobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved|illicit
TgeneGRIK2Q13002DB01353ButethalGlutamate receptor ionotropic, kainate 2small moleculeapproved|illicit
TgeneGRIK2Q13002DB01174PhenobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved|investigational
TgeneGRIK2Q13002DB00312PentobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved|investigational|vet_approved
TgeneGRIK2Q13002DB00142Glutamic AcidGlutamate receptor ionotropic, kainate 2small moleculeapproved|nutraceutical
TgeneGRIK2Q13002DB00418SecobarbitalGlutamate receptor ionotropic, kainate 2small moleculeapproved|vet_approved
TgeneGRIK2Q13002DB00599ThiopentalGlutamate receptor ionotropic, kainate 2small moleculeapproved|vet_approved
TgeneGRIK2Q13002DB00794PrimidoneGlutamate receptor ionotropic, kainate 2small moleculeapproved|vet_approved

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RelatedDiseases for LAMA2_GRIK2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLAMA2C1263858Muscular dystrophy congenital, merosin negative3CTD_human;ORPHANET;UNIPROT
HgeneLAMA2C0026850Muscular Dystrophy2CTD_human;HPO
HgeneLAMA2C0036341Schizophrenia2CTD_human
HgeneLAMA2C0005695Bladder Neoplasm1CTD_human
HgeneLAMA2C0027092Myopia1CTD_human
TgeneGRIK2C0005586Bipolar Disorder3CTD_human;PSYGENET
TgeneGRIK2C0004352Autistic Disorder2CTD_human
TgeneGRIK2C0033953Psychosexual Disorders1CTD_human
TgeneGRIK2C0036341Schizophrenia1CTD_human
TgeneGRIK2C0236969Substance-Related Disorders1CTD_human
TgeneGRIK2C0525045Mood Disorders1PSYGENET