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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: 24884

FusionGeneSummary for NRXN2_GIT1

check button Fusion gene summary
Fusion gene informationFusion gene name: NRXN2_GIT1
Fusion gene ID: 24884
HgeneTgene
Gene symbol

NRXN2

GIT1

Gene ID

9379

28964

Gene nameneurexin 2GIT ArfGAP 1
Synonyms--
Cytomap

11q13.1

17q11.2

Type of geneprotein-codingprotein-coding
Descriptionneurexin-2-betaneurexin IIARF GTPase-activating protein GIT1ARF GAP GIT1CAT-1CAT1G protein-coupled receptor kinase interacting ArfGAP 1G protein-coupled receptor kinase-interactor 1GRK-interacting protein 1cool-associated and tyrosine-phosphorylated protein 1
Modification date2018051920180522
UniProtAcc

Q9P2S2

Q9Y2X7

Ensembl transtripts involved in fusion geneENST00000377559, ENST00000265459, 
ENST00000301894, ENST00000377551, 
ENST00000409571, ENST00000496291, 
ENST00000225394, ENST00000394869, 
ENST00000581348, ENST00000579937, 
Fusion gene scores* DoF score3 X 3 X 2=184 X 4 X 2=32
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: NRXN2 [Title/Abstract] AND GIT1 [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
TgeneGIT1

GO:0032465

regulation of cytokinesis

23108400


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
ChiTaRS3.1BF932395NRXN2chr11

64422578

+GIT1chr17

27901397

-
* 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-3UTRENST00000377559ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000377559ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000377559ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000377559ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000265459ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000265459ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000265459ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000265459ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000301894ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000301894ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000301894ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000301894ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000377551ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000377551ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000377551ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000377551ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000409571ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000409571ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000409571ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000409571ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000496291ENST00000225394NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000496291ENST00000394869NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-3UTRENST00000496291ENST00000581348NRXN2chr11

64422578

+GIT1chr17

27901397

-
intron-intronENST00000496291ENST00000579937NRXN2chr11

64422578

+GIT1chr17

27901397

-

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FusionProtFeatures for NRXN2_GIT1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NRXN2

Q9P2S2

GIT1

Q9Y2X7

Neuronal cell surface protein that may be involved incell recognition and cell adhesion. May mediate intracellularsignaling. GTPase-activating protein for the ADP ribosylationfactor family. May serve as a scaffold to bring together moleculesto form signaling modules controlling vesicle trafficking,adhesion and cytoskeletal organization. Increases the speed ofcell migration, as well as the size and rate of formation ofprotrusions, possibly by targeting PAK1 to adhesions and theleading edge of lamellipodia. Sequesters inactive non-tyrosine-phosphorylated paxillin in cytoplasmic complexes. Involved in theregulation of cytokinesis; the function may involve SDCCAG3 andPTPN13 (By similarity). {ECO:0000250|UniProtKB:Q68FF6,ECO:0000269|PubMed:11896197}.

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 NRXN2_GIT1


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 NRXN2_GIT1


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 NRXN2_GIT1


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 NRXN2_GIT1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNRXN2C0036341Schizophrenia1PSYGENET
HgeneNRXN2C1510586Autism Spectrum Disorders1CTD_human
TgeneGIT1C0025261Memory Disorders1CTD_human
TgeneGIT1C0424295Hyperactive behavior1CTD_human
TgeneGIT1C1263846Attention deficit hyperactivity disorder1CTD_human