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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: 35801

FusionGeneSummary for SPRED2_NAPG

check button Fusion gene summary
Fusion gene informationFusion gene name: SPRED2_NAPG
Fusion gene ID: 35801
HgeneTgene
Gene symbol

SPRED2

NAPG

Gene ID

200734

8774

Gene namesprouty related EVH1 domain containing 2NSF attachment protein gamma
SynonymsSpred-2GAMMASNAP
Cytomap

2p14

18p11.22

Type of geneprotein-codingprotein-coding
Descriptionsprouty-related, EVH1 domain-containing protein 2sprouty protein with EVH-1 domain 2, related sequencegamma-soluble NSF attachment proteinN-ethylmaleimide-sensitive factor attachment protein, gammaSNAP-gammasoluble NSF attachment protein
Modification date2018051920180523
UniProtAcc

Q7Z698

Q99747

Ensembl transtripts involved in fusion geneENST00000356388, ENST00000443619, 
ENST00000474228, 
ENST00000542979, 
ENST00000322897, 
Fusion gene scores* DoF score5 X 3 X 5=752 X 2 X 2=8
# samples 62
** MAII scorelog2(6/75*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: SPRED2 [Title/Abstract] AND NAPG [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
TCGARVLGGTCGA-DB-5277-01ASPRED2chr2

65659096

-NAPGchr18

10530767

+
* 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-intronENST00000356388ENST00000542979SPRED2chr2

65659096

-NAPGchr18

10530767

+
5CDS-intronENST00000356388ENST00000322897SPRED2chr2

65659096

-NAPGchr18

10530767

+
intron-intronENST00000443619ENST00000542979SPRED2chr2

65659096

-NAPGchr18

10530767

+
intron-intronENST00000443619ENST00000322897SPRED2chr2

65659096

-NAPGchr18

10530767

+
intron-intronENST00000474228ENST00000542979SPRED2chr2

65659096

-NAPGchr18

10530767

+
intron-intronENST00000474228ENST00000322897SPRED2chr2

65659096

-NAPGchr18

10530767

+

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FusionProtFeatures for SPRED2_NAPG


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SPRED2

Q7Z698

NAPG

Q99747

Negatively regulates Ras signaling pathways anddownstream activation of MAP kinases.{ECO:0000269|PubMed:15683364}. Required for vesicular transport between the endoplasmicreticulum and the Golgi apparatus.

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 SPRED2_NAPG


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 SPRED2_NAPG


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
SPRED2TESK1, ELAVL1, NBR1, SQSTM1, TOP3B, SPG21, ZDHHC17, PDP1, DPP9, PRTFDC1, RPS6KA3, GNG5, RPS6KA2, STOM, GNAQNAPGNSF, ELAVL1, APP, LSM6, MTR, FN1, RAB11FIP5, TUBG1, VTI1B, STX6, STX7, STX12, AKAP11, NAPA, SCFD2, PRKACB, PRKAR1B, VAMP4, STX8, NBAS, PIPOX, FBXW7, STXBP6, FMN1, CPNE5, SEC22B, PRPSAP2, UFSP2, FAM177A1, SPRTN


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 SPRED2_NAPG


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 SPRED2_NAPG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSPRED2C0003873Rheumatoid Arthritis2CTD_human
TgeneNAPGC0005586Bipolar Disorder3PSYGENET