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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: 23992

FusionGeneSummary for NEGR1_ZRANB2

check button Fusion gene summary
Fusion gene informationFusion gene name: NEGR1_ZRANB2
Fusion gene ID: 23992
HgeneTgene
Gene symbol

NEGR1

ZRANB2

Gene ID

257194

9406

Gene nameneuronal growth regulator 1zinc finger RANBP2-type containing 2
SynonymsDMML2433|IGLON4|KILON|NtraZIS|ZIS1|ZIS2|ZNF265
Cytomap

1p31.1

1p31.1

Type of geneprotein-codingprotein-coding
Descriptionneuronal growth regulator 1IgLON family member 4a kindred of IgLONneurotractinzinc finger Ran-binding domain-containing protein 2zinc finger protein 265zinc finger, RAN-binding domain containing 2zinc-finger, splicing
Modification date2018052220180522
UniProtAcc

Q7Z3B1

O95218

Ensembl transtripts involved in fusion geneENST00000357731, ENST00000306821, 
ENST00000434200, ENST00000467479, 
ENST00000370920, ENST00000477096, 
ENST00000254821, 
Fusion gene scores* DoF score7 X 3 X 6=1261 X 1 X 1=1
# samples 71
** MAII scorelog2(7/126*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: NEGR1 [Title/Abstract] AND ZRANB2 [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
TCGALDGBMTCGA-41-5651-01ANEGR1chr1

72748002

-ZRANB2chr1

71544391

-
* 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-shiftENST00000357731ENST00000370920NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
5CDS-intronENST00000357731ENST00000477096NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
5CDS-intronENST00000357731ENST00000254821NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-3CDSENST00000306821ENST00000370920NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-intronENST00000306821ENST00000477096NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-intronENST00000306821ENST00000254821NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
Frame-shiftENST00000434200ENST00000370920NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
5CDS-intronENST00000434200ENST00000477096NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
5CDS-intronENST00000434200ENST00000254821NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-3CDSENST00000467479ENST00000370920NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-intronENST00000467479ENST00000477096NEGR1chr1

72748002

-ZRANB2chr1

71544391

-
intron-intronENST00000467479ENST00000254821NEGR1chr1

72748002

-ZRANB2chr1

71544391

-

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FusionProtFeatures for NEGR1_ZRANB2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NEGR1

Q7Z3B1

ZRANB2

O95218

May be involved in cell-adhesion. May function as atrans-neural growth-promoting factor in regenerative axonsprouting in the mammalian brain (By similarity). {ECO:0000250}. Splice factor required for alternative splicing ofTRA2B/SFRS10 transcripts. May interfere with constitutive 5'-splice site selection. {ECO:0000269|PubMed:11448987}.

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 NEGR1_ZRANB2


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 NEGR1_ZRANB2


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
NEGR1NTM, LSAMP, NEGR1ZRANB2ARRB1, U2AF1, SNRNP70, TRA2B, USP39, EMD, SREK1, HDGF, ARRB2, CUL3, SRXN1, ATP6V1F, AHCYL1, USP34, STAM, SSSCA1, PCMT1, PSMA1, UBQLN2, UBQLN1, UBL7, TTC1, UBA52, TYMS, UBXN7, TTLL12, UBE2V2, UNK, UBE2B, UBE2C, UBE4B, SRSF7, UCHL3, TTC9C, SULT1A1, ZNF644, NUBP2, SMURF1, CSNK2A1, KIF20A, FBXL7, SRPK2, SRPK1, CORO1B, PARVA, SWAP70, TBC1D17, C18orf25, CDK1, OSBP, ARL6IP4, SERPINB5, TOP1, PRPF4B, LUC7L2, LUC7L, KPNA5, RPL26L1, RSBN1L, RSBN1, LUC7L3, VANGL1, PIP4K2C, PIP4K2B, PIP4K2A, SRSF11, PLD1, ACTL6A, NFKBIL1, EPB41L3, EWSR1, TIGD6, RC3H1, EPB41L2, U2AF2, GTF2E2, SYNCRIP, WDR60


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 NEGR1_ZRANB2


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 NEGR1_ZRANB2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNEGR1C0028754Obesity1CTD_human