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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: 24359

FusionGeneSummary for NINL_GINS1

check button Fusion gene summary
Fusion gene informationFusion gene name: NINL_GINS1
Fusion gene ID: 24359
HgeneTgene
Gene symbol

NINL

GINS1

Gene ID

22981

9837

Gene nameninein likeGINS complex subunit 1
SynonymsNLPIMD55|PSF1
Cytomap

20p11.21

20p11.21

Type of geneprotein-codingprotein-coding
Descriptionninein-like proteinDNA replication complex GINS protein PSF1GINS complex subunit 1 (Psf1 homolog)partner of sld five-1
Modification date2018052320180523
UniProtAcc

Q9Y2I6

Q14691

Ensembl transtripts involved in fusion geneENST00000278886, ENST00000422516, 
ENST00000464285, 
ENST00000262460, 
ENST00000429262, ENST00000484893, 
Fusion gene scores* DoF score5 X 4 X 5=1003 X 2 X 3=18
# samples 53
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: NINL [Title/Abstract] AND GINS1 [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
TCGARVLUSCTCGA-77-7465-01ANINLchr20

25507044

-GINS1chr20

25397740

+
* 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-shiftENST00000278886ENST00000262460NINLchr20

25507044

-GINS1chr20

25397740

+
Frame-shiftENST00000278886ENST00000429262NINLchr20

25507044

-GINS1chr20

25397740

+
5CDS-3UTRENST00000278886ENST00000484893NINLchr20

25507044

-GINS1chr20

25397740

+
Frame-shiftENST00000422516ENST00000262460NINLchr20

25507044

-GINS1chr20

25397740

+
Frame-shiftENST00000422516ENST00000429262NINLchr20

25507044

-GINS1chr20

25397740

+
5CDS-3UTRENST00000422516ENST00000484893NINLchr20

25507044

-GINS1chr20

25397740

+
intron-3CDSENST00000464285ENST00000262460NINLchr20

25507044

-GINS1chr20

25397740

+
intron-3CDSENST00000464285ENST00000429262NINLchr20

25507044

-GINS1chr20

25397740

+
intron-3UTRENST00000464285ENST00000484893NINLchr20

25507044

-GINS1chr20

25397740

+

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FusionProtFeatures for NINL_GINS1


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

Q9Y2I6

GINS1

Q14691

Involved in the microtubule organization in interphasecells. Overexpression induces the fragmentation of the Golgi, andcauses lysosomes to disperse toward the cell periphery; it alsointerferes with mitotic spindle assembly. May play a role inovarian carcinogenesis. {ECO:0000269|PubMed:12852856,ECO:0000269|PubMed:16254247, ECO:0000269|PubMed:18538832}. The GINS complex plays an essential role in theinitiation of DNA replication, and progression of DNA replicationforks. GINS complex seems to bind preferentially to single-stranded DNA. GINS1 is essential for function.{ECO:0000269|PubMed:17417653}.

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 NINL_GINS1


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 NINL_GINS1


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
NINLSPERT, TCEB3, CCDC33, MAD1L1, AKAP17A, UTP14A, ZNF646, GPKOW, LZTS2, ZFC3H1, KANSL1, DCTN5, SH3BP5L, TSPYL4, JUNB, ZNF426, ZFHX3, CLEC1B, SYT17, RIBC2, KAT7, GCC1, RGS2, CCDC130, APEX2, EWSR1, MCM10, ZNF250, TCEANC, RCOR3, TNNT1, MBIP, FAM107A, EZH2, LRSAM1, ANAPC2, CDC27, CDC20, FZR1, BRCA1, TUBG1, TUBGCP4, PLK1, LATS2, CEP250, KAT5, CCHCR1, RBM41, CCDC146, SH2D4A, FAM161A, L3MBTL4, HAUS1, ZNF417, LRRC39, CEP128, ABLIM1, ALDH3A2, ARHGAP21, ARRB2, CEP131, C1orf198, CC2D1A, CCDC138, CCDC14, CCDC66, CCDC85C, CCP110, CEP162, CEP350, CEP55, CEP85, CEP97, CKAP2, CNOT1, CSPP1, DYNC1H1, DYNC1LI2, FGFR1OP, GPATCH1, GPS2, IFT74, IFT81, KANK2, GSE1, KIAA1671, KIF14, KIF1B, ERVK3-1, LPP, LUZP1, MAP7D3, MPHOSPH9, MZT2A, NCKAP5L, NCOR1, NEDD1, NME7, OFD1, PALLD, PDLIM7, PPP1R13B, PRRC2B, SCYL2, SDCCAG3, SIPA1L3, SVIL, TCHP, TNRC6A, TNRC6B, TP53, TP53BP2, TROAP, TTK, TXLNA, TXLNG, WDR83, ZNF598, ANKHD1-EIF4EBP3, BCR, PROSER3, CAMK2B, CAMSAP1, CAMSAP2, CAMSAP3, CCDC112, CCDC22, CCDC77, CEP170, CEP192, CEP89, CEP95, CKAP5, CNOT10, CNOT3, COMMD2, CRKL, CYLD, DAPK3, DCAF7, DCP1B, DHX35, DIAPH3, DLG5, DNMBP, DSP, DYNC1LI1, EIF4ENIF1, ERC1, FAM83H, GIGYF1, GIGYF2, GTSE1, HAUS2, HAUS5, HAUS6, HAUS7, HDAC3, HSPA1B, HSPA1L, ITSN2, CEP170B, KIAA0753, KIAA1217, CEP295, KIF7, LATS1, LMO7, MICAL3, MIS18A, MIS18BP1, MPP5, MTUS1, NDEL1, PCM1, PDZD11, PIK3C2A, PLEKHA7, PLEKHG1, PPP1CA, PTPN13, RASSF8, RAVER1, RCOR1, RPGRIP1L, RQCD1, SASS6, SH3RF1, SHKBP1, SIPA1L1, SIPA1L2, SMG7, TANC1, TBK1, TBL1XR1, TDRD3, TNIP1, TTC28, TTF2, TUBGCP2, USP54, VPS45, XRN1, RBSN, CENPJ, LZTS3, GAN, ZNF408, CCDC172, MRPS34, NKAP, TPM2, CAMK2A, DCTN2, AHI1, DCTN1GINS1GINS4, GINS3, GINS2, MRE11A, TOPBP1, TIPIN, CSNK1G2, GTF2E2, CCDC84, MCM7


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 NINL_GINS1


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 NINL_GINS1


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