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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: 23985

FusionGeneSummary for NEFM_NOL4

check button Fusion gene summary
Fusion gene informationFusion gene name: NEFM_NOL4
Fusion gene ID: 23985
HgeneTgene
Gene symbol

NEFM

NOL4

Gene ID

4741

8715

Gene nameneurofilament mediumnucleolar protein 4
SynonymsNEF3|NF-M|NFMCT125|HRIHFB2255|NOLP
Cytomap

8p21.2

18q12.1

Type of geneprotein-codingprotein-coding
Descriptionneurofilament medium polypeptide160 kDa neurofilament proteinneurofilament 3neurofilament triplet M proteinneurofilament, medium polypeptide 150kDaneurofilament-3 (150 kD medium)nucleolar protein 4cancer/testis antigen 125nucleolar localized protein
Modification date2018051920180519
UniProtAcc

P07197

O94818

Ensembl transtripts involved in fusion geneENST00000221166, ENST00000518131, 
ENST00000521540, ENST00000437366, 
ENST00000433454, 
ENST00000261592, 
ENST00000269185, ENST00000535384, 
ENST00000535475, ENST00000589544, 
ENST00000538587, ENST00000590846, 
Fusion gene scores* DoF score2 X 2 X 1=44 X 4 X 4=64
# samples 24
** MAII scorelog2(2/4*10)=2.32192809488736log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NEFM [Title/Abstract] AND NOL4 [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
ChiTaRS3.1BX489207NEFMchr8

24776294

-NOL4chr18

31655782

+
* 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
3UTR-intronENST00000221166ENST00000261592NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000269185NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000535384NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000535475NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000589544NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000538587NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000221166ENST00000590846NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000261592NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000269185NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000535384NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000535475NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000589544NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000538587NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000518131ENST00000590846NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000261592NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000269185NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000535384NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000535475NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000589544NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000538587NEFMchr8

24776294

-NOL4chr18

31655782

+
intron-intronENST00000521540ENST00000590846NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000261592NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000269185NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000535384NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000535475NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000589544NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000538587NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000437366ENST00000590846NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000261592NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000269185NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000535384NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000535475NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000589544NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000538587NEFMchr8

24776294

-NOL4chr18

31655782

+
3UTR-intronENST00000433454ENST00000590846NEFMchr8

24776294

-NOL4chr18

31655782

+

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FusionProtFeatures for NEFM_NOL4


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

P07197

NOL4

O94818

Neurofilaments usually contain three intermediatefilament proteins: L, M, and H which are involved in themaintenance of neuronal caliber.

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 NEFM_NOL4


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 NEFM_NOL4


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 NEFM_NOL4


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 NEFM_NOL4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNEFMC0005586Bipolar Disorder1PSYGENET
HgeneNEFMC0011570Mental Depression1PSYGENET
HgeneNEFMC0011581Depressive disorder1PSYGENET
HgeneNEFMC0014175Endometriosis1CTD_human