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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: 23494

FusionGeneSummary for NBEAL1_MEN1

check button Fusion gene summary
Fusion gene informationFusion gene name: NBEAL1_MEN1
Fusion gene ID: 23494
HgeneTgene
Gene symbol

NBEAL1

MEN1

Gene ID

65065

4221

Gene nameneurobeachin like 1menin 1
SynonymsA530083I02Rik|ALS2CR16|ALS2CR17MEAI|SCG2
Cytomap

2q33.2

11q13.1

Type of geneprotein-codingprotein-coding
Descriptionneurobeachin-like protein 1amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 16amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 17amyotrophic lateral sclerosis 2 chromosomal region candidate gene 16 proteinmenin
Modification date2018051920180523
UniProtAcc

Q6ZS30

O00255

Ensembl transtripts involved in fusion geneENST00000449802, ENST00000478884, 
ENST00000377316, ENST00000377321, 
ENST00000377326, ENST00000312049, 
ENST00000315422, ENST00000443283, 
ENST00000394374, ENST00000337652, 
ENST00000394376, ENST00000377313, 
ENST00000478548, 
Fusion gene scores* DoF score5 X 5 X 5=1252 X 2 X 2=8
# samples 62
** MAII scorelog2(6/125*10)=-1.05889368905357
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: NBEAL1 [Title/Abstract] AND MEN1 [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
TgeneMEN1

GO:0000122

negative regulation of transcription by RNA polymerase II

9989505|12837246|23784080

TgeneMEN1

GO:0000165

MAPK cascade

12226747

TgeneMEN1

GO:0001933

negative regulation of protein phosphorylation

12226747

TgeneMEN1

GO:0006974

cellular response to DNA damage stimulus

16690369

TgeneMEN1

GO:0008285

negative regulation of cell proliferation

15331604

TgeneMEN1

GO:0009411

response to UV

16690369

TgeneMEN1

GO:0010332

response to gamma radiation

12874027

TgeneMEN1

GO:0032092

positive regulation of protein binding

20484083

TgeneMEN1

GO:0043433

negative regulation of DNA binding transcription factor activity

11526476|12226747

TgeneMEN1

GO:0045786

negative regulation of cell cycle

15331604

TgeneMEN1

GO:0045892

negative regulation of transcription, DNA-templated

12226747

TgeneMEN1

GO:0046329

negative regulation of JNK cascade

12226747


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
ChiTaRS3.1BC001802NBEAL1chr2

204055448

-MEN1chr11

64572533

-
* 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-intronENST00000449802ENST00000377316NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000377321NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000377326NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000312049NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000315422NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000443283NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000394374NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000337652NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000394376NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000449802ENST00000377313NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-5UTRENST00000449802ENST00000478548NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000377316NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000377321NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000377326NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000312049NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000315422NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000443283NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000394374NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000337652NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000394376NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-intronENST00000478884ENST00000377313NBEAL1chr2

204055448

-MEN1chr11

64572533

-
intron-5UTRENST00000478884ENST00000478548NBEAL1chr2

204055448

-MEN1chr11

64572533

-

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FusionProtFeatures for NBEAL1_MEN1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NBEAL1

Q6ZS30

MEN1

O00255


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 NBEAL1_MEN1


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 NBEAL1_MEN1


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 NBEAL1_MEN1


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 NBEAL1_MEN1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMEN1C0025267Multiple Endocrine Neoplasia Type 138CTD_human;ORPHANET;UNIPROT
TgeneMEN1C1840402HYPERPARATHYROIDISM 16CTD_human;ORPHANET;UNIPROT
TgeneMEN1C0030297Pancreatic Neoplasm2CTD_human
TgeneMEN1C0011993Vipoma1CTD_human
TgeneMEN1C0017150Gastrinoma1CTD_human
TgeneMEN1C0017689Glucagonoma1CTD_human;HPO
TgeneMEN1C0021670insulinoma1CTD_human;HPO;ORPHANET
TgeneMEN1C0206686Adrenocortical carcinoma1CTD_human
TgeneMEN1C0206754Neuroendocrine Tumors1CTD_human