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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:KIAA1211-NMU (FusionGDB2 ID:42070)

Fusion Gene Summary for KIAA1211-NMU

check button Fusion gene summary
Fusion gene informationFusion gene name: KIAA1211-NMU
Fusion gene ID: 42070
HgeneTgene
Gene symbol

KIAA1211

NMU

Gene ID

57482

10874

Gene namecapping protein inhibiting regulator of actin dynamicsneuromedin U
SynonymsCRAD|KIAA1211-
Cytomap

4q12

4q12

Type of geneprotein-codingprotein-coding
Descriptioncancer-related regulator of actin dynamicsneuromedin-Uneuromedin U precursor-related peptide/neuromedin U preproproteinprepro-NMU
Modification date2020031320200313
UniProtAcc.

Q9HB89

Ensembl transtripts involved in fusion geneENST00000264229, ENST00000541073, 
ENST00000504228, ENST00000505410, 
ENST00000511469, ENST00000264218, 
ENST00000505262, ENST00000507338, 
ENST00000515325, 
Fusion gene scores* DoF score8 X 3 X 5=1206 X 4 X 7=168
# samples 77
** MAII scorelog2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KIAA1211 [Title/Abstract] AND NMU [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKIAA1211(57045596)-NMU(56496627), # samples:4
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneKIAA1211

GO:0030838

positive regulation of actin filament polymerization

30361697

HgeneKIAA1211

GO:2000813

negative regulation of barbed-end actin filament capping

30361697

TgeneNMU

GO:0007218

neuropeptide signaling pathway

10894543|11027493


check buttonFusion gene breakpoints across KIAA1211 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across NMU (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4GBMTCGA-06-2559-01AKIAA1211chr4

57045596

+NMUchr4

56496627

-
ChimerDB4GBMTCGA-06-2559KIAA1211chr4

57045596

+NMUchr4

56496627

-
ChimerDB4GBMTCGA-06-2559-01AKIAA1211chr4

57045596

+NMUchr4

56496627

-
ChimerDB4GBMTCGA-06-2559-01AKIAA1211chr4

57045596

-NMUchr4

56496627

-


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Fusion Gene ORF analysis for KIAA1211-NMU

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
5UTR-3CDSENST00000264229ENST00000511469KIAA1211chr4

57045596

+NMUchr4

56496627

-
5UTR-3CDSENST00000264229ENST00000264218KIAA1211chr4

57045596

+NMUchr4

56496627

-
5UTR-3CDSENST00000264229ENST00000505262KIAA1211chr4

57045596

+NMUchr4

56496627

-
5UTR-3CDSENST00000264229ENST00000507338KIAA1211chr4

57045596

+NMUchr4

56496627

-
5UTR-5UTRENST00000264229ENST00000515325KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000541073ENST00000511469KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000541073ENST00000264218KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000541073ENST00000505262KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000541073ENST00000507338KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-5UTRENST00000541073ENST00000515325KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000504228ENST00000511469KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000504228ENST00000264218KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000504228ENST00000505262KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000504228ENST00000507338KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-5UTRENST00000504228ENST00000515325KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000505410ENST00000511469KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000505410ENST00000264218KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000505410ENST00000505262KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-3CDSENST00000505410ENST00000507338KIAA1211chr4

57045596

+NMUchr4

56496627

-
intron-5UTRENST00000505410ENST00000515325KIAA1211chr4

57045596

+NMUchr4

56496627

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for KIAA1211-NMU


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for KIAA1211-NMU


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

Q9HB89

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Receptor for the neuromedin-U and neuromedin-S neuropeptides. {ECO:0000250, ECO:0000269|PubMed:10899166}.

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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Fusion Gene Sequence for KIAA1211-NMU


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for KIAA1211-NMU


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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Related Drugs for KIAA1211-NMU


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for KIAA1211-NMU


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