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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:GNG5-NMI (FusionGDB2 ID:33640)

Fusion Gene Summary for GNG5-NMI

check button Fusion gene summary
Fusion gene informationFusion gene name: GNG5-NMI
Fusion gene ID: 33640
HgeneTgene
Gene symbol

GNG5

NMI

Gene ID

2787

9111

Gene nameG protein subunit gamma 5N-myc and STAT interactor
Synonyms--
Cytomap

1p22.3

2q23.3

Type of geneprotein-codingprotein-coding
Descriptionguanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5guanine nucleotide binding protein (G protein), gamma 5N-myc-interactor
Modification date2020031320200313
UniProtAcc

P63218

Q13287

Ensembl transtripts involved in fusion geneENST00000487806, ENST00000370645, 
ENST00000370641, 
ENST00000243346, 
Fusion gene scores* DoF score5 X 4 X 4=806 X 4 X 5=120
# samples 56
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GNG5 [Title/Abstract] AND NMI [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGNG5(84971693)-NMI(152127389), # samples:1
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

check buttonFusion gene breakpoints across GNG5 (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 NMI (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
ChimerDB4COADTCGA-DM-A1HBGNG5chr1

84971693

-NMIchr2

152127389

-


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Fusion Gene ORF analysis for GNG5-NMI

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-3CDSENST00000487806ENST00000243346GNG5chr1

84971693

-NMIchr2

152127389

-
In-frameENST00000370645ENST00000243346GNG5chr1

84971693

-NMIchr2

152127389

-
In-frameENST00000370641ENST00000243346GNG5chr1

84971693

-NMIchr2

152127389

-

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)
ENST00000370645GNG5chr184971693-ENST00000243346NMIchr2152127389-832421265603112
ENST00000370641GNG5chr184971693-ENST00000243346NMIchr2152127389-966555521153122

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
ENST00000370645ENST00000243346GNG5chr184971693-NMIchr2152127389-0.175657060.82434297
ENST00000370641ENST00000243346GNG5chr184971693-NMIchr2152127389-0.280232580.71976745

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Fusion Genomic Features for GNG5-NMI


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 GNG5-NMI


check button Go to

FGviewer for the breakpoints of chr1:84971693-chr2:152127389

.
- 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
GNG5

P63218

NMI

Q13287

FUNCTION: Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction.FUNCTION: Acts as a signaling pathway regulator involved in innate immune system response (PubMed:9989503, PubMed:26342464, PubMed:29038465, PubMed:29350881). In response to interleukin 2/IL2 and interferon IFN-gamma/IFNG, interacts with signal transducer and activator of transcription/STAT which activate the transcription of downstream genes involved in a multitude of signals for development and homeostasis (PubMed:9989503). Enhances the recruitment of CBP/p300 coactivators to STAT1 and STAT5, resulting in increased STAT1- and STAT5-dependent transcription (PubMed:9989503). In response to interferon IFN-alpha, associates in a complex with signaling pathway regulator IFI35 to regulate immune response; the complex formation prevents proteasome-mediated degradation of IFI35 (PubMed:10779520, PubMed:10950963). In complex with IFI35, inhibits virus-triggered type I IFN-beta production when ubiquitinated by ubiquitin-protein ligase TRIM21 (PubMed:26342464). In complex with IFI35, negatively regulates nuclear factor NF-kappa-B signaling by inhibiting the nuclear translocation, activation and transcription of NF-kappa-B subunit p65/RELA, resulting in the inhibition of endothelial cell proliferation, migration and re-endothelialization of injured arteries (PubMed:29350881). Negatively regulates virus-triggered type I interferon/IFN production by inducing proteosome-dependent degradation of IRF7, a transcriptional regulator of type I IFN, thereby interfering with cellular antiviral responses (By similarity). Beside its role as an intracellular signaling pathway regulator, also functions extracellularly as damage-associated molecular patterns (DAMPs) to promote inflammation, when actively released by macrophage to the extracellular space during cell injury or pathogen invasion (PubMed:29038465). Macrophage-secreted NMI activates NF-kappa-B signaling in adjacent macrophages through Toll-like receptor 4/TLR4 binding and activation, thereby inducing NF-kappa-B translocation from the cytoplasm into the nucleus which promotes the release of proinflammatory cytokines (PubMed:29038465). {ECO:0000250|UniProtKB:O35309, ECO:0000269|PubMed:10779520, ECO:0000269|PubMed:10950963, ECO:0000269|PubMed:26342464, ECO:0000269|PubMed:29038465, ECO:0000269|PubMed:29350881, ECO:0000269|PubMed:9989503}.

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
TgeneNMIchr1:84971693chr2:152127389ENST000002433466830_64247.0308.0Coiled coilOntology_term=ECO:0000255
TgeneNMIchr1:84971693chr2:152127389ENST0000024334668103_192247.0308.0DomainNID 1
TgeneNMIchr1:84971693chr2:152127389ENST0000024334668201_292247.0308.0DomainNID 2


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Fusion Gene Sequence for GNG5-NMI


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.
>In-frame_ENST00000370645_ENST00000243346_TCGA-DM-A1HB_GNG5_chr1_84971693_-_NMI_chr2_152127389_length(transcript)=832nt_BP=421nt
CTTCCCACAAACTGGGAGGAAAACTGAGACCTCCTGGTCACCCGCCGCCGGGCCTTTTAGAAACTCCCACAAGCTCTGCCTTCCCTCCCT
GGTCCTCTTCAGACCCCCTCTTAGTTCTTCGCGGCTAACGGCTCGCGCTCGGGGCCGGGTGTGGAGCTGGAACAGAGGGCTGGCAAGGCG
CGCATGCGCACCGAGGGTGGAGCCGCTGAGCACAGAACCGGAAACTTAGAGACAAAGTTCGGAGCCCCGCCCCCGCCGCGCGCCGCTGAG
TTGTCTGGCCCCGCCGACCCACGGCCCACGACCCACCGACCCACGAATCGGCCCGGCCGTCGCGTGCACCATGTCTGGCTCCTCCAGCGT
CGCCGCTATGAAGAAAGTGGTTCAACAGCTCCGGCTGGAGGCCGGACTCAACCGCGTAAAAATATTTTCAGGAACATCTAAGAGGACAGT
GCTTCTGACAGGAATGGAAGGCATTCAAATGGATGAAGAAATTGTGGAGGATTTAATTAACATTCACTTTCAACGGGCAAAGAATGGAGG
TGGAGAAGTAGATGTGGTCAAGTGTTCTCTAGGTCAACCTCACATAGCATACTTTGAAGAATAGACTTAACAGAATCATGAAAACTATAG
CTTTTTAACCCGGATTACTGTAAATGTTTGACAAAAATGAATATGCTTTTCCTTAAAAAATGAAAACTTTAATTTTTACCATCCATTTAT
GTTTAGATACAAAACTTATTTCCATGTTTCTGAATCTTCTTTGTTTCAAATGGTGCTGCATGTTTTCAACTACAATAAGTGCACTGTAAT

>In-frame_ENST00000370645_ENST00000243346_TCGA-DM-A1HB_GNG5_chr1_84971693_-_NMI_chr2_152127389_length(amino acids)=112AA_start in transcript=265_stop in transcript=603
MSCLAPPTHGPRPTDPRIGPAVACTMSGSSSVAAMKKVVQQLRLEAGLNRVKIFSGTSKRTVLLTGMEGIQMDEEIVEDLINIHFQRAKN

--------------------------------------------------------------
>In-frame_ENST00000370641_ENST00000243346_TCGA-DM-A1HB_GNG5_chr1_84971693_-_NMI_chr2_152127389_length(transcript)=966nt_BP=555nt
CTTCCCACAAACTGGGAGGAAAACTGAGACCTCCTGGTCACCCGCCGCCGGGCCTTTTAGAAACTCCCACAAGCTCTGCCTTCCCTCCCT
GGTCCTCTTCAGACCCCCTCTTAGTTCTTCGCGGCTAACGGTAAGCTCTCTCCTTACCTCTCCCTAATCGGCCCCTCTGGAGAGGAAAAG
AAAACTTAAGAGTCGGGTCGCGCTAGCCTCCAGCAGCCGCCGCGCCCACCGACTGCTCCGCCCCTTCTCCTCCCCCTCCTCCAGGCTCGC
GCTCGGGGCCGGGTGTGGAGCTGGAACAGAGGGCTGGCAAGGCGCGCATGCGCACCGAGGGTGGAGCCGCTGAGCACAGAACCGGAAACT
TAGAGACAAAGTTCGGAGCCCCGCCCCCGCCGCGCGCCGCTGAGTTGTCTGGCCCCGCCGACCCACGGCCCACGACCCACCGACCCACGA
ATCGGCCCGGCCGTCGCGTGCACCATGTCTGGCTCCTCCAGCGTCGCCGCTATGAAGAAAGTGGTTCAACAGCTCCGGCTGGAGGCCGGA
CTCAACCGCGTAAAAATATTTTCAGGAACATCTAAGAGGACAGTGCTTCTGACAGGAATGGAAGGCATTCAAATGGATGAAGAAATTGTG
GAGGATTTAATTAACATTCACTTTCAACGGGCAAAGAATGGAGGTGGAGAAGTAGATGTGGTCAAGTGTTCTCTAGGTCAACCTCACATA
GCATACTTTGAAGAATAGACTTAACAGAATCATGAAAACTATAGCTTTTTAACCCGGATTACTGTAAATGTTTGACAAAAATGAATATGC
TTTTCCTTAAAAAATGAAAACTTTAATTTTTACCATCCATTTATGTTTAGATACAAAACTTATTTCCATGTTTCTGAATCTTCTTTGTTT

>In-frame_ENST00000370641_ENST00000243346_TCGA-DM-A1HB_GNG5_chr1_84971693_-_NMI_chr2_152127389_length(amino acids)=122AA_start in transcript=521_stop in transcript=153
MLNHFLHSGDAGGARHGARDGRADSWVGGSWAVGRRGQTTQRRAAGAGLRTLSLSFRFCAQRLHPRCACAPCQPSVPAPHPAPSASLEEG

--------------------------------------------------------------

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Fusion Gene PPI Analysis for GNG5-NMI


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 GNG5-NMI


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 GNG5-NMI


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGNG5C0033578Prostatic Neoplasms1CTD_human
HgeneGNG5C0376358Malignant neoplasm of prostate1CTD_human
TgeneNMIC0023893Liver Cirrhosis, Experimental1CTD_human