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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:NALCN-GRM5 (FusionGDB2 ID:57158)

Fusion Gene Summary for NALCN-GRM5

check button Fusion gene summary
Fusion gene informationFusion gene name: NALCN-GRM5
Fusion gene ID: 57158
HgeneTgene
Gene symbol

NALCN

GRM5

Gene ID

259232

2915

Gene namesodium leak channel, non-selectiveglutamate metabotropic receptor 5
SynonymsCLIFAHDD|CanIon|IHPRF|IHPRF1|INNFD|VGCNL1|bA430M15.1GPRC1E|MGLUR5|PPP1R86|mGlu5
Cytomap

13q32.3-q33.1

11q14.2-q14.3

Type of geneprotein-codingprotein-coding
Descriptionsodium leak channel non-selective proteinfour repeat voltage-gated ion channelvoltage gated channel like 1metabotropic glutamate receptor 5glutamate receptor, metabotropic 5protein phosphatase 1, regulatory subunit 86
Modification date2020031320200329
UniProtAcc

Q8IZF0

P41594

Ensembl transtripts involved in fusion geneENST00000251127, ENST00000376196, 
ENST00000376200, ENST00000470333, 
ENST00000305432, ENST00000305447, 
ENST00000393294, ENST00000393297, 
ENST00000418177, ENST00000455756, 
Fusion gene scores* DoF score4 X 4 X 1=167 X 5 X 4=140
# samples 47
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NALCN [Title/Abstract] AND GRM5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNALCN(101960103)-GRM5(88279241), # 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 NALCN (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 GRM5 (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
ChiTaRS5.0N/AFN090508NALCNchr13

101960103

+GRM5chr11

88279241

+


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Fusion Gene ORF analysis for NALCN-GRM5

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-intronENST00000251127ENST00000305432NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000251127ENST00000305447NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000251127ENST00000393294NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000251127ENST00000393297NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000251127ENST00000418177NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000251127ENST00000455756NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000305432NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000305447NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000393294NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000393297NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000418177NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376196ENST00000455756NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000305432NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000305447NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000393294NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000393297NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000418177NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000376200ENST00000455756NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000305432NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000305447NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000393294NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000393297NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000418177NALCNchr13

101960103

+GRM5chr11

88279241

+
intron-intronENST00000470333ENST00000455756NALCNchr13

101960103

+GRM5chr11

88279241

+

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 NALCN-GRM5


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 NALCN-GRM5


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:101960103/:88279241)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

Q8IZF0

GRM5

P41594

FUNCTION: Voltage-independent, cation-nonselective channel which is permeable to sodium, potassium and calcium ions. Regulates the resting membrane potential and controls neuronal excitability (PubMed:17448995). Neuropeptides such as neurotensin and substance P (SP) stimulate the firing of action potentials by activating NALCN through a SRC family kinases-dependent pathway. In addition to its baseline activity, NALCN activity is enhanced/modulated by several GPCRs. Required for normal respiratory rhythm and neonatal survival. Involved in systemic osmoregulation by controlling the serum sodium concentration. NALCN is partly responsible for the substance P-induced depolarization and regulation of the intestinal pace-making activity in the interstitial cells of Cajal. Plays a critical role in both maintenance of spontaneous firing of substantia nigra pars reticulata (SNr) neurons and physiological modulation of SNr neuron excitability (By similarity). {ECO:0000250|UniProtKB:Q8BXR5, ECO:0000269|PubMed:17448995}.FUNCTION: G-protein coupled receptor for glutamate. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Signaling activates a phosphatidylinositol-calcium second messenger system and generates a calcium-activated chloride current. Plays an important role in the regulation of synaptic plasticity and the modulation of the neural network activity. {ECO:0000269|PubMed:25042998, ECO:0000269|PubMed:7908515}.

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 NALCN-GRM5


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 NALCN-GRM5


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 NALCN-GRM5


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 NALCN-GRM5


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