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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:DNAH12-GLRA1 (FusionGDB2 ID:23334)

Fusion Gene Summary for DNAH12-GLRA1

check button Fusion gene summary
Fusion gene informationFusion gene name: DNAH12-GLRA1
Fusion gene ID: 23334
HgeneTgene
Gene symbol

DNAH12

GLRA1

Gene ID

201625

2741

Gene namedynein axonemal heavy chain 12glycine receptor alpha 1
SynonymsDHC3|DLP12|DLP3|DNAH12L|DNAH7L|DNAHC12|DNAHC3|DNHD2|HDHC3|HL-19|HL19HKPX1|STHE
Cytomap

3p14.3

5q33.1

Type of geneprotein-codingprotein-coding
Descriptiondynein heavy chain 12, axonemalaxonemal beta dynein heavy chain 12axonemal dynein heavy chain isotype3ciliary dynein heavy chain 12dynein heavy chain domain-containing protein 2dynein, axonemal, heavy polypeptide 12dynein, heavy chain-5glycine receptor subunit alpha-1glycine receptor 48 kDa subunitglycine receptor strychnine-binding subunit
Modification date2020032020200313
UniProtAcc

Q6ZR08

P23415

Ensembl transtripts involved in fusion geneENST00000311202, ENST00000344804, 
ENST00000351747, ENST00000389536, 
ENST00000462713, 
ENST00000274576, 
ENST00000455880, ENST00000471351, 
ENST00000545569, 
Fusion gene scores* DoF score5 X 5 X 2=502 X 3 X 2=12
# samples 53
** MAII scorelog2(5/50*10)=0log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: DNAH12 [Title/Abstract] AND GLRA1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDNAH12(57421826)-GLRA1(151224279), # 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
TgeneGLRA1

GO:0006811

ion transport

2155780

TgeneGLRA1

GO:0006821

chloride transport

8137830

TgeneGLRA1

GO:0007218

neuropeptide signaling pathway

2155780

TgeneGLRA1

GO:0071230

cellular response to amino acid stimulus

16144831

TgeneGLRA1

GO:0071294

cellular response to zinc ion

16144831

TgeneGLRA1

GO:0071361

cellular response to ethanol

25973519

TgeneGLRA1

GO:1902476

chloride transmembrane transport

16144831


check buttonFusion gene breakpoints across DNAH12 (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 GLRA1 (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/AFN069987DNAH12chr3

57421826

+GLRA1chr5

151224279

+


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Fusion Gene ORF analysis for DNAH12-GLRA1

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-intronENST00000311202ENST00000274576DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000311202ENST00000455880DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000311202ENST00000471351DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000311202ENST00000545569DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000344804ENST00000274576DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000344804ENST00000455880DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000344804ENST00000471351DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000344804ENST00000545569DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000351747ENST00000274576DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000351747ENST00000455880DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000351747ENST00000471351DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000351747ENST00000545569DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000389536ENST00000274576DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000389536ENST00000455880DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000389536ENST00000471351DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000389536ENST00000545569DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000462713ENST00000274576DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000462713ENST00000455880DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000462713ENST00000471351DNAH12chr3

57421826

+GLRA1chr5

151224279

+
intron-intronENST00000462713ENST00000545569DNAH12chr3

57421826

+GLRA1chr5

151224279

+

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 DNAH12-GLRA1


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 DNAH12-GLRA1


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/:57421826/:151224279)
- 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
DNAH12

Q6ZR08

GLRA1

P23415

FUNCTION: Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly (By similarity). {ECO:0000250}.FUNCTION: Glycine receptors are ligand-gated chloride channels (PubMed:23994010, PubMed:25730860). Channel opening is triggered by extracellular glycine (PubMed:2155780, PubMed:7920629, PubMed:14551753, PubMed:16144831, PubMed:22715885, PubMed:22973015, PubMed:25973519, PubMed:9009272). Channel opening is also triggered by taurine and beta-alanine (PubMed:16144831, PubMed:9009272). Channel characteristics depend on the subunit composition; heteropentameric channels are activated by lower glycine levels and display faster desensitization (PubMed:14551753). Plays an important role in the down-regulation of neuronal excitability (PubMed:8298642, PubMed:9009272). Contributes to the generation of inhibitory postsynaptic currents (PubMed:25445488). Channel activity is potentiated by ethanol (PubMed:25973519). Potentiation of channel activity by intoxicating levels of ethanol contribute to the sedative effects of ethanol (By similarity). {ECO:0000250|UniProtKB:Q64018, ECO:0000269|PubMed:14551753, ECO:0000269|PubMed:16144831, ECO:0000269|PubMed:2155780, ECO:0000269|PubMed:22715885, ECO:0000269|PubMed:22973015, ECO:0000269|PubMed:23994010, ECO:0000269|PubMed:25445488, ECO:0000269|PubMed:25730860, ECO:0000269|PubMed:25973519, ECO:0000269|PubMed:7920629, ECO:0000269|PubMed:7925268, ECO:0000269|PubMed:9009272, ECO:0000305|PubMed:8298642}.

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 DNAH12-GLRA1


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 DNAH12-GLRA1


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 DNAH12-GLRA1


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 DNAH12-GLRA1


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