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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:GH1-HDAC1 (FusionGDB2 ID:32945)

Fusion Gene Summary for GH1-HDAC1

check button Fusion gene summary
Fusion gene informationFusion gene name: GH1-HDAC1
Fusion gene ID: 32945
HgeneTgene
Gene symbol

GH1

HDAC1

Gene ID

2688

3065

Gene namegrowth hormone 1histone deacetylase 1
SynonymsGH|GH-N|GHB5|GHN|IGHD1A|IGHD1B|IGHD2|hGH-NGON-10|HD1|KDAC1|RPD3|RPD3L1
Cytomap

17q23.3

1p35.2-p35.1

Type of geneprotein-codingprotein-coding
Descriptionsomatotropingrowth hormone B5pituitary growth hormonehistone deacetylase 1reduced potassium dependency, yeast homolog-like 1
Modification date2020032220200327
UniProtAcc.

Q96DB2

Ensembl transtripts involved in fusion geneENST00000351388, ENST00000458650, 
ENST00000323322, ENST00000342364, 
ENST00000373548, ENST00000373541, 
ENST00000490081, 
Fusion gene scores* DoF score2 X 2 X 1=412 X 11 X 6=792
# samples 213
** MAII scorelog2(2/4*10)=2.32192809488736log2(13/792*10)=-2.60698880705116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GH1 [Title/Abstract] AND HDAC1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGH1(61995453)-HDAC1(32792598), # 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
HgeneGH1

GO:0002092

positive regulation of receptor internalization

9360546

HgeneGH1

GO:0010536

positive regulation of activation of Janus kinase activity

8063815|12552091

HgeneGH1

GO:0010828

positive regulation of glucose transmembrane transport

9144201

HgeneGH1

GO:0014068

positive regulation of phosphatidylinositol 3-kinase signaling

7782332

HgeneGH1

GO:0032355

response to estradiol

12552091

HgeneGH1

GO:0040018

positive regulation of multicellular organism growth

7565946|20110402

HgeneGH1

GO:0042531

positive regulation of tyrosine phosphorylation of STAT protein

8923468|12552091

HgeneGH1

GO:0043568

positive regulation of insulin-like growth factor receptor signaling pathway

7565946

HgeneGH1

GO:0046427

positive regulation of JAK-STAT cascade

8063815|8923468

HgeneGH1

GO:0050731

positive regulation of peptidyl-tyrosine phosphorylation

7782332

HgeneGH1

GO:0060396

growth hormone receptor signaling pathway

8063815

HgeneGH1

GO:0070977

bone maturation

20110402

TgeneHDAC1

GO:0000122

negative regulation of transcription by RNA polymerase II

18854353

TgeneHDAC1

GO:0006476

protein deacetylation

17172643|23629966

TgeneHDAC1

GO:0045893

positive regulation of transcription, DNA-templated

16762839

TgeneHDAC1

GO:0045944

positive regulation of transcription by RNA polymerase II

16762839

TgeneHDAC1

GO:0060766

negative regulation of androgen receptor signaling pathway

15919722

TgeneHDAC1

GO:0070932

histone H3 deacetylation

12590135

TgeneHDAC1

GO:0070933

histone H4 deacetylation

12590135


check buttonFusion gene breakpoints across GH1 (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 HDAC1 (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/AAV748376GH1chr17

61995453

-HDAC1chr1

32792598

+


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Fusion Gene ORF analysis for GH1-HDAC1

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-3CDSENST00000351388ENST00000373548GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-5UTRENST00000351388ENST00000373541GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-intronENST00000351388ENST00000490081GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-3CDSENST00000458650ENST00000373548GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-5UTRENST00000458650ENST00000373541GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-intronENST00000458650ENST00000490081GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-3CDSENST00000323322ENST00000373548GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-5UTRENST00000323322ENST00000373541GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-intronENST00000323322ENST00000490081GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-3CDSENST00000342364ENST00000373548GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-5UTRENST00000342364ENST00000373541GH1chr17

61995453

-HDAC1chr1

32792598

+
intron-intronENST00000342364ENST00000490081GH1chr17

61995453

-HDAC1chr1

32792598

+

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 GH1-HDAC1


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 GH1-HDAC1


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
.HDAC1

Q96DB2

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: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. {ECO:0000269|PubMed:11948178}.

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 GH1-HDAC1


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 GH1-HDAC1


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 GH1-HDAC1


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 GH1-HDAC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGH1C0001206Acromegaly7CTD_human
HgeneGH1C0001973Alcoholic Intoxication, Chronic5PSYGENET
HgeneGH1C0271567Isolated Growth Hormone Deficiency, Type II4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneGH1C1849779Kowarski syndrome4CTD_human;ORPHANET;UNIPROT
HgeneGH1C0011570Mental Depression3PSYGENET
HgeneGH1C0011581Depressive disorder3PSYGENET
HgeneGH1C2748571Isolated Growth Hormone Deficiency, Type IB3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneGH1C0024668Mammary Neoplasms, Experimental2CTD_human
HgeneGH1C0342573PITUITARY DWARFISM I2CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneGH1C0346302Growth Hormone-Secreting Pituitary Adenoma2CTD_human
HgeneGH1C3489630Somatotrophinoma, Familial2CTD_human
HgeneGH1C4748435ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V2ORPHANET
HgeneGH1C0007222Cardiovascular Diseases1CTD_human
HgeneGH1C0018273Growth Disorders1CTD_human
HgeneGH1C0021655Insulin Resistance1CTD_human
HgeneGH1C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneGH1C0026846Muscular Atrophy1CTD_human
HgeneGH1C0028754Obesity1CTD_human
HgeneGH1C0032000Pituitary Adenoma1CTD_human
HgeneGH1C0032019Pituitary Neoplasms1CTD_human
HgeneGH1C0032461Polycythemia1CTD_human
HgeneGH1C0041408Turner Syndrome1CTD_human
HgeneGH1C0043094Weight Gain1CTD_human
HgeneGH1C0242526Gonadal Dysgenesis, 45,X1CTD_human
HgeneGH1C0242528Azotemia1CTD_human
HgeneGH1C0270948Neurogenic Muscular Atrophy1CTD_human
HgeneGH1C0346300Pituitary carcinoma1CTD_human
HgeneGH1C0920563Insulin Sensitivity1CTD_human
HgeneGH1C1527168Bonnevie-Ullrich Syndrome1CTD_human
HgeneGH1C1527405Erythrocytosis1CTD_human
TgeneHDAC1C0036341Schizophrenia2PSYGENET
TgeneHDAC1C0007137Squamous cell carcinoma1CTD_human
TgeneHDAC1C0014175Endometriosis1CTD_human
TgeneHDAC1C0018799Heart Diseases1CTD_human
TgeneHDAC1C0269102Endometrioma1CTD_human
TgeneHDAC1C0340543Familial primary pulmonary hypertension1CTD_human
TgeneHDAC1C0525045Mood Disorders1PSYGENET
TgeneHDAC1C1969342PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED1CTD_human
TgeneHDAC1C1969343Pulmonary Hypertension, Primary, Fenfluramine-Associated1CTD_human
TgeneHDAC1C2713368Hematopoetic Myelodysplasia1CTD_human
TgeneHDAC1C3203102Idiopathic pulmonary arterial hypertension1CTD_human
TgeneHDAC1C3463824MYELODYSPLASTIC SYNDROME1CTD_human
TgeneHDAC1C3714844Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia1CTD_human
TgeneHDAC1C4552070Pulmonary Hypertension, Primary, 11CTD_human