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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:FAM172A-INHBA (FusionGDB2 ID:28702)

Fusion Gene Summary for FAM172A-INHBA

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM172A-INHBA
Fusion gene ID: 28702
HgeneTgene
Gene symbol

FAM172A

INHBA

Gene ID

83989

3624

Gene namefamily with sequence similarity 172 member Ainhibin subunit beta A
SynonymsC5orf21|ToupeeEDF|FRP
Cytomap

5q15

7p14.1

Type of geneprotein-codingprotein-coding
Descriptioncotranscriptional regulator FAM172Aprotein FAM172Ainhibin beta A chainFSH-releasing proteinInhibin, beta-1activin beta-A chainerythroid differentiation factorerythroid differentiation proteinfollicle-stimulating hormone-releasing proteininhibin beta A subunitinhibin, beta A (activin A, activin AB
Modification date2020031320200315
UniProtAcc

Q8WUF8

.
Ensembl transtripts involved in fusion geneENST00000395965, ENST00000504768, 
ENST00000505869, ENST00000509163, 
ENST00000509739, 
ENST00000242208, 
ENST00000442711, ENST00000464515, 
Fusion gene scores* DoF score18 X 17 X 8=24483 X 3 X 1=9
# samples 233
** MAII scorelog2(23/2448*10)=-3.41189779174828
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FAM172A [Title/Abstract] AND INHBA [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFAM172A(93018209)-INHBA(41740092), # 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
TgeneINHBA

GO:0000082

G1/S transition of mitotic cell cycle

9884026

TgeneINHBA

GO:0002244

hematopoietic progenitor cell differentiation

15451575

TgeneINHBA

GO:0006357

regulation of transcription by RNA polymerase II

11948405

TgeneINHBA

GO:0007050

cell cycle arrest

9884026

TgeneINHBA

GO:0008285

negative regulation of cell proliferation

11948405

TgeneINHBA

GO:0010628

positive regulation of gene expression

23812417

TgeneINHBA

GO:0010862

positive regulation of pathway-restricted SMAD protein phosphorylation

19736306

TgeneINHBA

GO:0021773

striatal medium spiny neuron differentiation

25804741

TgeneINHBA

GO:0030308

negative regulation of cell growth

9884026|20573232

TgeneINHBA

GO:0032270

positive regulation of cellular protein metabolic process

21828274

TgeneINHBA

GO:0032924

activin receptor signaling pathway

9884026

TgeneINHBA

GO:0035987

endodermal cell differentiation

21828274

TgeneINHBA

GO:0042493

response to drug

20573232

TgeneINHBA

GO:0042541

hemoglobin biosynthetic process

1310063

TgeneINHBA

GO:0045648

positive regulation of erythrocyte differentiation

9032295

TgeneINHBA

GO:0045786

negative regulation of cell cycle

9884026

TgeneINHBA

GO:0045893

positive regulation of transcription, DNA-templated

21281489

TgeneINHBA

GO:0045944

positive regulation of transcription by RNA polymerase II

12702211|21281489

TgeneINHBA

GO:0097154

GABAergic neuron differentiation

25804741

TgeneINHBA

GO:0097191

extrinsic apoptotic signaling pathway

9884026

TgeneINHBA

GO:2001241

positive regulation of extrinsic apoptotic signaling pathway in absence of ligand

8267637


check buttonFusion gene breakpoints across FAM172A (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 INHBA (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/ABC016716FAM172Achr5

93018209

-INHBAchr7

41740092

-


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Fusion Gene ORF analysis for FAM172A-INHBA

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-5UTRENST00000395965ENST00000242208FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000395965ENST00000442711FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000504768ENST00000242208FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000504768ENST00000442711FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000505869ENST00000242208FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000505869ENST00000442711FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000509163ENST00000242208FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000509163ENST00000442711FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000509739ENST00000242208FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-5UTRENST00000509739ENST00000442711FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-intronENST00000395965ENST00000464515FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-intronENST00000504768ENST00000464515FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-intronENST00000505869ENST00000464515FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-intronENST00000509163ENST00000464515FAM172Achr5

93018209

-INHBAchr7

41740092

-
intron-intronENST00000509739ENST00000464515FAM172Achr5

93018209

-INHBAchr7

41740092

-

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 FAM172A-INHBA


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 FAM172A-INHBA


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/:93018209/:41740092)
- 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
FAM172A

Q8WUF8

.
FUNCTION: Plays a role in the regulation of alternative splicing, by interacting with AGO2 and CHD7. Seems to be required for stabilizing protein-protein interactions at the chromatin-spliceosome interface. May have hydrolase activity. {ECO:0000250|UniProtKB:Q3TNH5}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 FAM172A-INHBA


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 FAM172A-INHBA


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 FAM172A-INHBA


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 FAM172A-INHBA


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