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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:ALDH3A2-SMC1A (FusionGDB2 ID:3904)

Fusion Gene Summary for ALDH3A2-SMC1A

check button Fusion gene summary
Fusion gene informationFusion gene name: ALDH3A2-SMC1A
Fusion gene ID: 3904
HgeneTgene
Gene symbol

ALDH3A2

SMC1A

Gene ID

224

8243

Gene namealdehyde dehydrogenase 3 family member A2structural maintenance of chromosomes 1A
SynonymsALDH10|FALDH|SLSCDLS2|DXS423E|SB1.8|SMC1|SMC1L1|SMC1alpha|SMCB
Cytomap

17p11.2

Xp11.22

Type of geneprotein-codingprotein-coding
Descriptionaldehyde dehydrogenase family 3 member A2aldehyde dehydrogenase 10fatty aldehyde dehydrogenasemicrosomal aldehyde dehydrogenasestructural maintenance of chromosomes protein 1ASMC protein 1ASMC-1-alphaSMC1 (structural maintenance of chromosomes 1, yeast)-like 1epididymis secretory sperm binding proteinsegregation of mitotic chromosomes 1
Modification date2020031520200329
UniProtAcc

P51648

.
Ensembl transtripts involved in fusion geneENST00000176643, ENST00000339618, 
ENST00000395575, ENST00000571163, 
ENST00000574597, ENST00000579855, 
ENST00000581518, 
ENST00000322213, 
ENST00000375340, ENST00000469129, 
Fusion gene scores* DoF score6 X 5 X 5=1507 X 6 X 4=168
# samples 67
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ALDH3A2 [Title/Abstract] AND SMC1A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointALDH3A2(19559029)-SMC1A(53438739), # 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
HgeneALDH3A2

GO:0006081

cellular aldehyde metabolic process

9133646

HgeneALDH3A2

GO:0046458

hexadecanal metabolic process

25047030

HgeneALDH3A2

GO:0055114

oxidation-reduction process

9133646

TgeneSMC1A

GO:0072423

response to DNA damage checkpoint signaling

11877377


check buttonFusion gene breakpoints across ALDH3A2 (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 SMC1A (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/ABF845221ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+


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Fusion Gene ORF analysis for ALDH3A2-SMC1A

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-3CDSENST00000176643ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000339618ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000395575ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000571163ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000574597ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000579855ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-3CDSENST00000581518ENST00000322213ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000176643ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000176643ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000339618ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000339618ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000395575ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000395575ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000571163ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000571163ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000574597ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000574597ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000579855ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000579855ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000581518ENST00000375340ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+
intron-intronENST00000581518ENST00000469129ALDH3A2chr17

19559029

+SMC1AchrX

53438739

+

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 ALDH3A2-SMC1A


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 ALDH3A2-SMC1A


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/:19559029/:53438739)
- 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
ALDH3A2

P51648

.
FUNCTION: Catalyzes the oxidation of medium and long chain aliphatic aldehydes to fatty acids. Active on a variety of saturated and unsaturated aliphatic aldehydes between 6 and 24 carbons in length (PubMed:9133646, PubMed:22633490, PubMed:25047030, PubMed:18035827, PubMed:9662422, PubMed:18182499). Responsible for conversion of the sphingosine 1-phosphate (S1P) degradation product hexadecenal to hexadecenoic acid (PubMed:22633490). {ECO:0000269|PubMed:18035827, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:22633490, ECO:0000269|PubMed:25047030, ECO:0000269|PubMed:9133646, ECO:0000269|PubMed:9662422}.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 ALDH3A2-SMC1A


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 ALDH3A2-SMC1A


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 ALDH3A2-SMC1A


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 ALDH3A2-SMC1A


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