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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 12528

FusionGeneSummary for FAM127A_ACADSB

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM127A_ACADSB
Fusion gene ID: 12528
HgeneTgene
Gene symbol

FAM127A

ACADSB

Gene ID

36

Gene nameacyl-CoA dehydrogenase short/branched chain
Synonyms2-MEBCAD|ACAD7|SBCAD
Cytomap

10q26.13

Type of geneprotein-coding
Descriptionshort/branched chain specific acyl-CoA dehydrogenase, mitochondrial2-methyl branched chain acyl-CoA dehydrogenase2-methylbutyryl-coenzyme A dehydrogenaseacyl-Coenzyme A dehydrogenase, short/branched chain
Modification date20180523
UniProtAcc

P45954

Ensembl transtripts involved in fusion geneENST00000257013, ENST00000464369, 
ENST00000368869, ENST00000358776, 
ENST00000496730, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 1=4
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: FAM127A [Title/Abstract] AND ACADSB [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1EB388356FAM127AchrX

134167195

+ACADSBchr10

124800157

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
3UTR-3CDSENST00000257013ENST00000368869FAM127AchrX

134167195

+ACADSBchr10

124800157

+
3UTR-3CDSENST00000257013ENST00000358776FAM127AchrX

134167195

+ACADSBchr10

124800157

+
3UTR-3UTRENST00000257013ENST00000496730FAM127AchrX

134167195

+ACADSBchr10

124800157

+
3UTR-3CDSENST00000464369ENST00000368869FAM127AchrX

134167195

+ACADSBchr10

124800157

+
3UTR-3CDSENST00000464369ENST00000358776FAM127AchrX

134167195

+ACADSBchr10

124800157

+
3UTR-3UTRENST00000464369ENST00000496730FAM127AchrX

134167195

+ACADSBchr10

124800157

+

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FusionProtFeatures for FAM127A_ACADSB


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM127A

ACADSB

P45954

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Has greatest activity toward short branched chain acyl-CoA derivative such as (s)-2-methylbutyryl-CoA, isobutyryl-CoA,and 2-methylhexanoyl-CoA as well as toward short straight chainacyl-CoAs such as butyryl-CoA and hexanoyl-CoA. Can use valproyl-CoA as substrate and may play a role in controlling the metabolicflux of valproic acid in the development of toxicity of thisagent.

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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FusionGeneSequence for FAM127A_ACADSB


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for FAM127A_ACADSB


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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RelatedDrugs for FAM127A_ACADSB


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneACADSBP45954DB00313Valproic AcidShort/branched chain specific acyl-CoA dehydrogenase, mitochondrialsmall moleculeapproved|investigational

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RelatedDiseases for FAM127A_ACADSB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneACADSBC0004352Autistic Disorder1CTD_human
TgeneACADSBC18649122-Methylbutyryl-CoA Dehydrogenase Deficiency1CTD_human;ORPHANET;UNIPROT