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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: 32814

FusionGeneSummary for SCD_SLC25A26

check button Fusion gene summary
Fusion gene informationFusion gene name: SCD_SLC25A26
Fusion gene ID: 32814
HgeneTgene
Gene symbol

SCD

SLC25A26

Gene ID

6319

115286

Gene namestearoyl-CoA desaturasesolute carrier family 25 member 26
SynonymsFADS5|MSTP008|SCD1|SCDOS|hSCD1COXPD28|SAMC
Cytomap

10q24.31

3p14.1

Type of geneprotein-codingprotein-coding
Descriptionacyl-CoA desaturasedelta(9)-desaturasefatty acid desaturasepredicted protein of HQ0998stearoyl-CoA desaturase (delta-9-desaturase)stearoyl-CoA desaturase opposite strandS-adenosylmethionine mitochondrial carrier proteinmitochondrial S-adenosylmethionine transportersolute carrier family 25 (S-adenosylmethionine carrier), member 26solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 26
Modification date2018052320180523
UniProtAcc

O00767

Q70HW3

Ensembl transtripts involved in fusion geneENST00000370355, ENST00000354883, 
ENST00000336733, ENST00000536651, 
ENST00000413054, ENST00000484768, 
Fusion gene scores* DoF score4 X 4 X 3=484 X 5 X 5=100
# samples 45
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SCD [Title/Abstract] AND SLC25A26 [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
HgeneSCD

GO:0006636

unsaturated fatty acid biosynthetic process

15907797|18765284


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
ChiTaRS3.1BP243784SCDchr10

102108082

+SLC25A26chr3

66430857

-
* 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
5CDS-intronENST00000370355ENST00000354883SCDchr10

102108082

+SLC25A26chr3

66430857

-
5CDS-intronENST00000370355ENST00000336733SCDchr10

102108082

+SLC25A26chr3

66430857

-
5CDS-3UTRENST00000370355ENST00000536651SCDchr10

102108082

+SLC25A26chr3

66430857

-
5CDS-intronENST00000370355ENST00000413054SCDchr10

102108082

+SLC25A26chr3

66430857

-
5CDS-intronENST00000370355ENST00000484768SCDchr10

102108082

+SLC25A26chr3

66430857

-

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FusionProtFeatures for SCD_SLC25A26


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

O00767

SLC25A26

Q70HW3

Mitochondrial solute carriers shuttle metabolites,nucleotides, and cofactors through the mitochondrial innermembrane. Specifically mediates the transport of S-adenosylmethionine (SAM) into the mitochondria.{ECO:0000269|PubMed:14674884, ECO:0000269|PubMed:26522469}.

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 SCD_SLC25A26


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 SCD_SLC25A26


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 SCD_SLC25A26


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for SCD_SLC25A26


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSCDC0024667Animal Mammary Neoplasms2CTD_human
HgeneSCDC0024668Mammary Neoplasms, Experimental2CTD_human
HgeneSCDC0023794Lipoidosis1CTD_human
HgeneSCDC0023903Liver neoplasms1CTD_human
HgeneSCDC0339143Thyroid associated opthalmopathies1CTD_human
HgeneSCDC2239176Liver carcinoma1CTD_human
TgeneSLC25A26C4225206COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 281ORPHANET;UNIPROT