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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: 7915

FusionGeneSummary for COL26A1_SNX12

check button Fusion gene summary
Fusion gene informationFusion gene name: COL26A1_SNX12
Fusion gene ID: 7915
HgeneTgene
Gene symbol

COL26A1

SNX12

Gene ID

136227

29934

Gene namecollagen type XXVI alpha 1 chainsorting nexin 12
SynonymsEMI6|EMID2|EMU2|SH2B-
Cytomap

7q22.1

Xq13.1

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-1(XXVI) chainEMI domain containing 2collagen, type XXVI, alpha 1emilin and multimerin domain-containing protein 2sorting nexin-12
Modification date2018052320180519
UniProtAcc

Q96A83

Q9UMY4

Ensembl transtripts involved in fusion geneENST00000397927, ENST00000313669, 
ENST00000528707, 
ENST00000374274, 
ENST00000465030, ENST00000276105, 
Fusion gene scores* DoF score4 X 4 X 3=481 X 1 X 1=1
# samples 41
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: COL26A1 [Title/Abstract] AND SNX12 [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
TgeneSNX12

GO:0010955

negative regulation of protein processing

22709416

TgeneSNX12

GO:0042177

negative regulation of protein catabolic process

22719997

TgeneSNX12

GO:0051224

negative regulation of protein transport

22719997

TgeneSNX12

GO:2000642

negative regulation of early endosome to late endosome transport

22719997


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
ChiTaRS3.1BF994737COL26A1chr7

101107055

-SNX12chrX

70222024

+
* 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
intron-intronENST00000397927ENST00000374274COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000397927ENST00000465030COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000397927ENST00000276105COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000313669ENST00000374274COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000313669ENST00000465030COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000313669ENST00000276105COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000528707ENST00000374274COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000528707ENST00000465030COL26A1chr7

101107055

-SNX12chrX

70222024

+
intron-intronENST00000528707ENST00000276105COL26A1chr7

101107055

-SNX12chrX

70222024

+

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FusionProtFeatures for COL26A1_SNX12


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COL26A1

Q96A83

SNX12

Q9UMY4

May be involved in several stages of intracellulartrafficking. {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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FusionGeneSequence for COL26A1_SNX12


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 COL26A1_SNX12


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 COL26A1_SNX12


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 COL26A1_SNX12


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