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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: 12469

FusionGeneSummary for FAM107B_GCNT7

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM107B_GCNT7
Fusion gene ID: 12469
HgeneTgene
Gene symbol

FAM107B

GCNT7

Gene ID

83641

140687

Gene namefamily with sequence similarity 107 member Bglucosaminyl (N-acetyl) transferase family member 7
SynonymsC10orf45|HITSC20orf105|dJ1153D9.2|gcnt
Cytomap

10p13

20q13.31

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM107BFAM107B/CDNF fusionheat shock-inducible tumor small proteinbeta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 7beta 1,6-N-acetylglucosaminyltransferase
Modification date2018051920180329
UniProtAcc

Q9H098

Q6ZNI0

Ensembl transtripts involved in fusion geneENST00000181796, ENST00000378470, 
ENST00000468747, ENST00000378467, 
ENST00000378465, ENST00000378458, 
ENST00000478076, ENST00000378462, 
ENST00000496330, ENST00000479731, 
ENST00000471815, 
ENST00000243913, 
Fusion gene scores* DoF score5 X 5 X 2=502 X 2 X 2=8
# samples 52
** MAII scorelog2(5/50*10)=0log2(2/8*10)=1.32192809488736
Context

PubMed: FAM107B [Title/Abstract] AND GCNT7 [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
ChiTaRS3.1BQ375049FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
* 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-intronENST00000181796ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000378470ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000468747ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000378467ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000378465ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000378458ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000478076ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000378462ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000496330ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000479731ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+
intron-intronENST00000471815ENST00000243913FAM107Bchr10

14641776

+GCNT7chr20

55099683

+

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FusionProtFeatures for FAM107B_GCNT7


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM107B

Q9H098

GCNT7

Q6ZNI0

Glycosyltransferase. {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 FAM107B_GCNT7


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 FAM107B_GCNT7


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 FAM107B_GCNT7


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 FAM107B_GCNT7


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