FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 12641

FusionGeneSummary for FAM168B_FAM168B

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM168B_FAM168B
Fusion gene ID: 12641
HgeneTgene
Gene symbol

FAM168B

FAM168B

Gene ID

130074

130074

Gene namefamily with sequence similarity 168 member Bfamily with sequence similarity 168 member B
SynonymsMANIMANI
Cytomap

2q21.1

2q21.1

Type of geneprotein-codingprotein-coding
Descriptionmyelin-associated neurite-outgrowth inhibitorprotein FAM168Bmyelin-associated neurite-outgrowth inhibitorprotein FAM168B
Modification date2018051920180519
UniProtAcc

A1KXE4

A1KXE4

Ensembl transtripts involved in fusion geneENST00000409185, ENST00000389915, 
ENST00000409185, ENST00000389915, 
Fusion gene scores* DoF score5 X 7 X 2=705 X 7 X 2=70
# samples 77
** MAII scorelog2(7/70*10)=0log2(7/70*10)=0
Context

PubMed: FAM168B [Title/Abstract] AND FAM168B [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
ChiTaRS3.1CA311681FAM168Bchr2

131805603

+FAM168Bchr2

131805824

-
ChiTaRS3.1BE177741FAM168Bchr2

131843495

-FAM168Bchr2

131844024

+
ChiTaRS3.1BE872492FAM168Bchr2

131806593

+FAM168Bchr2

131806568

-
* 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-3UTRENST00000409185ENST00000409185FAM168Bchr2

131805603

+FAM168Bchr2

131805824

-
intron-intronENST00000409185ENST00000389915FAM168Bchr2

131805603

+FAM168Bchr2

131805824

-
intron-3UTRENST00000389915ENST00000409185FAM168Bchr2

131805603

+FAM168Bchr2

131805824

-
intron-intronENST00000389915ENST00000389915FAM168Bchr2

131805603

+FAM168Bchr2

131805824

-
intron-intronENST00000409185ENST00000409185FAM168Bchr2

131843495

-FAM168Bchr2

131844024

+
intron-intronENST00000409185ENST00000389915FAM168Bchr2

131843495

-FAM168Bchr2

131844024

+
intron-intronENST00000389915ENST00000409185FAM168Bchr2

131843495

-FAM168Bchr2

131844024

+
intron-intronENST00000389915ENST00000389915FAM168Bchr2

131843495

-FAM168Bchr2

131844024

+
intron-3UTRENST00000409185ENST00000409185FAM168Bchr2

131806593

+FAM168Bchr2

131806568

-
intron-intronENST00000409185ENST00000389915FAM168Bchr2

131806593

+FAM168Bchr2

131806568

-
intron-3UTRENST00000389915ENST00000409185FAM168Bchr2

131806593

+FAM168Bchr2

131806568

-
intron-intronENST00000389915ENST00000389915FAM168Bchr2

131806593

+FAM168Bchr2

131806568

-

Top

FusionProtFeatures for FAM168B_FAM168B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM168B

A1KXE4

FAM168B

A1KXE4

Modulates neuronal axonal outgrowth by acting as anegative regulator of CDC42 and STAT3 and a positive regulator ofSTMN2. Positive regulator of CDC27 (By similarity). {ECO:0000250}. Modulates neuronal axonal outgrowth by acting as anegative regulator of CDC42 and STAT3 and a positive regulator ofSTMN2. Positive regulator of CDC27 (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


Top

FusionGeneSequence for FAM168B_FAM168B


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).

Top

FusionGenePPI for FAM168B_FAM168B


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


Top

RelatedDrugs for FAM168B_FAM168B


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

Top

RelatedDiseases for FAM168B_FAM168B


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