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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: 12477

FusionGeneSummary for FAM111A_RNU6-246P

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM111A_RNU6-246P
Fusion gene ID: 12477
HgeneTgene
Gene symbol

FAM111A

RNU6-246P

Gene ID

63901

106481884

Gene namefamily with sequence similarity 111 member ARNA, U6 small nuclear 246, pseudogene
SynonymsGCLEB|KCS2-
Cytomap

11q12.1

9p22.3

Type of geneprotein-codingpseudo
Descriptionprotein FAM111A-
Modification date2018051920180329
UniProtAcc

Q96PZ2

Ensembl transtripts involved in fusion geneENST00000528737, ENST00000420244, 
ENST00000529985, ENST00000361723, 
ENST00000533703, ENST00000531147, 
ENST00000384702, 
Fusion gene scores* DoF score1 X 1 X 1=11 X 1 X 1=1
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: FAM111A [Title/Abstract] AND RNU6-246P [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
TCGALDBRCATCGA-A8-A06Q-01AFAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
* 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-3UTRENST00000528737ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
5CDS-3UTRENST00000420244ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
intron-3UTRENST00000529985ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
5CDS-3UTRENST00000361723ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
5CDS-3UTRENST00000533703ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+
5CDS-3UTRENST00000531147ENST00000384702FAM111Achr11

58920411

+RNU6-246Pchr9

15544242

+

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FusionProtFeatures for FAM111A_RNU6-246P


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM111A

Q96PZ2

RNU6-246P

Chromatin-associated protein required for PCNA loadingon replication sites. Promotes S-phase entry and DNA synthesis(PubMed:24561620). May directly function at replication forks,explaining why Simian virus 40 (SV40) interacts with FAM111A toovercome host range restriction (PubMed:23093934).{ECO:0000269|PubMed:23093934, ECO:0000269|PubMed:24561620}. 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}.

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 FAM111A_RNU6-246P


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 FAM111A_RNU6-246P


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
FAM111ACDC23, NOP56, NCSTN, TP53RNU6-246P


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 FAM111A_RNU6-246P


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 FAM111A_RNU6-246P


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFAM111AC0265291Kenny-Caffey syndrome3ORPHANET;UNIPROT
HgeneFAM111AC1865639Gracile bone dysplasia1ORPHANET;UNIPROT