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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: 38195

FusionGeneSummary for TLN1_KCTD12

check button Fusion gene summary
Fusion gene informationFusion gene name: TLN1_KCTD12
Fusion gene ID: 38195
HgeneTgene
Gene symbol

TLN1

KCTD12

Gene ID

7094

115207

Gene nametalin 1potassium channel tetramerization domain containing 12
SynonymsILWEQ|TLN|talin-1C13orf2|PFET1|PFETIN
Cytomap

9p13.3

13q22.3

Type of geneprotein-codingprotein-coding
Descriptiontalin-1BTB/POZ domain-containing protein KCTD12potassium channel tetramerisation domain containing 12predominantly fetal expressed T1 domaintesticular tissue protein Li 100
Modification date2018052220180519
UniProtAcc

Q9Y490

Q96CX2

Ensembl transtripts involved in fusion geneENST00000314888, ENST00000540444, 
ENST00000464379, 
ENST00000377474, 
ENST00000317765, 
Fusion gene scores* DoF score7 X 10 X 3=2102 X 2 X 1=4
# samples 102
** MAII scorelog2(10/210*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: TLN1 [Title/Abstract] AND KCTD12 [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
ChiTaRS3.1AI343584TLN1chr9

35697494

+KCTD12chr13

77456517

+
* 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-3UTRENST00000314888ENST00000377474TLN1chr9

35697494

+KCTD12chr13

77456517

+
intron-3UTRENST00000314888ENST00000317765TLN1chr9

35697494

+KCTD12chr13

77456517

+
intron-3UTRENST00000540444ENST00000377474TLN1chr9

35697494

+KCTD12chr13

77456517

+
intron-3UTRENST00000540444ENST00000317765TLN1chr9

35697494

+KCTD12chr13

77456517

+
intron-3UTRENST00000464379ENST00000377474TLN1chr9

35697494

+KCTD12chr13

77456517

+
intron-3UTRENST00000464379ENST00000317765TLN1chr9

35697494

+KCTD12chr13

77456517

+

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FusionProtFeatures for TLN1_KCTD12


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TLN1

Q9Y490

KCTD12

Q96CX2

Probably involved in connections of major cytoskeletalstructures to the plasma membrane. High molecular weightcytoskeletal protein concentrated at regions of cell-substratumcontact and, in lymphocytes, at cell-cell contacts (Bysimilarity). {ECO:0000250}. Auxiliary subunit of GABA-B receptors that determine thepharmacology and kinetics of the receptor response. Increasesagonist potency and markedly alter the G-protein signaling of thereceptors by accelerating onset and promoting desensitization (Bysimilarity). {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 TLN1_KCTD12


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 TLN1_KCTD12


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 TLN1_KCTD12


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 TLN1_KCTD12


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTLN1C0027626Neoplasm Invasiveness1CTD_human
HgeneTLN1C0029456Osteoporosis1CTD_human
TgeneKCTD12C0005586Bipolar Disorder1PSYGENET
TgeneKCTD12C0036341Schizophrenia1PSYGENET
TgeneKCTD12C0525045Mood Disorders1PSYGENET