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: 42492

FusionGeneSummary for ZBTB24_STK32C

check button Fusion gene summary
Fusion gene informationFusion gene name: ZBTB24_STK32C
Fusion gene ID: 42492
HgeneTgene
Gene symbol

ZBTB24

STK32C

Gene ID

9841

282974

Gene namezinc finger and BTB domain containing 24serine/threonine kinase 32C
SynonymsBIF1|ICF2|PATZ2|ZNF450PKE|YANK3
Cytomap

6q21

10q26.3

Type of geneprotein-codingprotein-coding
Descriptionzinc finger and BTB domain-containing protein 24POZ (BTB) and AT hook containing zinc finger 2zinc finger protein 450serine/threonine-protein kinase 32CPKE protein kinasetesticular tissue protein Li 187yet another novel kinase 3
Modification date2018052320180523
UniProtAcc

O43167

Q86UX6

Ensembl transtripts involved in fusion geneENST00000230122, ENST00000368622, 
ENST00000368625, 
Fusion gene scores* DoF score3 X 3 X 2=183 X 2 X 2=12
# samples 33
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ZBTB24 [Title/Abstract] AND STK32C [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
TCGARVSARCTCGA-QQ-A5VA-01AZBTB24chr6

109797378

-STK32Cchr10

134059459

-
* 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-5UTRENST00000230122ENST00000368622ZBTB24chr6

109797378

-STK32Cchr10

134059459

-
5CDS-5UTRENST00000230122ENST00000368625ZBTB24chr6

109797378

-STK32Cchr10

134059459

-

Top

FusionProtFeatures for ZBTB24_STK32C


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZBTB24

O43167

STK32C

Q86UX6

May be involved in BMP2-induced transcription.{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 ZBTB24_STK32C


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 ZBTB24_STK32C


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
ZBTB24MDFI, STK24, CALM1, KDM1A, PRMT7, SUV39H1, PASK, BAX, DNM1L, AES, CDA, PHC2, KPNA3, KRTAP5-9, BLZF1, MID2, ZBTB43, POGZ, CCNDBP1, LDOC1, KLF15, BCL11A, HMBOX1, CEP76, CEP70, TSGA10, TSC22D4, KRTAP4-2, TRIM41, SSX2IP, KRT40, KRTAP10-7, KRTAP10-9, KRTAP10-1, KRTAP10-5, KRTAP10-8, KRTAP10-3, ZBTB8A, NOL12, RPL14, PRR11, RIN3, HIST1H2BG, PPAN, ZBTB48, ZNF169, E4F1, RPL7, H2AFX, ZNF512, ZNF71, RPS8, RPS14, RPL8, KIAA0020, ZNF324B, RBM4STK32CGRB2, C18orf8, HSP90AA1, HSP90AA5P, HSP90AA4P, FDFT1, CDC37, MCM5


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 ZBTB24_STK32C


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 ZBTB24_STK32C


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneZBTB24C3279748IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 21UNIPROT