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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:SAMD8-KAT6B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SAMD8-KAT6B
FusionPDB ID: 79103
FusionGDB2.0 ID: 79103
HgeneTgene
Gene symbol

SAMD8

KAT6B

Gene ID

142891

23522

Gene namesterile alpha motif domain containing 8lysine acetyltransferase 6B
SynonymsHEL-177|SMSrGTPTS|MORF|MOZ2|MYST4|ZC2HC6B|qkf|querkopf
Cytomap

10q22.2

10q22.2

Type of geneprotein-codingprotein-coding
Descriptionsphingomyelin synthase-related protein 1CPE synthaseHEL-S-181mPSAM domain-containing protein 8ceramide phosphoethanolamine synthaseepididymis luminal protein 177epididymis secretory sperm binding protein Li 181mPsphingomyelin synthase relatedsterihistone acetyltransferase KAT6BK(lysine) acetyltransferase 6BMOZ, YBF2/SAS3, SAS2 and TIP60 protein 4MOZ-related factorMYST histone acetyltransferase (monocytic leukemia) 4MYST-4histone acetyltransferase MORFhistone acetyltransferase MOZ2histone a
Modification date2020031320200313
UniProtAcc.

Q8WYB5

Ensembl transtripts involved in fusion geneENST idsENST00000372687, ENST00000372690, 
ENST00000542569, 
ENST00000490365, 
ENST00000287239, ENST00000372711, 
ENST00000372724, ENST00000372725, 
ENST00000372714, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 5=1807 X 11 X 4=308
# samples 810
** MAII scorelog2(8/180*10)=-1.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/308*10)=-1.62293035092018
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SAMD8 [Title/Abstract] AND KAT6B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SAMD8(76928416)-KAT6B(76788247), # samples:1
Anticipated loss of major functional domain due to fusion event.SAMD8-KAT6B seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
SAMD8-KAT6B seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
HgeneSAMD8

GO:0046513

ceramide biosynthetic process

19506037

HgeneSAMD8

GO:2000303

regulation of ceramide biosynthetic process

19506037

TgeneKAT6B

GO:0016573

histone acetylation

11965546

TgeneKAT6B

GO:0043966

histone H3 acetylation

16387653

TgeneKAT6B

GO:0045892

negative regulation of transcription, DNA-templated

10497217

TgeneKAT6B

GO:0045893

positive regulation of transcription, DNA-templated

10497217|11965546


check buttonFusion gene breakpoints across SAMD8 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across KAT6B (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4LUADTCGA-44-7660-01ASAMD8chr10

76928416

-KAT6Bchr10

76788247

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000542569SAMD8chr1076928416-ENST00000372714KAT6Bchr1076788247+35978958313452873
ENST00000372687SAMD8chr1076928416-ENST00000372714KAT6Bchr1076788247+35798778133434873
ENST00000372690SAMD8chr1076928416-ENST00000372714KAT6Bchr1076788247+376110599953616873

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000542569ENST00000372714SAMD8chr1076928416-KAT6Bchr1076788247+0.0060668160.99393314
ENST00000372687ENST00000372714SAMD8chr1076928416-KAT6Bchr1076788247+0.0064156620.99358433
ENST00000372690ENST00000372714SAMD8chr1076928416-KAT6Bchr1076788247+0.0061751280.99382484

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>79103_79103_1_SAMD8-KAT6B_SAMD8_chr10_76928416_ENST00000372687_KAT6B_chr10_76788247_ENST00000372714_length(amino acids)=873AA_BP=21
MLYHVCDLPLRARTTPAVYWKDNMNDDSSNLKEGSKDNPEPLKCKQVWPKGTKRGLSKWRQNKERKTGFKLNLYTPPETPMEPDEQVTVE
EQKETSEGKTSPSPIRIEEEVKETGEALLPQEENRREETCAPVSPNTSPGEKPEDDLIKPEEEEEEEEEEEEEEEEEEGEEEEGGGNVEK
DPDGAKSQEKEEPEISTEKEDSARLDDHEEEEEEDEEPSHNEDHDADDEDDSHMESAEVEKEELPRESFKEVLENQETFLDLNVQPGHSN
PEVLMDCGVDLTASCNSEPKELAGDPEAVPESDEEPPPGEQAQKQDQKNSKEVDTEFKEGNPATMEIDSETVQAVQSLTQESSEQDDTFQ
DCAETQEACRSLQNYTRADQSPQIATTLDDCQQSDHSSPVSSVHSHPGQSVRSVNSPSVPALENSYAQISPDQSAISVPSLQNMETSPMM
DVPSVSDHSQQVVDSGFSDLGSIESTTENYENPSSYDSTMGGSICGNGSSQNSCSYSNLTSSSLTQSSCAVTQQMSNISGSCSMLQQTSI
SSPPTCSVKSPQGCVVERPPSSSQQLAQCSMAANFTPPMQLAEIPETSNANIGLYERMGQSDFGAGHYPQPSATFSLAKLQQLTNTLIDH
SLPYSHSAAVTSYANSASLSTPLSNTGLVQLSQSPHSVPGGPQAQATMTPPPNLTPPPMNLPPPLLQRNMAASNIGISHSQRLQTQIASK
GHISMRTKSASLSPAAATHQSQIYGRSQTVAMQGPARTLTMQRGMNMSVNLMPAPAYNVNSVNMNMNTLNAMNGYSMSQPMMNSGYHSNH

--------------------------------------------------------------

>79103_79103_2_SAMD8-KAT6B_SAMD8_chr10_76928416_ENST00000372690_KAT6B_chr10_76788247_ENST00000372714_length(amino acids)=873AA_BP=21
MLYHVCDLPLRARTTPAVYWKDNMNDDSSNLKEGSKDNPEPLKCKQVWPKGTKRGLSKWRQNKERKTGFKLNLYTPPETPMEPDEQVTVE
EQKETSEGKTSPSPIRIEEEVKETGEALLPQEENRREETCAPVSPNTSPGEKPEDDLIKPEEEEEEEEEEEEEEEEEEGEEEEGGGNVEK
DPDGAKSQEKEEPEISTEKEDSARLDDHEEEEEEDEEPSHNEDHDADDEDDSHMESAEVEKEELPRESFKEVLENQETFLDLNVQPGHSN
PEVLMDCGVDLTASCNSEPKELAGDPEAVPESDEEPPPGEQAQKQDQKNSKEVDTEFKEGNPATMEIDSETVQAVQSLTQESSEQDDTFQ
DCAETQEACRSLQNYTRADQSPQIATTLDDCQQSDHSSPVSSVHSHPGQSVRSVNSPSVPALENSYAQISPDQSAISVPSLQNMETSPMM
DVPSVSDHSQQVVDSGFSDLGSIESTTENYENPSSYDSTMGGSICGNGSSQNSCSYSNLTSSSLTQSSCAVTQQMSNISGSCSMLQQTSI
SSPPTCSVKSPQGCVVERPPSSSQQLAQCSMAANFTPPMQLAEIPETSNANIGLYERMGQSDFGAGHYPQPSATFSLAKLQQLTNTLIDH
SLPYSHSAAVTSYANSASLSTPLSNTGLVQLSQSPHSVPGGPQAQATMTPPPNLTPPPMNLPPPLLQRNMAASNIGISHSQRLQTQIASK
GHISMRTKSASLSPAAATHQSQIYGRSQTVAMQGPARTLTMQRGMNMSVNLMPAPAYNVNSVNMNMNTLNAMNGYSMSQPMMNSGYHSNH

--------------------------------------------------------------

>79103_79103_3_SAMD8-KAT6B_SAMD8_chr10_76928416_ENST00000542569_KAT6B_chr10_76788247_ENST00000372714_length(amino acids)=873AA_BP=21
MLYHVCDLPLRARTTPAVYWKDNMNDDSSNLKEGSKDNPEPLKCKQVWPKGTKRGLSKWRQNKERKTGFKLNLYTPPETPMEPDEQVTVE
EQKETSEGKTSPSPIRIEEEVKETGEALLPQEENRREETCAPVSPNTSPGEKPEDDLIKPEEEEEEEEEEEEEEEEEEGEEEEGGGNVEK
DPDGAKSQEKEEPEISTEKEDSARLDDHEEEEEEDEEPSHNEDHDADDEDDSHMESAEVEKEELPRESFKEVLENQETFLDLNVQPGHSN
PEVLMDCGVDLTASCNSEPKELAGDPEAVPESDEEPPPGEQAQKQDQKNSKEVDTEFKEGNPATMEIDSETVQAVQSLTQESSEQDDTFQ
DCAETQEACRSLQNYTRADQSPQIATTLDDCQQSDHSSPVSSVHSHPGQSVRSVNSPSVPALENSYAQISPDQSAISVPSLQNMETSPMM
DVPSVSDHSQQVVDSGFSDLGSIESTTENYENPSSYDSTMGGSICGNGSSQNSCSYSNLTSSSLTQSSCAVTQQMSNISGSCSMLQQTSI
SSPPTCSVKSPQGCVVERPPSSSQQLAQCSMAANFTPPMQLAEIPETSNANIGLYERMGQSDFGAGHYPQPSATFSLAKLQQLTNTLIDH
SLPYSHSAAVTSYANSASLSTPLSNTGLVQLSQSPHSVPGGPQAQATMTPPPNLTPPPMNLPPPLLQRNMAASNIGISHSQRLQTQIASK
GHISMRTKSASLSPAAATHQSQIYGRSQTVAMQGPARTLTMQRGMNMSVNLMPAPAYNVNSVNMNMNTLNAMNGYSMSQPMMNSGYHSNH

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr10:76928416/chr10:76788247)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.KAT6B

Q8WYB5

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Histone acetyltransferase which may be involved in both positive and negative regulation of transcription. Required for RUNX2-dependent transcriptional activation. May be involved in cerebral cortex development. Component of the MOZ/MORF complex which has a histone H3 acetyltransferase activity. {ECO:0000269|PubMed:10497217, ECO:0000269|PubMed:11965546, ECO:0000269|PubMed:16387653}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-4512_78264.0327.0DomainSAM
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-4612_78327.0479.0DomainSAM
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-4612_78264.0416.0DomainSAM
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45153_173264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45201_221264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45232_252264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46153_173327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46201_221327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46232_252327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46277_297327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46153_173264.0416.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46201_221264.0416.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46232_252264.0416.0TransmembraneHelical
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181351_13731221.33333333333332074.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181409_14171221.33333333333332074.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181594_17631221.33333333333332074.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181961_20611221.33333333333332074.0Compositional biasNote=Met-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171070_11041038.33333333333331891.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171204_12071038.33333333333331891.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171351_13731038.33333333333331891.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171409_14171038.33333333333331891.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171594_17631038.33333333333331891.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271115171961_20611038.33333333333331891.0Compositional biasNote=Met-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171070_1104929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171204_1207929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171351_1373929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171409_1417929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171594_1763929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037271415171961_2061929.33333333333341782.0Compositional biasNote=Met-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181070_1104929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181204_1207929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181351_1373929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181409_1417929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181594_1763929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272416181961_2061929.33333333333341782.0Compositional biasNote=Met-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171070_1104929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171204_1207929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171351_1373929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171409_1417929.33333333333341782.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171594_1763929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000037272515171961_2061929.33333333333341782.0Compositional biasNote=Met-rich

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45368_415264.0327.0Topological domainCytoplasmic
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46368_415327.0479.0Topological domainCytoplasmic
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46368_415264.0416.0Topological domainCytoplasmic
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45277_297264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45322_342264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372687-45347_367264.0327.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46322_342327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000372690-46347_367327.0479.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46277_297264.0416.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46322_342264.0416.0TransmembraneHelical
HgeneSAMD8chr10:76928416chr10:76788247ENST00000542569-46347_367264.0416.0TransmembraneHelical
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181070_11041221.33333333333332074.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST0000028723916181204_12071221.33333333333332074.0Compositional biasNote=Poly-Glu
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618492_5331221.33333333333332074.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618521_5241221.33333333333332074.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618599_6051221.33333333333332074.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517492_5331038.33333333333331891.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517521_5241038.33333333333331891.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517599_6051038.33333333333331891.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517492_533929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517521_524929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517599_605929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618492_533929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618521_524929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618599_605929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517492_533929.33333333333341782.0Compositional biasNote=Ser-rich
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517521_524929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517599_605929.33333333333341782.0Compositional biasNote=Poly-Ser
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618103_1761221.33333333333332074.0DomainH15
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618715_9891221.33333333333332074.0DomainMYST-type HAT
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517103_1761038.33333333333331891.0DomainH15
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517715_9891038.33333333333331891.0DomainMYST-type HAT
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517103_176929.33333333333341782.0DomainH15
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517715_989929.33333333333341782.0DomainMYST-type HAT
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618103_176929.33333333333341782.0DomainH15
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618715_989929.33333333333341782.0DomainMYST-type HAT
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517103_176929.33333333333341782.0DomainH15
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517715_989929.33333333333341782.0DomainMYST-type HAT
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618361_7171221.33333333333332074.0RegionNote=Negatively regulates HAT activity
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618718_10081221.33333333333332074.0RegionNote=Catalytic
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618856_8601221.33333333333332074.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618865_8711221.33333333333332074.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517361_7171038.33333333333331891.0RegionNote=Negatively regulates HAT activity
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517718_10081038.33333333333331891.0RegionNote=Catalytic
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517856_8601038.33333333333331891.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517865_8711038.33333333333331891.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517361_717929.33333333333341782.0RegionNote=Negatively regulates HAT activity
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517718_1008929.33333333333341782.0RegionNote=Catalytic
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517856_860929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517865_871929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618361_717929.33333333333341782.0RegionNote=Negatively regulates HAT activity
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618718_1008929.33333333333341782.0RegionNote=Catalytic
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618856_860929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618865_871929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517361_717929.33333333333341782.0RegionNote=Negatively regulates HAT activity
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517718_1008929.33333333333341782.0RegionNote=Catalytic
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517856_860929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517865_871929.33333333333341782.0RegionAcetyl-CoA binding
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618213_2721221.33333333333332074.0Zinc fingerPHD-type 1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618269_3201221.33333333333332074.0Zinc fingerPHD-type 2
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618748_7731221.33333333333332074.0Zinc fingerC2HC MYST-type
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517213_2721038.33333333333331891.0Zinc fingerPHD-type 1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517269_3201038.33333333333331891.0Zinc fingerPHD-type 2
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517748_7731038.33333333333331891.0Zinc fingerC2HC MYST-type
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517213_272929.33333333333341782.0Zinc fingerPHD-type 1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517269_320929.33333333333341782.0Zinc fingerPHD-type 2
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517748_773929.33333333333341782.0Zinc fingerC2HC MYST-type
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618213_272929.33333333333341782.0Zinc fingerPHD-type 1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618269_320929.33333333333341782.0Zinc fingerPHD-type 2
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618748_773929.33333333333341782.0Zinc fingerC2HC MYST-type
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517213_272929.33333333333341782.0Zinc fingerPHD-type 1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517269_320929.33333333333341782.0Zinc fingerPHD-type 2
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517748_773929.33333333333341782.0Zinc fingerC2HC MYST-type


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
SAMD8
KAT6B


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
TgeneKAT6Bchr10:76928416chr10:76788247ENST000002872391618752_10081221.33333333333332074.0BRPF1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727111517752_10081038.33333333333331891.0BRPF1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727141517752_1008929.33333333333341782.0BRPF1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727241618752_1008929.33333333333341782.0BRPF1
TgeneKAT6Bchr10:76928416chr10:76788247ENST000003727251517752_1008929.33333333333341782.0BRPF1


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Related Drugs to SAMD8-KAT6B


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to SAMD8-KAT6B


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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