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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:KMT2C-SND1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KMT2C-SND1
FusionPDB ID: 43261
FusionGDB2.0 ID: 54215
HgeneTgene
Gene symbol

KMT2C

SND1

Gene ID

58508

27044

Gene namelysine methyltransferase 2Cstaphylococcal nuclease and tudor domain containing 1
SynonymsHALR|KLEFS2|MLL3TDRD11|Tudor-SN|p100
Cytomap

7q36.1

7q32.1

Type of geneprotein-codingprotein-coding
Descriptionhistone-lysine N-methyltransferase 2CALR-like proteinhistone-lysine N-methyltransferase MLL3histone-lysine N-methyltransferase, H3 lysine-4 specifichomologous to ALR proteinlysine (K)-specific methyltransferase 2Cmyeloid/lymphoid or mixed-lineage lestaphylococcal nuclease domain-containing protein 1EBNA2 coactivator p100testis tissue sperm-binding protein Li 82Ptudor domain-containing protein 11
Modification date2020032020200313
UniProtAcc

Q8NEZ4

Q7KZF4

Ensembl transtripts involved in fusion geneENST idsENST00000262189, ENST00000355193, 
ENST00000485241, ENST00000485655, 
ENST00000467238, ENST00000354725, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score26 X 23 X 12=717629 X 24 X 11=7656
# samples 3233
** MAII scorelog2(32/7176*10)=-4.4870360800319
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(33/7656*10)=-4.53605290024021
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KMT2C [Title/Abstract] AND SND1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KMT2C(152132711)-SND1(127447538), # samples:2
Anticipated loss of major functional domain due to fusion event.KMT2C-SND1 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.
KMT2C-SND1 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.
KMT2C-SND1 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.
KMT2C-SND1 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.
* 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
HgeneKMT2C

GO:0097692

histone H3-K4 monomethylation

26324722

TgeneSND1

GO:0010587

miRNA catabolic process

28546213


check buttonFusion gene breakpoints across KMT2C (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 SND1 (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
ChimerDB4ESCATCGA-L5-A8NI-01AKMT2Cchr7

152132711

-SND1chr7

127447538

+
ChimerDB4ESCATCGA-L5-A8NIKMT2Cchr7

152132711

-SND1chr7

127447538

+


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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)
ENST00000262189KMT2Cchr7152132711-ENST00000354725SND1chr7127447538+25103803951960521
ENST00000355193KMT2Cchr7152132711-ENST00000354725SND1chr7127447538+25103803951960521

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
ENST00000262189ENST00000354725KMT2Cchr7152132711-SND1chr7127447538+0.0042271320.9957729
ENST00000355193ENST00000354725KMT2Cchr7152132711-SND1chr7127447538+0.0042271320.9957729

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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

>43261_43261_1_KMT2C-SND1_KMT2C_chr7_152132711_ENST00000262189_SND1_chr7_127447538_ENST00000354725_length(amino acids)=521AA_BP=
MRPLYDIPYMFEAREFLRKKLIGKKVNVTVDYIRPASPATETVPAFSERTCATVTIGGINIAEALVSKGLATVIRYRQDDDQRSSHYDEL
LAAEARAIKNGKGLHSKKEVPIHRVADISGDTQKAKQFLPFLQRAGRSEAVVEYVFSGSRLKLYLPKETCLITFLLAGIECPRGARNLPG
LVQEGEPFSEEATLFTKELVLQREVEVEVESMDKAGNFIGWLHIDGANLSVLLVEHALSKVHFTAERSSYYKSLLSAEEAAKQKKEKVWA
HYEEQPVEEVMPVLEEKERSASYKPVFVTEITDDLHFYVQDVETGTQLEKLMENMRNDIASHPPVEGSYAPRRGEFCIAKFVDGEWYRAR
VEKVESPAKIHVFYIDYGNREVLPSTRLGTLSPAFSTRVLPAQATEYAFAFIQVPQDDDARTDAVDSVVRDIQNTQCLLNVEHLSAGCPH

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

>43261_43261_2_KMT2C-SND1_KMT2C_chr7_152132711_ENST00000355193_SND1_chr7_127447538_ENST00000354725_length(amino acids)=521AA_BP=
MRPLYDIPYMFEAREFLRKKLIGKKVNVTVDYIRPASPATETVPAFSERTCATVTIGGINIAEALVSKGLATVIRYRQDDDQRSSHYDEL
LAAEARAIKNGKGLHSKKEVPIHRVADISGDTQKAKQFLPFLQRAGRSEAVVEYVFSGSRLKLYLPKETCLITFLLAGIECPRGARNLPG
LVQEGEPFSEEATLFTKELVLQREVEVEVESMDKAGNFIGWLHIDGANLSVLLVEHALSKVHFTAERSSYYKSLLSAEEAAKQKKEKVWA
HYEEQPVEEVMPVLEEKERSASYKPVFVTEITDDLHFYVQDVETGTQLEKLMENMRNDIASHPPVEGSYAPRRGEFCIAKFVDGEWYRAR
VEKVESPAKIHVFYIDYGNREVLPSTRLGTLSPAFSTRVLPAQATEYAFAFIQVPQDDDARTDAVDSVVRDIQNTQCLLNVEHLSAGCPH

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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/chr7:152132711/chr7:127447538)
- 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
KMT2C

Q8NEZ4

SND1

Q7KZF4

FUNCTION: Histone methyltransferase that methylates 'Lys-4' of histone H3 (PubMed:22266653). H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. Central component of the MLL2/3 complex, a coactivator complex of nuclear receptors, involved in transcriptional coactivation. KMT2C/MLL3 may be a catalytic subunit of this complex. May be involved in leukemogenesis and developmental disorder. {ECO:0000269|PubMed:17500065, ECO:0000269|PubMed:22266653}.FUNCTION: Endonuclease that mediates miRNA decay of both protein-free and AGO2-loaded miRNAs (PubMed:28546213, PubMed:18453631). As part of its function in miRNA decay, regulates mRNAs involved in G1-to-S phase transition (PubMed:28546213). Functions as a bridging factor between STAT6 and the basal transcription factor (PubMed:12234934). Plays a role in PIM1 regulation of MYB activity (PubMed:9809063). Functions as a transcriptional coactivator for STAT5 (By similarity). {ECO:0000250|UniProtKB:Q78PY7, ECO:0000269|PubMed:12234934, ECO:0000269|PubMed:18453631, ECO:0000269|PubMed:28546213, ECO:0000269|PubMed:9809063}.; FUNCTION: (Microbial infection) Functions as a transcriptional coactivator for the Epstein-Barr virus nuclear antigen 2 (EBNA2). {ECO:0000269|PubMed:7651391}.

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
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-15934_4653.6666666666666644912.0DNA bindingNote=A.T hook
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-16034_4653.6666666666666644969.0DNA bindingNote=A.T hook
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924525_660384.0911.0DomainTNase-like 4
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924729_787384.0911.0DomainTudor
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924388_392384.0911.0MotifNuclear localization signal

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591338_136653.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591754_178753.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1593054_308153.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1593173_327253.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1593391_343353.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159644_67253.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-15992_11253.6666666666666644912.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601338_136653.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601754_178753.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1603054_308153.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1603173_327253.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1603391_343353.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160644_67253.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-16092_11253.6666666666666644969.0Coiled coilOntology_term=ECO:0000255
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591719_179653.6666666666666644912.0Compositional biasNote=Gln-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591834_228153.6666666666666644912.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1592412_263053.6666666666666644912.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1592690_278653.6666666666666644912.0Compositional biasNote=Asp-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1593012_350953.6666666666666644912.0Compositional biasNote=Gln-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1593277_338153.6666666666666644912.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601719_179653.6666666666666644969.0Compositional biasNote=Gln-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601834_228153.6666666666666644969.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1602412_263053.6666666666666644969.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1602690_278653.6666666666666644969.0Compositional biasNote=Asp-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1603012_350953.6666666666666644969.0Compositional biasNote=Gln-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1603277_338153.6666666666666644969.0Compositional biasNote=Pro-rich
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159436_48953.6666666666666644912.0DomainDHHC
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594545_460553.6666666666666644912.0DomainFYR N-terminal
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594606_469153.6666666666666644912.0DomainFYR C-terminal
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594771_488753.6666666666666644912.0DomainSET
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594895_491153.6666666666666644912.0DomainPost-SET
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160436_48953.6666666666666644969.0DomainDHHC
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604545_460553.6666666666666644969.0DomainFYR N-terminal
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604606_469153.6666666666666644969.0DomainFYR C-terminal
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604771_488753.6666666666666644969.0DomainSET
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604895_491153.6666666666666644969.0DomainPost-SET
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594848_484953.6666666666666644912.0RegionS-adenosyl-L-methionine binding
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604848_484953.6666666666666644969.0RegionS-adenosyl-L-methionine binding
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591007_105753.6666666666666644912.0Zinc fingerPHD-type 6
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1591084_113953.6666666666666644912.0Zinc fingerPHD-type 7
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159227_26253.6666666666666644912.0Zinc fingerC2HC pre-PHD-type 1%3B degenerate
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159283_33153.6666666666666644912.0Zinc fingerPHD-type 1
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159341_39153.6666666666666644912.0Zinc fingerPHD-type 2
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159344_38953.6666666666666644912.0Zinc fingerRING-type
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159388_43853.6666666666666644912.0Zinc fingerPHD-type 3
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594399_443953.6666666666666644912.0Zinc fingerC2HC pre-PHD-type 2
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-1594460_450753.6666666666666644912.0Zinc fingerPHD-type 8
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159464_52053.6666666666666644912.0Zinc fingerPHD-type 4
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000262189-159957_101053.6666666666666644912.0Zinc fingerPHD-type 5
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601007_105753.6666666666666644969.0Zinc fingerPHD-type 6
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1601084_113953.6666666666666644969.0Zinc fingerPHD-type 7
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160227_26253.6666666666666644969.0Zinc fingerC2HC pre-PHD-type 1%3B degenerate
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160283_33153.6666666666666644969.0Zinc fingerPHD-type 1
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160341_39153.6666666666666644969.0Zinc fingerPHD-type 2
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160344_38953.6666666666666644969.0Zinc fingerRING-type
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160388_43853.6666666666666644969.0Zinc fingerPHD-type 3
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604399_443953.6666666666666644969.0Zinc fingerC2HC pre-PHD-type 2
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-1604460_450753.6666666666666644969.0Zinc fingerPHD-type 8
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160464_52053.6666666666666644969.0Zinc fingerPHD-type 4
HgeneKMT2Cchr7:152132711chr7:127447538ENST00000355193-160957_101053.6666666666666644969.0Zinc fingerPHD-type 5
TgeneSND1chr7:152132711chr7:127447538ENST0000035472592418_166384.0911.0DomainTNase-like 1
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924193_328384.0911.0DomainTNase-like 2
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924341_496384.0911.0DomainTNase-like 3
TgeneSND1chr7:152132711chr7:127447538ENST00000354725924321_325384.0911.0MotifNuclear localization signal


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>1114_KMT2C_152132711_SND1_127447538_1114_KMT2C_152132711_SND1_127447538_ranked_0.pdbKMT2C152132711152132711ENST00000354725SND1chr7127447538+
MRPLYDIPYMFEAREFLRKKLIGKKVNVTVDYIRPASPATETVPAFSERTCATVTIGGINIAEALVSKGLATVIRYRQDDDQRSSHYDEL
LAAEARAIKNGKGLHSKKEVPIHRVADISGDTQKAKQFLPFLQRAGRSEAVVEYVFSGSRLKLYLPKETCLITFLLAGIECPRGARNLPG
LVQEGEPFSEEATLFTKELVLQREVEVEVESMDKAGNFIGWLHIDGANLSVLLVEHALSKVHFTAERSSYYKSLLSAEEAAKQKKEKVWA
HYEEQPVEEVMPVLEEKERSASYKPVFVTEITDDLHFYVQDVETGTQLEKLMENMRNDIASHPPVEGSYAPRRGEFCIAKFVDGEWYRAR
VEKVESPAKIHVFYIDYGNREVLPSTRLGTLSPAFSTRVLPAQATEYAFAFIQVPQDDDARTDAVDSVVRDIQNTQCLLNVEHLSAGCPH
521


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
KMT2C_pLDDT.png
all structure
all structure
SND1_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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
SND1IKBKE, SNW1, RBPJ, GTF2E2, GTF2E1, MYB, PIM1, STAT6, POLR2A, USP22, PDPK1, PRKAA1, UBA5, LZTR1, DHX9, CREBBP, RBM39, SIRT7, HHV8GK18_gp81, CUL3, CDK2, CAND1, APP, RPS3, HNRNPM, TOMM22, RPL19, MYBBP1A, SMNDC1, RPS20, NENF, RPL4, VDAC2, ILF2, SRSF3, HNRNPU, RPN1, HNRNPR, SSR3, FN1, VCAM1, CSNK2A1, ITGA4, G3BP1, PRPF8, RNU1-1, RNU2-1, RNU4-1, RNU6-1, RNU5A-1, MAK, TARDBP, EIF3CL, RPS11, RPS2, RPS6, RPS9, DDX3X, RPL23A, RPL35, RPS16, RPS26, RPS27, RPS3A, SHFM1, LIN28A, HUWE1, RAPGEF2, MDM2, CUL7, OBSL1, CCDC8, UBE2I, ESR1, MMP28, TDRD3, TXNDC5, NTRK1, NPM1, RPL10, CNOT1, Eif3a, Pabpc1, Rpl35, Srp72, Rrbp1, MCM2, U2AF2, CDH1, PTP4A1, MTDH, PA2G4, TRAP1, ANXA5, SNRPB2, EIF5B, GPI, IDH2, PDIA3, UBE2N, MRPL12, CRNN, ZNF207, CPNE3, CS, PYGL, SF3A3, DNAJC8, PLS3, CPSF6, NANS, SF3A1, ECHS1, SRP68, MYL12B, AIMP1, CYLD, DLD, DLST, PDHA1, SOD1, TRIM25, BRCA1, YAP1, EFTUD2, AAR2, PIH1D1, CHD3, ESR2, HEXIM1, AGR2, RECQL4, WWP1, MYC, CANX, GRWD1, KIAA1429, ATG16L1, NR2C2, AGRN, BMH2, BMH1, BRF1, AASS, P4HA1, HSP90AA1, HSP90AB1, LRPPRC, HADHA, ATP5C1, SHMT2, MCFD2, ATP5F1, VCP, CTNNB1, BCAP31, DLAT, EPRS, ILF3, PARP1, SFPQ, ALDH16A1, BCL2L13, CCT7, CORO1C, GFM1, PNPT1, SQSTM1, MAB21L2, SNRNP70, GSK3B, ANO7, BIRC3, STAU1, LMBR1L, NFX1, WWP2, Hsp22, TRIM28, PLEKHA4, PINK1, HCVgp1, ZC3H18, FGFR1, EMC4, HNRNPC, M, nsp4, nsp6, nsp8, ORF7b, CAPRIN1, LARP4B, MEX3B, SYNCRIP, TOP3B, UNK, USP10, SDCCAG3, CIT, ANLN, PTGER4, KIF14, FKBP8, PTPN1, ORF9b, LRRC59, SUMO2, NDN, HULC, NUPR1, BRD4, Apc2, LGALS9, IFI16, BKRF1, ASXL1, DNAJC1, DNAJC25, SEC63, H2AFX, TFDP1, MAX, LINC00624, CD274, ISG15, UFL1, DDRGK1, TP53, CKAP4, ELOVL5, EMD, GORASP1, MAPRE1, METTL7A, RPS24, SEC61B, SEC62, SERBP1, SSR1, STIM1, STX4, TMPO, FZR1, HOXA1, NAA40, BGLT3, PSMC3, ARFGAP1, PRPS2, SPINT2, FAM221B, BDH2, SYT6, EP300, CTIF, RCHY1, CCNF, MAP1LC3B, SLFN11, PDE4B, SIRT6,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
KMT2C
SND1all structure


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


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Related Drugs to KMT2C-SND1


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 KMT2C-SND1


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
TgeneSND1C0004352Autistic Disorder1CTD_human
TgeneSND1C0024121Lung Neoplasms1CTD_human
TgeneSND1C0242379Malignant neoplasm of lung1CTD_human