UTHEALTH HOME ABOUT SBMI A-Z WEBMAIL INSIDE THE UNIVERSITY |
|
Fusion Protein:KMT2C-AUTS2 |
Fusion Protein Summary |
Fusion gene summary |
Fusion partner gene information | Fusion gene name: KMT2C-AUTS2 | FusionPDB ID: 43235 | FusionGDB2.0 ID: 54197 | Hgene | Tgene | Gene symbol | KMT2C | AUTS2 | Gene ID | 58508 | 26053 |
Gene name | lysine methyltransferase 2C | activator of transcription and developmental regulator AUTS2 | |
Synonyms | HALR|KLEFS2|MLL3 | FBRSL2|MRD26 | |
Cytomap | 7q36.1 | 7q11.22 | |
Type of gene | protein-coding | protein-coding | |
Description | histone-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 le | autism susceptibility gene 2 proteinAUTS2, activator of transcription and developmental regulatorautism susceptibility candidate 2autism-related protein 1 | |
Modification date | 20200320 | 20200313 | |
UniProtAcc | Q8NEZ4 | Q8WXX7 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000262189, ENST00000355193, ENST00000485241, ENST00000485655, | ENST00000403018, ENST00000489774, ENST00000342771, ENST00000406775, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 26 X 23 X 12=7176 | 25 X 24 X 10=6000 |
# samples | 32 | 27 | |
** MAII score | log2(32/7176*10)=-4.4870360800319 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(27/6000*10)=-4.47393118833241 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 AUTS2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | KMT2C(152132711)-AUTS2(69900738), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | KMT2C-AUTS2 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-AUTS2 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-AUTS2 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-AUTS2 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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | KMT2C | GO:0097692 | histone H3-K4 monomethylation | 26324722 |
Tgene | AUTS2 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 25519132 |
Tgene | AUTS2 | GO:0051571 | positive regulation of histone H3-K4 methylation | 25519132 |
Tgene | AUTS2 | GO:2000620 | positive regulation of histone H4-K16 acetylation | 25519132 |
Fusion 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. |
Fusion gene breakpoints across AUTS2 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Top |
Fusion Gene Sample Information |
Fusion gene information from FusionGDB2.0. |
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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | BRCA | TCGA-A8-A07C-01A | KMT2C | chr7 | 152132711 | - | AUTS2 | chr7 | 69900738 | + |
Top |
Fusion ORF Analysis |
Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000262189 | KMT2C | chr7 | 152132711 | - | ENST00000406775 | AUTS2 | chr7 | 69900738 | + | 4935 | 380 | 689 | 3427 | 912 |
ENST00000262189 | KMT2C | chr7 | 152132711 | - | ENST00000342771 | AUTS2 | chr7 | 69900738 | + | 5572 | 380 | 689 | 3499 | 936 |
ENST00000355193 | KMT2C | chr7 | 152132711 | - | ENST00000406775 | AUTS2 | chr7 | 69900738 | + | 4935 | 380 | 689 | 3427 | 912 |
ENST00000355193 | KMT2C | chr7 | 152132711 | - | ENST00000342771 | AUTS2 | chr7 | 69900738 | + | 5572 | 380 | 689 | 3499 | 936 |
DeepORF 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. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000262189 | ENST00000406775 | KMT2C | chr7 | 152132711 | - | AUTS2 | chr7 | 69900738 | + | 0.008703251 | 0.99129677 |
ENST00000262189 | ENST00000342771 | KMT2C | chr7 | 152132711 | - | AUTS2 | chr7 | 69900738 | + | 0.006319878 | 0.9936801 |
ENST00000355193 | ENST00000406775 | KMT2C | chr7 | 152132711 | - | AUTS2 | chr7 | 69900738 | + | 0.008703251 | 0.99129677 |
ENST00000355193 | ENST00000342771 | KMT2C | chr7 | 152132711 | - | AUTS2 | chr7 | 69900738 | + | 0.006319878 | 0.9936801 |
Top |
Fusion Amino Acid Sequences |
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 >43235_43235_1_KMT2C-AUTS2_KMT2C_chr7_152132711_ENST00000262189_AUTS2_chr7_69900738_ENST00000342771_length(amino acids)=936AA_BP= MVQRTEAPPQPPPLSTQPPQGPPEAQLQPAPQPQVQRPPRPQSPTQLLHQNLPPVQAHPSAQSLSQPLSAYNSSSLSLNSLSSSRSSTPA KTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVAGHPAGSTYSEQDILRQELNTRFL ASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPM IPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLK PEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNS MFGHKDGPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHSSHPSPAPVLPV NALGHTRSSTEQIRAHLNTEAREKDKPKERERDHSESRKDLAADEHKAKEGHLPEKDGHGHEGRAAGEEAKQLARVPSPYVRTPVVESAR PNSTSSREAEPRKGEPAYENPKKSSEVKVKEERKEDHDLPPEAPQTHRASEPPPPNSSSSVHPGPLASMPMTVGVTGIHPMNSISSLDRT RMMTPFMGISPLPGGERFPYPSFHWDPIRDPLRDPYRELDIHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHH PLSVDPRREHERGGHLDERERLHMLREDYEHTRLHSVHPASLDGHLPHPSLITPGLPSMHYPRISPTAGNQNGLLNKTPPTAALSAPPPL -------------------------------------------------------------- >43235_43235_2_KMT2C-AUTS2_KMT2C_chr7_152132711_ENST00000262189_AUTS2_chr7_69900738_ENST00000406775_length(amino acids)=912AA_BP= MVQRTEAPPQPPPLSTQPPQGPPEAQLQPAPQPQVQRPPRPQSPTQLLHQNLPPVQAHPSAQSLSQPLSAYNSSSLSLNSLSSSRSSTPA KTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVAGHPAGSTYSEQDILRQELNTRFL ASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPM IPPTGPFGSLQGAFQPKLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLAR PSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSMFGHKDGPSVQNFSNPHEPWNRLH RTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHSSHPSPAPVLPVNALGHTRSSTEQIRAHLNTEAREK DKPKERERDHSESRKDLAADEHKAKEGHLPEKDGHGHEGRAAGEEAKQLARVPSPYVRTPVVESARPNSTSSREAEPRKGEPAYENPKKS SEVKVKEERKEDHDLPPEAPQTHRASEPPPPNSSSSVHPGPLASMPMTVGVTGIHPMNSISSLDRTRMMTPFMGISPLPGGERFPYPSFH WDPIRDPLRDPYRELDIHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLSVDPRREHERGGHLDERERLHM LREDYEHTRLHSVHPASLDGHLPHPSLITPGLPSMHYPRISPTAGNQNGLLNKTPPTAALSAPPPLISTLGGRPVSPRRTTPLSAEIRER -------------------------------------------------------------- >43235_43235_3_KMT2C-AUTS2_KMT2C_chr7_152132711_ENST00000355193_AUTS2_chr7_69900738_ENST00000342771_length(amino acids)=936AA_BP= MVQRTEAPPQPPPLSTQPPQGPPEAQLQPAPQPQVQRPPRPQSPTQLLHQNLPPVQAHPSAQSLSQPLSAYNSSSLSLNSLSSSRSSTPA KTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVAGHPAGSTYSEQDILRQELNTRFL ASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPM IPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLK PEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNS MFGHKDGPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHSSHPSPAPVLPV NALGHTRSSTEQIRAHLNTEAREKDKPKERERDHSESRKDLAADEHKAKEGHLPEKDGHGHEGRAAGEEAKQLARVPSPYVRTPVVESAR PNSTSSREAEPRKGEPAYENPKKSSEVKVKEERKEDHDLPPEAPQTHRASEPPPPNSSSSVHPGPLASMPMTVGVTGIHPMNSISSLDRT RMMTPFMGISPLPGGERFPYPSFHWDPIRDPLRDPYRELDIHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHH PLSVDPRREHERGGHLDERERLHMLREDYEHTRLHSVHPASLDGHLPHPSLITPGLPSMHYPRISPTAGNQNGLLNKTPPTAALSAPPPL -------------------------------------------------------------- >43235_43235_4_KMT2C-AUTS2_KMT2C_chr7_152132711_ENST00000355193_AUTS2_chr7_69900738_ENST00000406775_length(amino acids)=912AA_BP= MVQRTEAPPQPPPLSTQPPQGPPEAQLQPAPQPQVQRPPRPQSPTQLLHQNLPPVQAHPSAQSLSQPLSAYNSSSLSLNSLSSSRSSTPA KTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVAGHPAGSTYSEQDILRQELNTRFL ASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPM IPPTGPFGSLQGAFQPKLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLAR PSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSMFGHKDGPSVQNFSNPHEPWNRLH RTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHSSHPSPAPVLPVNALGHTRSSTEQIRAHLNTEAREK DKPKERERDHSESRKDLAADEHKAKEGHLPEKDGHGHEGRAAGEEAKQLARVPSPYVRTPVVESARPNSTSSREAEPRKGEPAYENPKKS SEVKVKEERKEDHDLPPEAPQTHRASEPPPPNSSSSVHPGPLASMPMTVGVTGIHPMNSISSLDRTRMMTPFMGISPLPGGERFPYPSFH WDPIRDPLRDPYRELDIHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLSVDPRREHERGGHLDERERLHM LREDYEHTRLHSVHPASLDGHLPHPSLITPGLPSMHYPRISPTAGNQNGLLNKTPPTAALSAPPPLISTLGGRPVSPRRTTPLSAEIRER -------------------------------------------------------------- |
Top |
Fusion Protein Functional Features |
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/chr7:69900738) - 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. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
KMT2C | AUTS2 |
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: Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility (PubMed:25519132). The PRC1-like complex that contains PCGF5, RNF2, CSNK2B, RYBP and AUTS2 has decreased histone H2A ubiquitination activity, due to the phosphorylation of RNF2 by CSNK2B (PubMed:25519132). As a consequence, the complex mediates transcriptional activation (PubMed:25519132). In the cytoplasm, plays a role in axon and dendrite elongation and in neuronal migration during embryonic brain development. Promotes reorganization of the actin cytoskeleton, lamellipodia formation and neurite elongation via its interaction with RAC guanine nucleotide exchange factors, which then leads to the activation of RAC1 (By similarity). {ECO:0000250|UniProtKB:A0A087WPF7, ECO:0000269|PubMed:25519132}. |
Retention 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 * Minus value of BPloci means that the break pointn is located before the CDS. |
- Retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 34_46 | 53.666666666666664 | 4912.0 | DNA binding | Note=A.T hook |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 34_46 | 53.666666666666664 | 4969.0 | DNA binding | Note=A.T hook |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000342771 | 3 | 19 | 1122_1181 | 220.0 | 1260.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000342771 | 3 | 19 | 288_471 | 220.0 | 1260.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000342771 | 3 | 19 | 525_548 | 220.0 | 1260.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000342771 | 3 | 19 | 545_646 | 220.0 | 1260.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000403018 | 0 | 5 | 1122_1181 | 0 | 267.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000403018 | 0 | 5 | 288_471 | 0 | 267.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000403018 | 0 | 5 | 525_548 | 0 | 267.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000403018 | 0 | 5 | 545_646 | 0 | 267.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000406775 | 3 | 18 | 1122_1181 | 220.0 | 1236.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000406775 | 3 | 18 | 288_471 | 220.0 | 1236.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000406775 | 3 | 18 | 525_548 | 220.0 | 1236.0 | Compositional bias | His-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000406775 | 3 | 18 | 545_646 | 220.0 | 1236.0 | Compositional bias | Pro-rich | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000342771 | 3 | 19 | 289_472 | 220.0 | 1260.0 | Region | Important for regulation of lamellipodia formation | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000403018 | 0 | 5 | 289_472 | 0 | 267.0 | Region | Important for regulation of lamellipodia formation | |
Tgene | AUTS2 | chr7:152132711 | chr7:69900738 | ENST00000406775 | 3 | 18 | 289_472 | 220.0 | 1236.0 | Region | Important for regulation of lamellipodia formation |
- Not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1338_1366 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1754_1787 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 3054_3081 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 3173_3272 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 3391_3433 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 644_672 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 92_112 | 53.666666666666664 | 4912.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1338_1366 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1754_1787 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 3054_3081 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 3173_3272 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 3391_3433 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 644_672 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 92_112 | 53.666666666666664 | 4969.0 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1719_1796 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Gln-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1834_2281 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 2412_2630 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 2690_2786 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Asp-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 3012_3509 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Gln-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 3277_3381 | 53.666666666666664 | 4912.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1719_1796 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Gln-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1834_2281 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 2412_2630 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 2690_2786 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Asp-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 3012_3509 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Gln-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 3277_3381 | 53.666666666666664 | 4969.0 | Compositional bias | Note=Pro-rich |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 436_489 | 53.666666666666664 | 4912.0 | Domain | DHHC |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4545_4605 | 53.666666666666664 | 4912.0 | Domain | FYR N-terminal |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4606_4691 | 53.666666666666664 | 4912.0 | Domain | FYR C-terminal |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4771_4887 | 53.666666666666664 | 4912.0 | Domain | SET |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4895_4911 | 53.666666666666664 | 4912.0 | Domain | Post-SET |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 436_489 | 53.666666666666664 | 4969.0 | Domain | DHHC |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4545_4605 | 53.666666666666664 | 4969.0 | Domain | FYR N-terminal |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4606_4691 | 53.666666666666664 | 4969.0 | Domain | FYR C-terminal |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4771_4887 | 53.666666666666664 | 4969.0 | Domain | SET |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4895_4911 | 53.666666666666664 | 4969.0 | Domain | Post-SET |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4848_4849 | 53.666666666666664 | 4912.0 | Region | S-adenosyl-L-methionine binding |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4848_4849 | 53.666666666666664 | 4969.0 | Region | S-adenosyl-L-methionine binding |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1007_1057 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 6 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 1084_1139 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 7 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 227_262 | 53.666666666666664 | 4912.0 | Zinc finger | C2HC pre-PHD-type 1%3B degenerate |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 283_331 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 1 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 341_391 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 2 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 344_389 | 53.666666666666664 | 4912.0 | Zinc finger | RING-type |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 388_438 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 3 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4399_4439 | 53.666666666666664 | 4912.0 | Zinc finger | C2HC pre-PHD-type 2 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 4460_4507 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 8 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 464_520 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 4 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000262189 | - | 1 | 59 | 957_1010 | 53.666666666666664 | 4912.0 | Zinc finger | PHD-type 5 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1007_1057 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 6 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 1084_1139 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 7 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 227_262 | 53.666666666666664 | 4969.0 | Zinc finger | C2HC pre-PHD-type 1%3B degenerate |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 283_331 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 1 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 341_391 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 2 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 344_389 | 53.666666666666664 | 4969.0 | Zinc finger | RING-type |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 388_438 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 3 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4399_4439 | 53.666666666666664 | 4969.0 | Zinc finger | C2HC pre-PHD-type 2 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 4460_4507 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 8 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 464_520 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 4 |
Hgene | KMT2C | chr7:152132711 | chr7:69900738 | ENST00000355193 | - | 1 | 60 | 957_1010 | 53.666666666666664 | 4969.0 | Zinc finger | PHD-type 5 |
Top |
Fusion Protein-Protein Interaction |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160) |
Gene | PPI interactors |
Protein-protein interactors based on sequence similarity (STRING) |
Gene | STRING network |
KMT2C | |
AUTS2 |
- Retained interactions in fusion protein (protein functional feature from UniProt). |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost interactions due to fusion (protein functional feature from UniProt). |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
Related Drugs to KMT2C-AUTS2 |
Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
Top |
Related Diseases to KMT2C-AUTS2 |
Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |