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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: 19108

FusionGeneSummary for KMT2A_SLC22A10

check button Fusion gene summary
Fusion gene informationFusion gene name: KMT2A_SLC22A10
Fusion gene ID: 19108
HgeneTgene
Gene symbol

KMT2A

SLC22A10

Gene ID

4297

387775

Gene namelysine methyltransferase 2Asolute carrier family 22 member 10
SynonymsALL-1|CXXC7|HRX|HTRX1|MLL|MLL1|MLL1A|TRX1|WDSTSOAT5|hOAT5
Cytomap

11q23.3

11q12.3

Type of geneprotein-codingprotein-coding
Descriptionhistone-lysine N-methyltransferase 2ACXXC-type zinc finger protein 7lysine (K)-specific methyltransferase 2Alysine N-methyltransferase 2Amixed lineage leukemia 1myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila)trithorax-likesolute carrier family 22 member 10organic anion transporter 5solute carrier family 22 (organic anion/cation transporter), member 10
Modification date2018051920180522
UniProtAcc

Q03164

Q63ZE4

Ensembl transtripts involved in fusion geneENST00000534358, ENST00000389506, 
ENST00000354520, ENST00000420751, 
ENST00000525620, ENST00000535888, 
ENST00000544661, ENST00000332793, 
ENST00000526800, 
Fusion gene scores* DoF score31 X 72 X 6=133924 X 4 X 4=64
# samples 1294
** MAII scorelog2(129/13392*10)=-3.37592846223973
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KMT2A [Title/Abstract] AND SLC22A10 [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
HgeneKMT2A

GO:0045944

positive regulation of transcription by RNA polymerase II

20861184

HgeneKMT2A

GO:0051568

histone H3-K4 methylation

19556245

HgeneKMT2A

GO:0065003

protein-containing complex assembly

15199122

HgeneKMT2A

GO:0080182

histone H3-K4 trimethylation

20861184


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
TCGALDBLCATCGA-BT-A2LA-01AKMT2Achr11

118345030

+SLC22A10chr11

63129852

+
* 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-3UTRENST00000534358ENST00000525620KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-3UTRENST00000534358ENST00000535888KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000534358ENST00000544661KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000534358ENST00000332793KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000534358ENST00000526800KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-3UTRENST00000389506ENST00000525620KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-3UTRENST00000389506ENST00000535888KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000389506ENST00000544661KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000389506ENST00000332793KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000389506ENST00000526800KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-3UTRENST00000354520ENST00000525620KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-3UTRENST00000354520ENST00000535888KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000354520ENST00000544661KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000354520ENST00000332793KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
5CDS-intronENST00000354520ENST00000526800KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
intron-3UTRENST00000420751ENST00000525620KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
intron-3UTRENST00000420751ENST00000535888KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
intron-intronENST00000420751ENST00000544661KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
intron-intronENST00000420751ENST00000332793KMT2Achr11

118345030

+SLC22A10chr11

63129852

+
intron-intronENST00000420751ENST00000526800KMT2Achr11

118345030

+SLC22A10chr11

63129852

+

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FusionProtFeatures for KMT2A_SLC22A10


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KMT2A

Q03164

SLC22A10

Q63ZE4


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 KMT2A_SLC22A10


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 KMT2A_SLC22A10


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
KMT2APPIE, PPP1R15A, KMT2A, ASH2L, HCFC1, HCFC2, MEN1, RBBP5, WDR5, AVP, INS, OXT, MAP3K5, HDAC1, CTBP1, CBX4, BMI1, CREBBP, SMARCB1, CXXC1, MYB, CTNNB1, SNW1, E2F2, E2F4, E2F6, PSIP1, MLLT4, POLR2A, KAT8, RNF2, TP53, SBF1, MTM1, SET, HIST1H3A, HIST1H4A, KAT6A, ELL, AFF1, AFF4, CDK9, CCNT1, CTR9, LEO1, PAF1, CDC73, WDR61, MLLT3, DOT1L, SKP2, HIST3H3, SVIL, HIST2H3C, SIN3A, MLLT1, RUNX1, CBFB, H3F3A, SIRT7, ASB2, TCEB1, TCEB2, CBX8, TOP1, TAF6, NCL, HECW2, LGR4, CSNK2A2, SENP3, SYMPK, PKN1, PIH1D1, KRAS, TAF1, CHD3, SMARCA2, SMARCC2, SMARCC1, HDAC2, RBBP4, RBBP7, TBP, MBD3, SAP30, RAN, TAF9, TASP1, HIST1H2BG, EWSR1, DYNLT1, KIF11, ING4, ZNF131, ASB7SLC22A10


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 KMT2A_SLC22A10


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 KMT2A_SLC22A10


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneKMT2AC0023418leukemia2CTD_human
HgeneKMT2AC0023467Leukemia, Myelocytic, Acute2CTD_human
HgeneKMT2AC0023470Myeloid Leukemia2CTD_human
HgeneKMT2AC1961102Precursor Cell Lymphoblastic Leukemia Lymphoma2CTD_human
HgeneKMT2AC0001418Adenocarcinoma1CTD_human
HgeneKMT2AC0005695Bladder Neoplasm1CTD_human
HgeneKMT2AC0007138Carcinoma, Transitional Cell1CTD_human
HgeneKMT2AC0008625Chromosome Aberrations1CTD_human
HgeneKMT2AC0023448Lymphoid leukemia1CTD_human
HgeneKMT2AC0023465Acute monocytic leukemia1CTD_human
HgeneKMT2AC0023479Acute myelomonocytic leukemia1CTD_human
HgeneKMT2AC0036341Schizophrenia1PSYGENET
HgeneKMT2AC0038356Stomach Neoplasms1CTD_human
HgeneKMT2AC0149925Small cell carcinoma of lung1CTD_human
HgeneKMT2AC2239176Liver carcinoma1CTD_human