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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: 18145

FusionGeneSummary for KANSL1_ORMDL3

check button Fusion gene summary
Fusion gene informationFusion gene name: KANSL1_ORMDL3
Fusion gene ID: 18145
HgeneTgene
Gene symbol

KANSL1

ORMDL3

Gene ID

284058

94103

Gene nameKAT8 regulatory NSL complex subunit 1ORMDL sphingolipid biosynthesis regulator 3
SynonymsCENP-36|KDVS|KIAA1267|MSL1v1|NSL1|hMSL1v1-
Cytomap

17q21.31

17q21.1

Type of geneprotein-codingprotein-coding
DescriptionKAT8 regulatory NSL complex subunit 1MLL1/MLL complex subunit KANSL1MSL1 homolog 1NSL complex protein NSL1centromere protein 36male-specific lethal 1 homolognon-specific lethal 1 homologORM1-like protein 3
Modification date2018052320180523
UniProtAcc

Q7Z3B3

Q8N138

Ensembl transtripts involved in fusion geneENST00000574590, ENST00000575318, 
ENST00000572904, ENST00000262419, 
ENST00000432791, ENST00000393476, 
ENST00000576248, 
ENST00000304046, 
ENST00000579695, ENST00000394169, 
ENST00000584220, ENST00000582052, 
Fusion gene scores* DoF score18 X 14 X 7=17646 X 2 X 5=60
# samples 196
** MAII scorelog2(19/1764*10)=-3.21477923722657
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/60*10)=0
Context

PubMed: KANSL1 [Title/Abstract] AND ORMDL3 [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
HgeneKANSL1

GO:0043981

histone H4-K5 acetylation

20018852

HgeneKANSL1

GO:0043982

histone H4-K8 acetylation

20018852

HgeneKANSL1

GO:0043984

histone H4-K16 acetylation

20018852


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
TCGALDBRCATCGA-AC-A23H-01AKANSL1chr17

44144915

-ORMDL3chr17

38080478

-
* 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-5UTRENST00000574590ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000574590ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000574590ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000574590ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000574590ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000575318ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000575318ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000575318ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000575318ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000575318ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000572904ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000572904ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000572904ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000572904ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000572904ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000262419ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000262419ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000262419ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000262419ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000262419ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000432791ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000432791ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-5UTRENST00000432791ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000432791ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5CDS-intronENST00000432791ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5UTR-5UTRENST00000393476ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5UTR-5UTRENST00000393476ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5UTR-5UTRENST00000393476ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5UTR-intronENST00000393476ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
5UTR-intronENST00000393476ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
intron-5UTRENST00000576248ENST00000304046KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
intron-5UTRENST00000576248ENST00000579695KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
intron-5UTRENST00000576248ENST00000394169KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
intron-intronENST00000576248ENST00000584220KANSL1chr17

44144915

-ORMDL3chr17

38080478

-
intron-intronENST00000576248ENST00000582052KANSL1chr17

44144915

-ORMDL3chr17

38080478

-

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FusionProtFeatures for KANSL1_ORMDL3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KANSL1

Q7Z3B3

ORMDL3

Q8N138

Negative regulator of sphingolipid synthesis. Mayindirectly regulate endoplasmic reticulum-mediated Ca(+2)signaling. {ECO:0000269|PubMed:20182505}.

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 KANSL1_ORMDL3


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 KANSL1_ORMDL3


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
KANSL1CCDC85B, KRT15, NINL, PSME3, TRAF2, NECAB2, CEP70, USHBP1, CALCOCO2, PLEKHA5, KAT8, WDR5, CDC5L, DISC1, EXOC1, RBBP5, DHX8, CTCF, SMAD3, KDM1A, CDR2, GOLGA2, KIFC3, MAGEA12, TRIM27, PNMA1, TRAF4, SPAG5, NUP62, TFIP11, HOOK2, CCDC136, DTNBP1, FSD2, NUTM1, HSPB1, MDFI, FOXK2, PHF20, PHF20L1, KANSL2, TRAF1, DUS2, MCRS1, ECI2, TPM2, TRIM25ORMDL3EEF1A1, SPTLC1, ELAVL1, LNX1, APP, TCTN3, SLC1A1, SLC22A9, SPRY4, SLC2A12, PTPN11, LMNA


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 KANSL1_ORMDL3


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 KANSL1_ORMDL3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneKANSL1C0026827Muscle hypotonia2CTD_human
HgeneKANSL1C0376634Craniofacial Abnormalities2CTD_human
HgeneKANSL1C2931713Chromosome 17 deletion2CTD_human
HgeneKANSL1C3714756Intellectual Disability2CTD_human
HgeneKANSL1C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneKANSL1C1860789Leukemia, Megakaryoblastic, of Down Syndrome1CTD_human
TgeneORMDL3C0004096Asthma2CTD_human
TgeneORMDL3C0009324Ulcerative Colitis1CTD_human