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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: 16502

FusionGeneSummary for HN1L_WDR18

check button Fusion gene summary
Fusion gene informationFusion gene name: HN1L_WDR18
Fusion gene ID: 16502
HgeneTgene
Gene symbol

HN1L

WDR18

Gene ID

57585

57418

Gene namecramped chromatin regulator homolog 1WD repeat domain 18
SynonymsCRAMP1L|HN1L|TCE4Ipi3|R32184_1
Cytomap

16p13.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionprotein cramped-likeCrm, cramped-likeT-complex expressed gene 4hematological and neurological expressed 1-like proteinWD repeat-containing protein 18Involved in Processing ITS2 3 homolog
Modification date2018052320180523
UniProtAcc

Q9BV38

Ensembl transtripts involved in fusion geneENST00000569256, ENST00000248098, 
ENST00000562684, ENST00000561516, 
ENST00000382711, ENST00000569765, 
ENST00000382710, 
ENST00000591997, 
ENST00000251289, ENST00000587001, 
Fusion gene scores* DoF score6 X 6 X 2=725 X 3 X 5=75
# samples 75
** MAII scorelog2(7/72*10)=-0.0406419844973459
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HN1L [Title/Abstract] AND WDR18 [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

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
TCGALDLUSCTCGA-NC-A5HE-01AHN1Lchr16

1749048

+WDR18chr19

989762

+
* 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
3UTR-3UTRENST00000569256ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000569256ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000569256ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000248098ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000248098ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000248098ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000562684ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000562684ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000562684ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000561516ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000561516ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000561516ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382711ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382711ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382711ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000569765ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000569765ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000569765ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382710ENST00000591997HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382710ENST00000251289HN1Lchr16

1749048

+WDR18chr19

989762

+
3UTR-3UTRENST00000382710ENST00000587001HN1Lchr16

1749048

+WDR18chr19

989762

+

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FusionProtFeatures for HN1L_WDR18


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HN1L

WDR18

Q9BV38

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Functions as a component of the Five Friends ofMethylated CHTOP (5FMC) complex; the 5FMC complex is recruited toZNF148 by methylated CHTOP, leading to desumoylation of ZNF148 andsubsequent transactivation of ZNF148 target genes(PubMed:22872859). Component of the PELP1 complex involved in thenucleolar steps of 28S rRNA maturation and the subsequentnucleoplasmic transit of the pre-60S ribosomal subunit(PubMed:21326211). {ECO:0000269|PubMed:21326211,ECO:0000269|PubMed:22872859}.

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 HN1L_WDR18


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 HN1L_WDR18


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
HN1LCSNK1D, SEPT2, CNTFR, LMNA, EGR2, WWOX, HSPB1, STMN1, UBA5, U2AF2, CDH1, FIGNL1, CARM1, YAP1, TESWDR18USP42, CSNK2B, TK1, SMN1, ANXA7, SMARCAD1, SIRT7, CUL3, SF3B3, HNRNPU, EIF4A3, HNRNPC, CDC5L, SAP18, LMNA, UTP14A, NHP2L1, SF3B6, NCSTN, VTN, IK, RFC1, SRSF1, ESR1, MDC1, PAXIP1, LAS1L, PELP1, MOK, GPRASP2, SHMT2, MOV10, CUL7, OBSL1, SENP3, ISCA1, NOL9, TEX10, ACOT2, CHD8, IFI16, NPM1, KIF2C, EXOSC4, FOXQ1, FOXS1, SNW1, DUSP22


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 HN1L_WDR18


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 HN1L_WDR18


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