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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: 6962

FusionGeneSummary for CHD1_RGMB

check button Fusion gene summary
Fusion gene informationFusion gene name: CHD1_RGMB
Fusion gene ID: 6962
HgeneTgene
Gene symbol

CHD1

RGMB

Gene ID

1105

285704

Gene namechromodomain helicase DNA binding protein 1repulsive guidance molecule BMP co-receptor b
SynonymsPILBOSDRAGON
Cytomap

5q15-q21.1

5q15

Type of geneprotein-codingprotein-coding
Descriptionchromodomain-helicase-DNA-binding protein 1ATP-dependent helicase CHD1CHD-1RGM domain family member BDRG11-responsive axonal guidance and outgrowth of neuriteRGM domain family, member Brepulsive guidance molecule Brepulsive guidance molecule family member b
Modification date2018052220180523
UniProtAcc

O14646

Q6NW40

Ensembl transtripts involved in fusion geneENST00000284049, ENST00000511067, 
ENST00000504776, ENST00000308234, 
ENST00000513185, 
Fusion gene scores* DoF score6 X 7 X 5=2101 X 1 X 1=1
# samples 72
** MAII scorelog2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/1*10)=4.32192809488736
Context

PubMed: CHD1 [Title/Abstract] AND RGMB [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
TCGARVCOADTCGA-DM-A288-01ACHD1chr5

98215256

-RGMBchr5

98128789

+
TCGALDCOADTCGA-A6-6648-01ACHD1chr5

98204199

-RGMBchr5

98128789

+
* 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-intronENST00000284049ENST00000504776CHD1chr5

98215256

-RGMBchr5

98128789

+
5CDS-intronENST00000284049ENST00000308234CHD1chr5

98215256

-RGMBchr5

98128789

+
5CDS-intronENST00000284049ENST00000513185CHD1chr5

98215256

-RGMBchr5

98128789

+
intron-intronENST00000511067ENST00000504776CHD1chr5

98215256

-RGMBchr5

98128789

+
intron-intronENST00000511067ENST00000308234CHD1chr5

98215256

-RGMBchr5

98128789

+
intron-intronENST00000511067ENST00000513185CHD1chr5

98215256

-RGMBchr5

98128789

+
5CDS-intronENST00000284049ENST00000504776CHD1chr5

98204199

-RGMBchr5

98128789

+
5CDS-intronENST00000284049ENST00000308234CHD1chr5

98204199

-RGMBchr5

98128789

+
5CDS-intronENST00000284049ENST00000513185CHD1chr5

98204199

-RGMBchr5

98128789

+
5UTR-intronENST00000511067ENST00000504776CHD1chr5

98204199

-RGMBchr5

98128789

+
5UTR-intronENST00000511067ENST00000308234CHD1chr5

98204199

-RGMBchr5

98128789

+
5UTR-intronENST00000511067ENST00000513185CHD1chr5

98204199

-RGMBchr5

98128789

+

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FusionProtFeatures for CHD1_RGMB


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CHD1

O14646

RGMB

Q6NW40

ATP-dependent chromatin-remodeling factor whichfunctions as substrate recognition component of the transcriptionregulatory histone acetylation (HAT) complex SAGA. Regulatespolymerase II transcription. Also required for efficienttranscription by RNA polymerase I, and more specifically thepolymerase I transcription termination step. Regulates negativelyDNA replication. Not only involved in transcription-relatedchromatin-remodeling, but also required to maintain a specificchromatin configuration across the genome. Is also associated withhistone deacetylase (HDAC) activity (By similarity). Required forthe bridging of SNF2, the FACT complex, the PAF complex as well asthe U2 snRNP complex to H3K4me3. Functions to modulate theefficiency of pre-mRNA splicing in part through physical bridgingof spliceosomal components to H3K4me3 (PubMed:18042460,PubMed:28866611). Required for maintaining open chromatin andpluripotency in embryonic stem cells (By similarity).{ECO:0000250|UniProtKB:P40201, ECO:0000269|PubMed:18042460,ECO:0000269|PubMed:28866611}. Member of the repulsive guidance molecule (RGM) familythat contributes to the patterning of the developing nervoussystem (By similarity). Acts as a bone morphogenetic protein (BMP)coreceptor that potentiates BMP signaling (By similarity).Promotes neuronal adhesion (By similarity). May inhibit neuriteoutgrowth. {ECO:0000250, ECO:0000269|PubMed:19324014}.

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 CHD1_RGMB


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 CHD1_RGMB


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
CHD1ARRB1, HDAC1, BCLAF1, SRSF3, NCOR1, SAFB, SSRP1, CEBPA, HMGA1, HIST1H3A, MLLT1, PAF1, ELAVL1, SIRT7, ISG15, SPP1, FBXW11, HIST3H3, CUL7, OBSL1, NTRK1, CTR9, RTF1, HNRNPU, NPM1, RPL10, TMPO, BTRC, INO80B, RNF157RGMB


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 CHD1_RGMB


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneCHD1O14646DB00445EpirubicinChromodomain-helicase-DNA-binding protein 1small moleculeapproved

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RelatedDiseases for CHD1_RGMB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneRGMBC0003873Rheumatoid Arthritis1CTD_human