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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: 8912

FusionGeneSummary for CTSH_RASGRF1

check button Fusion gene summary
Fusion gene informationFusion gene name: CTSH_RASGRF1
Fusion gene ID: 8912
HgeneTgene
Gene symbol

CTSH

RASGRF1

Gene ID

1512

5923

Gene namecathepsin HRas protein specific guanine nucleotide releasing factor 1
SynonymsACC-4|ACC-5|ACC4|ACC5|CPSBCDC25|CDC25L|GNRP|GRF1|GRF55|H-GRF55|PP13187|ras-GRF1
Cytomap

15q25.1

15q25.1

Type of geneprotein-codingprotein-coding
Descriptionpro-cathepsin HN-benzoylarginine-beta-naphthylamide hydrolasealeuraincathepsin B3cathepsin BAras-specific guanine nucleotide-releasing factor 1Ras-specific guanine nucleotide-releasing factor, CDC25 homologRas-specific nucleotide exchange factor CDC25guanine nucleotide exchange factorguanine nucleotide-releasing factor 1guanine nucleotide-re
Modification date2018052320180519
UniProtAcc

P09668

Q13972

Ensembl transtripts involved in fusion geneENST00000220166, ENST00000534533, 
ENST00000558480, ENST00000419573, 
ENST00000560334, ENST00000394745, 
Fusion gene scores* DoF score2 X 3 X 3=183 X 4 X 3=36
# samples 33
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/36*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CTSH [Title/Abstract] AND RASGRF1 [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
HgeneCTSH

GO:0002764

immune response-regulating signaling pathway

16822283

HgeneCTSH

GO:0006508

proteolysis

6203523|8811434

HgeneCTSH

GO:0010628

positive regulation of gene expression

21217776

HgeneCTSH

GO:0010813

neuropeptide catabolic process

15127951

HgeneCTSH

GO:0010815

bradykinin catabolic process

15127951

HgeneCTSH

GO:0010952

positive regulation of peptidase activity

20435891

HgeneCTSH

GO:0030335

positive regulation of cell migration

21217776

HgeneCTSH

GO:0031638

zymogen activation

20435891

HgeneCTSH

GO:0033619

membrane protein proteolysis

14766755

HgeneCTSH

GO:0043129

surfactant homeostasis

18216060

HgeneCTSH

GO:0070371

ERK1 and ERK2 cascade

21217776


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
TCGARVBRCATCGA-D8-A27R-01ACTSHchr15

79221754

-RASGRF1chr15

79254578

-
TCGARVLUADTCGA-86-8056-01ACTSHchr15

79237233

-RASGRF1chr15

79320201

-
* 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
Frame-shiftENST00000220166ENST00000558480CTSHchr15

79221754

-RASGRF1chr15

79254578

-
Frame-shiftENST00000220166ENST00000419573CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5CDS-intronENST00000220166ENST00000560334CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5CDS-intronENST00000220166ENST00000394745CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5UTR-3CDSENST00000534533ENST00000558480CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5UTR-3CDSENST00000534533ENST00000419573CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5UTR-intronENST00000534533ENST00000560334CTSHchr15

79221754

-RASGRF1chr15

79254578

-
5UTR-intronENST00000534533ENST00000394745CTSHchr15

79221754

-RASGRF1chr15

79254578

-
Frame-shiftENST00000220166ENST00000558480CTSHchr15

79237233

-RASGRF1chr15

79320201

-
Frame-shiftENST00000220166ENST00000419573CTSHchr15

79237233

-RASGRF1chr15

79320201

-
5CDS-5UTRENST00000220166ENST00000560334CTSHchr15

79237233

-RASGRF1chr15

79320201

-
5CDS-intronENST00000220166ENST00000394745CTSHchr15

79237233

-RASGRF1chr15

79320201

-
intron-3CDSENST00000534533ENST00000558480CTSHchr15

79237233

-RASGRF1chr15

79320201

-
intron-3CDSENST00000534533ENST00000419573CTSHchr15

79237233

-RASGRF1chr15

79320201

-
intron-5UTRENST00000534533ENST00000560334CTSHchr15

79237233

-RASGRF1chr15

79320201

-
intron-intronENST00000534533ENST00000394745CTSHchr15

79237233

-RASGRF1chr15

79320201

-

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FusionProtFeatures for CTSH_RASGRF1


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

P09668

RASGRF1

Q13972

Important for the overall degradation of proteins inlysosomes. Promotes the exchange of Ras-bound GDP by GTP.{ECO:0000269|PubMed:11389730}.

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 CTSH_RASGRF1


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 CTSH_RASGRF1


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
CTSHCSTA, CSTB, XRN1, SLC25A41, TCTN3, CTSL, MMRN1, CST1, ZIC1, AIRE, SLCO6A1, TBC1D22B, POC5, SF3A1, CCDC103, NONO, BPNT1, HSPD1RASGRF1MARK3, YWHAB, HRAS, PPP1R9B, MYC, EHD4, ADRBK1, CEBPA, SNRNP70, SRC, SRPK2


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 CTSH_RASGRF1


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 CTSH_RASGRF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCTSHC0011854Diabetes Mellitus, Insulin-Dependent1CTD_human
HgeneCTSHC0023467Leukemia, Myelocytic, Acute1CTD_human
TgeneRASGRF1C0005586Bipolar Disorder1PSYGENET
TgeneRASGRF1C0013386Dyskinesia, Drug-Induced1CTD_human
TgeneRASGRF1C0027092Myopia1CTD_human
TgeneRASGRF1C0034951Refractive Errors1CTD_human