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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: 15485

FusionGeneSummary for GRN_NCALD

check button Fusion gene summary
Fusion gene informationFusion gene name: GRN_NCALD
Fusion gene ID: 15485
HgeneTgene
Gene symbol

GRN

NCALD

Gene ID

2896

83988

Gene namegranulin precursorneurocalcin delta
SynonymsCLN11|GEP|GP88|PCDGF|PEPI|PGRN-
Cytomap

17q21.31

8q22.3

Type of geneprotein-codingprotein-coding
DescriptiongranulinsPC cell-derived growth factoracrograningranulin-epithelinproepithelinprogranulinneurocalcin-delta
Modification date2018052220180519
UniProtAcc

P28799

P61601

Ensembl transtripts involved in fusion geneENST00000053867, ENST00000589265, 
ENST00000589923, 
ENST00000311028, 
ENST00000395923, ENST00000220931, 
ENST00000521599, ENST00000522951, 
ENST00000519508, ENST00000521371, 
Fusion gene scores* DoF score13 X 10 X 6=78015 X 8 X 9=1080
# samples 1919
** MAII scorelog2(19/780*10)=-2.03747470541866
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1080*10)=-2.50695998871988
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GRN [Title/Abstract] AND NCALD [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
TCGARVBRCATCGA-D8-A1X6-01AGRNchr17

42430470

+NCALDchr8

102813898

-
* 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-intronENST00000053867ENST00000311028GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000395923GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000220931GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000521599GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000522951GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000519508GRNchr17

42430470

+NCALDchr8

102813898

-
5CDS-intronENST00000053867ENST00000521371GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000311028GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000395923GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000220931GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000521599GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000522951GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000519508GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589265ENST00000521371GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000311028GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000395923GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000220931GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000521599GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000522951GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000519508GRNchr17

42430470

+NCALDchr8

102813898

-
intron-intronENST00000589923ENST00000521371GRNchr17

42430470

+NCALDchr8

102813898

-

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FusionProtFeatures for GRN_NCALD


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

P28799

NCALD

P61601

May be involved in the calcium-dependent regulation ofrhodopsin phosphorylation. Binds three calcium ions.

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 GRN_NCALD


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 GRN_NCALD


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
GRNCCNT1, FAM131C, HOXA1, CDK9, TAT, SLPI, DLK1, TOP3B, TRIB3, ATXN7, CACNA1A, SIRT3, VHL, CRKL, CDK2, ATN1, GFI1B, FBXO6, SMAD9, CFTR, NPM1, FRAT1, TGM2, KRT18, RAC1, CCNG1, CRY1, PIK3R2, PRKAB2, YY1, POT1, HECW2, RPS6KA1, DLX2, OTX1, SGTA, GLRX3, NLK, FANCL, ARFGAP1, CCDC33, KRTAP10-7, KRTAP26-1, NXF1, CUL7, CCDC8, EED, EGFR, CELA2B, CD68, OBFC1, CTSO, SAV1, CLEC4M, PKP2, GNB2, FLYWCH2, FAM207A, AHCYL2, PPP2CA, ZC3HC1, DCP1B, COX6B1, TLE3, EGFL7, OTUD5, NAPSA, SPACA4, ZFP41, NTRK1, NF2, DNAJC10, NAB2, C7orf60, DEFA1, CACNG5, PLA2G10, FAM19A3, ZNF408, AGRP, RAPGEF6, CCDC69, ZNF517, ATP1B3, ABI2, ADAMTSL1, C1orf106, WFDC2, EDC3, SERPING1, BRCA1NCALDDTX2, ACTB, METTL21A, MEOX2, C1QTNF2, ARMC1, HAX1, NUFIP1, DGUOK, DNAAF2, TMEM14B, NDUFB5, VTCN1, HSPBAP1


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 GRN_NCALD


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 GRN_NCALD


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGRNC0011570Mental Depression3PSYGENET
HgeneGRNC0011581Depressive disorder3HPO;PSYGENET
HgeneGRNC0005586Bipolar Disorder2PSYGENET
HgeneGRNC0036341Schizophrenia2PSYGENET
HgeneGRNC0338451Frontotemporal dementia2CTD_human;HPO
HgeneGRNC0497327Dementia2CTD_human
HgeneGRNC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneGRNC0027746Nerve Degeneration1CTD_human
HgeneGRNC0751072Frontotemporal Lobar Degeneration1CTD_human
HgeneGRNC1843792FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED1CTD_human;UNIPROT