FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 35558

FusionGeneSummary for SPARC_NPLOC4

check button Fusion gene summary
Fusion gene informationFusion gene name: SPARC_NPLOC4
Fusion gene ID: 35558
HgeneTgene
Gene symbol

SPARC

NPLOC4

Gene ID

6678

55666

Gene namesecreted protein acidic and cysteine richNPL4 homolog, ubiquitin recognition factor
SynonymsBM-40|OI17|ONNPL4
Cytomap

5q33.1

17q25.3

Type of geneprotein-codingprotein-coding
DescriptionSPARCbasement-membrane protein 40secreted protein, acidic, cysteine-rich (osteonectin)nuclear protein localization protein 4 homologNPLOC4 ubiquitin recognition factornuclear protein localization 4 homolog
Modification date2018052320180523
UniProtAcc

P09486

Q8TAT6

Ensembl transtripts involved in fusion geneENST00000231061, ENST00000537849, 
ENST00000331134, ENST00000374747, 
ENST00000539314, ENST00000572760, 
ENST00000573876, ENST00000574344, 
Fusion gene scores* DoF score12 X 16 X 5=9609 X 7 X 8=504
# samples 1811
** MAII scorelog2(18/960*10)=-2.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/504*10)=-2.19592020997526
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SPARC [Title/Abstract] AND NPLOC4 [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
HgeneSPARC

GO:0001937

negative regulation of endothelial cell proliferation

12867428

HgeneSPARC

GO:0010595

positive regulation of endothelial cell migration

12867428

HgeneSPARC

GO:0016525

negative regulation of angiogenesis

12867428

HgeneSPARC

GO:0022604

regulation of cell morphogenesis

15389586


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
ChiTaRS3.1AA426012SPARCchr5

151042127

+NPLOC4chr17

79524285

+
* 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
intron-3UTRENST00000231061ENST00000331134SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000231061ENST00000374747SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000231061ENST00000539314SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000231061ENST00000572760SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000231061ENST00000573876SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000231061ENST00000574344SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-3UTRENST00000537849ENST00000331134SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000537849ENST00000374747SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000537849ENST00000539314SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000537849ENST00000572760SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000537849ENST00000573876SPARCchr5

151042127

+NPLOC4chr17

79524285

+
intron-intronENST00000537849ENST00000574344SPARCchr5

151042127

+NPLOC4chr17

79524285

+

Top

FusionProtFeatures for SPARC_NPLOC4


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

P09486

NPLOC4

Q8TAT6

Appears to regulate cell growth through interactionswith the extracellular matrix and cytokines. Binds calcium andcopper, several types of collagen, albumin, thrombospondin, PDGFand cell membranes. There are two calcium binding sites; an acidicdomain that binds 5 to 8 Ca(2+) with a low affinity and an EF-handloop that binds a Ca(2+) ion with a high affinity. The ternary complex containing UFD1, VCP and NPLOC4binds ubiquitinated proteins and is necessary for the export ofmisfolded proteins from the ER to the cytoplasm, where they aredegraded by the proteasome. The NPLOC4-UFD1-VCP complex regulatesspindle disassembly at the end of mitosis and is necessary for theformation of a closed nuclear envelope (By similarity). Acts as anegative regulator of type I interferon production via the complexformed with VCP and UFD1, which binds to DDX58/RIG-I and recruitsRNF125 to promote ubiquitination and degradation of DDX58/RIG-I(PubMed:26471729). {ECO:0000250|UniProtKB:Q9ES54,ECO:0000269|PubMed:26471729}.

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


Top

FusionGeneSequence for SPARC_NPLOC4


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).

Top

FusionGenePPI for SPARC_NPLOC4


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


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


Top

RelatedDrugs for SPARC_NPLOC4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneSPARCP09486DB11093Calcium CitrateSPARCsmall moleculeapproved
HgeneSPARCP09486DB11348Calcium PhosphateSPARCsmall moleculeapproved

Top

RelatedDiseases for SPARC_NPLOC4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSPARCC0023893Liver Cirrhosis, Experimental2CTD_human
HgeneSPARCC0009375Colonic Neoplasms1CTD_human
HgeneSPARCC0009404Colorectal Neoplasms1CTD_human
HgeneSPARCC0019158Hepatitis1CTD_human
HgeneSPARCC0020429Hyperalgesia1CTD_human
HgeneSPARCC0022658Kidney Diseases1CTD_human
HgeneSPARCC0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneSPARCC0023890Liver Cirrhosis1CTD_human
HgeneSPARCC0024031Low Back Pain1CTD_human
HgeneSPARCC0026764Multiple Myeloma1CTD_human
HgeneSPARCC0027540Necrosis1CTD_human
HgeneSPARCC0027659Neoplasms, Experimental1CTD_human
HgeneSPARCC0029434Osteogenesis Imperfecta1CTD_human
HgeneSPARCC0041948Uremia1CTD_human
HgeneSPARCC0043094Weight Gain1CTD_human
HgeneSPARCC0151744Myocardial Ischemia1CTD_human
HgeneSPARCC0158266Intervertebral Disc Degeneration1CTD_human
HgeneSPARCC0206686Adrenocortical carcinoma1CTD_human
HgeneSPARCC0919267ovarian neoplasm1CTD_human
HgeneSPARCC4225301OSTEOGENESIS IMPERFECTA, TYPE XVII1UNIPROT