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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: 2210

FusionGeneSummary for APOC1_SLC38A4

check button Fusion gene summary
Fusion gene informationFusion gene name: APOC1_SLC38A4
Fusion gene ID: 2210
HgeneTgene
Gene symbol

APOC1

SLC38A4

Gene ID

341

55089

Gene nameapolipoprotein C1solute carrier family 38 member 4
SynonymsApo-CI|ApoC-I|apo-CIB|apoC-IBATA3|NAT3|PAAT|SNAT4
Cytomap

19q13.32

12q13.11

Type of geneprotein-codingprotein-coding
Descriptionapolipoprotein C-Isodium-coupled neutral amino acid transporter 4N amino acid transporter 3Na(+)-coupled neutral amino acid transporter 4amino acid transporter A3amino acid transporter system A3system A amino acid transporter 3system N amino acid transporter 3
Modification date2018051920180527
UniProtAcc

P02654

Q969I6

Ensembl transtripts involved in fusion geneENST00000588750, ENST00000588802, 
ENST00000252491, ENST00000592885, 
ENST00000589781, ENST00000586638, 
ENST00000447411, ENST00000266579, 
Fusion gene scores* DoF score4 X 2 X 4=321 X 1 X 1=1
# samples 41
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: APOC1 [Title/Abstract] AND SLC38A4 [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
HgeneAPOC1

GO:0010900

negative regulation of phosphatidylcholine catabolic process

2302419

HgeneAPOC1

GO:0010916

negative regulation of very-low-density lipoprotein particle clearance

1917954

HgeneAPOC1

GO:0032375

negative regulation of cholesterol transport

10978346

HgeneAPOC1

GO:0033344

cholesterol efflux

11162594

HgeneAPOC1

GO:0033700

phospholipid efflux

11162594

HgeneAPOC1

GO:0034369

plasma lipoprotein particle remodeling

10978346

HgeneAPOC1

GO:0034382

chylomicron remnant clearance

4020294

HgeneAPOC1

GO:0045717

negative regulation of fatty acid biosynthetic process

15576844

HgeneAPOC1

GO:0045833

negative regulation of lipid metabolic process

182536

HgeneAPOC1

GO:0048261

negative regulation of receptor-mediated endocytosis

1917954

HgeneAPOC1

GO:0050995

negative regulation of lipid catabolic process

15576844

HgeneAPOC1

GO:0051005

negative regulation of lipoprotein lipase activity

15576844


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
TCGARVLIHCTCGA-2Y-A9HB-01AAPOC1chr19

45422606

+SLC38A4chr12

47226191

-
* 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-intronENST00000588750ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
intron-intronENST00000588750ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000588802ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000588802ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000252491ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000252491ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000592885ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000592885ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000589781ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000589781ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000586638ENST00000447411APOC1chr19

45422606

+SLC38A4chr12

47226191

-
5CDS-intronENST00000586638ENST00000266579APOC1chr19

45422606

+SLC38A4chr12

47226191

-

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FusionProtFeatures for APOC1_SLC38A4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
APOC1

P02654

SLC38A4

Q969I6

Inhibitor of lipoprotein binding to the low densitylipoprotein (LDL) receptor, LDL receptor-related protein, and verylow density lipoprotein (VLDL) receptor. Associates with highdensity lipoproteins (HDL) and the triacylglycerol-richlipoproteins in the plasma and makes up about 10% of the proteinof the VLDL and 2% of that of HDL. Appears to interfere directlywith fatty acid uptake and is also the major plasma inhibitor ofcholesteryl ester transfer protein (CETP). Binds free fatty acidsand reduces their intracellular esterification. Modulates theinteraction of APOE with beta-migrating VLDL and inhibits bindingof beta-VLDL to the LDL receptor-related protein.{ECO:0000269|PubMed:17339654, ECO:0000303|PubMed:25160599}. Sodium-dependent amino acid transporter. Mediateselectrogenic symport of neutral amino acids and sodium ions. Has abroad specificity, with a preference for Ala, followed by His,Cys, Asn, Ser, Gly, Val, Thr, Gln and Met. May mediate sodium-independent transport of cationic amino acids, such as Arg andLys. Amino acid uptake is pH-dependent, with low transportactivities at pH 6.5, intermediate at pH 7.0 and highest betweenpH 7.5 and 8.5. {ECO:0000269|PubMed:11342143,ECO:0000269|PubMed:11414754}.

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 APOC1_SLC38A4


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 APOC1_SLC38A4


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
APOC1APOA1, HMP19, VKORC1, ALBSLC38A4


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 APOC1_SLC38A4


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 APOC1_SLC38A4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAPOC1C0018801Heart failure1CTD_human