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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: 26375

FusionGeneSummary for PDE1C_LAT2

check button Fusion gene summary
Fusion gene informationFusion gene name: PDE1C_LAT2
Fusion gene ID: 26375
HgeneTgene
Gene symbol

PDE1C

LAT2

Gene ID

5137

23428

Gene namephosphodiesterase 1Csolute carrier family 7 member 8
SynonymsHcam3|cam-PDE 1C|hCam-3LAT2|LPI-PC1
Cytomap

7p14.3

14q11.2

Type of geneprotein-codingprotein-coding
Descriptioncalcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1CHuman 3',5' cyclic nucleotide phosphodiesterase (HSPDE1C1A)phosphodiesterase 1C, calmodulin-dependent 70kDalarge neutral amino acids transporter small subunit 2L-type amino acid transporter 2integral membrane protein E16Hsolute carrier family 7 (amino acid transporter light chain, L system), member 8solute carrier family 7 (amino acid transporter, L-type),
Modification date2018051920180523
UniProtAcc

Q14123

Q9GZY6

Ensembl transtripts involved in fusion geneENST00000396193, ENST00000396191, 
ENST00000321453, ENST00000396184, 
ENST00000479980, ENST00000396182, 
ENST00000344995, ENST00000460943, 
ENST00000398475, ENST00000275635, 
Fusion gene scores* DoF score3 X 3 X 2=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: PDE1C [Title/Abstract] AND LAT2 [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
TgeneLAT2

GO:0006865

amino acid transport

10391915|10574970|15918515


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
ChiTaRS3.1AV724221PDE1Cchr7

32088724

-LAT2chr7

73643778

+
* 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-3UTRENST00000396193ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396193ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000396193ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396193ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396191ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396191ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000396191ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396191ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000321453ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000321453ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000321453ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000321453ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396184ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396184ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000396184ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396184ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000479980ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000479980ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000479980ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000479980ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396182ENST00000344995PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396182ENST00000460943PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-intronENST00000396182ENST00000398475PDE1Cchr7

32088724

-LAT2chr7

73643778

+
intron-3UTRENST00000396182ENST00000275635PDE1Cchr7

32088724

-LAT2chr7

73643778

+

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FusionProtFeatures for PDE1C_LAT2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PDE1C

Q14123

LAT2

Q9GZY6

Cyclic nucleotide phosphodiesterase with a dual-specificity for the second messengers cAMP and cGMP, which are keyregulators of many important physiological processes. Has a highaffinity for both cAMP and cGMP. Involved in FCER1 (high affinity immunoglobulin epsilonreceptor)-mediated signaling in mast cells. May also be involvedin BCR (B-cell antigen receptor)-mediated signaling in B-cells andFCGR1 (high affinity immunoglobulin gamma Fc receptor I)-mediatedsignaling in myeloid cells. Couples activation of these receptorsand their associated kinases with distal intracellular eventsthrough the recruitment of GRB2. {ECO:0000269|PubMed:12486104,ECO:0000269|PubMed:12514734, ECO:0000269|PubMed:15010370}.

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 PDE1C_LAT2


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 PDE1C_LAT2


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


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RelatedDrugs for PDE1C_LAT2


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 PDE1C_LAT2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePDE1CC0236969Substance-Related Disorders1CTD_human