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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: 17523

FusionGeneSummary for INPP5E_SEC16A

check button Fusion gene summary
Fusion gene informationFusion gene name: INPP5E_SEC16A
Fusion gene ID: 17523
HgeneTgene
Gene symbol

INPP5E

SEC16A

Gene ID

56623

9919

Gene nameinositol polyphosphate-5-phosphatase ESEC16 homolog A, endoplasmic reticulum export factor
SynonymsCORS1|CPD4|JBTS1|MORMS|PPI5PIV|pharbinKIAA0310|SEC16L|p250
Cytomap

9q34.3

9q34.3

Type of geneprotein-codingprotein-coding
Description72 kDa inositol polyphosphate 5-phosphatasephosphatidylinositol polyphosphate 5-phosphatase type IVphosphatidylinositol-4,5-bisphosphate 5-phosphataseprotein transport protein Sec16Aprotein SEC16 homolog A
Modification date2018052220180523
UniProtAcc

Q9NRR6

O15027

Ensembl transtripts involved in fusion geneENST00000371712, ENST00000313050, 
ENST00000467838, ENST00000371706, 
ENST00000313084, ENST00000290037, 
ENST00000431893, ENST00000398335, 
Fusion gene scores* DoF score4 X 4 X 4=644 X 4 X 4=64
# samples 44
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: INPP5E [Title/Abstract] AND SEC16A [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
TgeneSEC16A

GO:0007029

endoplasmic reticulum organization

21768384


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
TCGARVLUSCTCGA-56-6546-01AINPP5Echr9

139328489

-SEC16Achr9

139352036

-
* 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-shiftENST00000371712ENST00000313050INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000467838INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000371706INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000313084INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000290037INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000431893INPP5Echr9

139328489

-SEC16Achr9

139352036

-
5CDS-intronENST00000371712ENST00000398335INPP5Echr9

139328489

-SEC16Achr9

139352036

-

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FusionProtFeatures for INPP5E_SEC16A


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
INPP5E

Q9NRR6

SEC16A

O15027

Converts phosphatidylinositol 3,4,5-trisphosphate(PtdIns 3,4,5-P3) to PtdIns-P2, and phosphatidylinositol 4,5-bisphosphate to phosphatidylinositol 4-phosphate. Specific forlipid substrates, inactive towards water soluble inositolphosphates. {ECO:0000269|PubMed:10764818}. Defines endoplasmic reticulum exit sites (ERES) and isrequired for secretory cargo traffic from the endoplasmicreticulum to the Golgi apparatus. SAR1A-GTP-dependent assembly ofSEC16A on the ER membrane forms an organized scaffold defining anERES. Required for normal transitional endoplasmic reticulum (tER)organization. {ECO:0000269|PubMed:17005010,ECO:0000269|PubMed:17192411}.

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 INPP5E_SEC16A


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 INPP5E_SEC16A


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
INPP5EPDE6D, KCTD3, CGN, KIF13B, ZBTB21, KSR1, RALGPS2, GIGYF1, RTKN, MAST3, LPIN3, LRFN1, GIGYF2, CDC25C, DENND4C, NF1, PPM1H, CBY1, SH3RF3, DENND1A, SH3PXD2A, SRGAP2, CAMSAP2, TANC2, PTPN13, EIF4E2, OSBPL6, SIPA1L1, HDAC4, NADK, RASAL2, LIMA1, MAGI1, KIAA1804, TESK2, DCLK1, MAPKAP1, TIAM1, KIF1C, ZNF638, NAV1, PLEKHA7, PHLDB2, STARD13, PTPN14, DENND4A, CWC25, RAB11FIP2, RPTOR, HDAC7, MTFR1L, RPGR, CEP170, DCAF7, YWHAESEC16ANFKB2, TERF1, TERF2, SIRT7, TSG101, CUL3, CAND1, SHC1, VCP, IQCB1, TRAF3, USO1, TRAF2, PAN2, SOX2, HDAC6, HDAC8, HDAC11, ANKRD28, LATS1, LATS2, SAV1, FKBP3, KRT18, CSNK1A1, CSNK1E, CEP250, EMD, CCDC8, RNF2, IRAK1, KLK15, AHNAK, HNRNPH3, NTRK1, MED23, CENPJ, XPO1, AP2A1, C4BPA, CAD, CLTA, CLTB, CLTC, DCTN1, DSP, ERF, GAK, GOLGA2, HNRNPA1, HNRNPK, IMPDH1, IMPDH2, HNRNPM, PFDN2, PIK3C2A, PKP2, PRKAR2A, RBM4, ATXN2, SEC13, TRPS1, VCL, ZKSCAN1, CLTCL1, TNK1, HDAC3, FUBP3, P4HA2, MAP7, BAG3, RBM39, NCOR2, SEC24C, CLINT1, PUM1, SMG7, CAPZA2, CDK2, DBN1, MYH9, PPP1CB, PRKAR2B, PICALM, IQGAP1, SYNPO, MAPRE1, TRIM29, LIMA1, GTSE1, MYO19, CDKN2AIPNL, ELMSAN1, ARX, FAM83H, MYO18A, HELZ, SEC24B, RBM14, SEC23B, SEC23A, SEC24A, PPP1R13L, PKP3, BTBD3, SPG20, FAM120A, KANK2, AKAP8L, PLEKHA5, ANKHD1, FAM120C, PIH1D1, WDR33, BMP2K, KIAA1217, EIF4ENIF1, CCAR2, P3H1, CPSF7, FIP1L1, FAM83D, CHD6, PRRC2B, FAM83A, WDR92, HNRNPUL2, FAM83B, CRY2, MCM2, RC3H1, MYO6, EGFR, EYA2, NEFL, XPNPEP3, AIPL1, PDHA1, BRCA1, YAP1, TES


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 INPP5E_SEC16A


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 INPP5E_SEC16A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneINPP5EC0431399Familial aplasia of the vermis3CTD_human;ORPHANET;UNIPROT
HgeneINPP5EC0008780Ciliary Motility Disorders2CTD_human
HgeneINPP5EC0015398Eye Diseases, Hereditary1CTD_human
HgeneINPP5EC0028754Obesity1CTD_human
HgeneINPP5EC0030846Penile Diseases1CTD_human
HgeneINPP5EC3714756Intellectual Disability1CTD_human