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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: 38544

FusionGeneSummary for TMEM216_PGM3

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM216_PGM3
Fusion gene ID: 38544
HgeneTgene
Gene symbol

TMEM216

PGM3

Gene ID

51259

5238

Gene nametransmembrane protein 216phosphoglucomutase 3
SynonymsHSPC244AGM1|IMD23|PAGM|PGM 3
Cytomap

11q12.2

6q14.1

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 216phosphoacetylglucosamine mutaseN-acetylglucosamine-phosphate mutase 1acetylglucosamine phosphomutase
Modification date2018052320180523
UniProtAcc

Q9P0N5

O95394

Ensembl transtripts involved in fusion geneENST00000515837, ENST00000334888, 
ENST00000398979, 
ENST00000513973, 
ENST00000512866, ENST00000283977, 
ENST00000506587, 
Fusion gene scores* DoF score2 X 3 X 2=123 X 3 X 3=27
# samples 23
** MAII scorelog2(2/12*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TMEM216 [Title/Abstract] AND PGM3 [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
TCGALDPRADTCGA-HC-7233-01ATMEM216chr11

61161448

+PGM3chr6

83898517

-
* 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-shiftENST00000515837ENST00000513973TMEM216chr11

61161448

+PGM3chr6

83898517

-
Frame-shiftENST00000515837ENST00000512866TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000515837ENST00000283977TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000515837ENST00000506587TMEM216chr11

61161448

+PGM3chr6

83898517

-
Frame-shiftENST00000334888ENST00000513973TMEM216chr11

61161448

+PGM3chr6

83898517

-
Frame-shiftENST00000334888ENST00000512866TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000334888ENST00000283977TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000334888ENST00000506587TMEM216chr11

61161448

+PGM3chr6

83898517

-
Frame-shiftENST00000398979ENST00000513973TMEM216chr11

61161448

+PGM3chr6

83898517

-
Frame-shiftENST00000398979ENST00000512866TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000398979ENST00000283977TMEM216chr11

61161448

+PGM3chr6

83898517

-
5CDS-5UTRENST00000398979ENST00000506587TMEM216chr11

61161448

+PGM3chr6

83898517

-

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FusionProtFeatures for TMEM216_PGM3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TMEM216

Q9P0N5

PGM3

O95394

Part of the tectonic-like complex which is required fortissue-specific ciliogenesis and may regulate ciliary membranecomposition. {ECO:0000269|PubMed:22282472}.

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 TMEM216_PGM3


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 TMEM216_PGM3


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
TMEM216MCM3AP, ELAVL1, ACBD3, ACSL3, AGPAT1, AGPAT6, AGPAT9, ALG9, ANKLE2, ANO10, ANO6, ARFGAP3, ARHGAP1, ARL6IP5, ATP6AP1, ATP6AP2, AUP1, BCAP31, BET1, BET1L, CAMLG, CCDC47, CD99, CD99L2, CDCA3, CDKAL1, CERS2, CHP1, CISD2, CKAP4, CLCC1, CLCN7, EMC8, CPD, CTNND1, CXADR, CYB5B, DDRGK1, DHRS7, DNAJC1, EFNB1, EFNB2, EIF2AK3, EMD, ESYT1, FAM91A1, GBA2, GOLGA3, GOLGA5, GOLT1B, GOPC, GORASP2, GOSR1, GPR107, GPR89A, HMOX2, IGF2R, ITGB1, ITM2C, JAGN1, JPH1, EMC1, KIAA1715, KTN1, LBR, LEMD3, LMAN1, LOC100506055, LPCAT1, LRRC59, LSR, LYSMD3, MARCKSL1, MCAM, MMGT1, MTDH, NCOA2, NSDHL, NUP155, NUP35, OCLN, OSBP, OSBPL8, PDCL, PDXDC1, PDZD8, PGRMC2, POR, PREB, PTPN1, PVRL2, RAB7A, RABL3, RELL1, RER1, RHBDD2, ROR2, RTN4, SCAMP1, SCFD1, SCYL3, SEC11A, SEC22B, SEC24B, SEC63, SEMA6A, SFT2D3, SGPL1, SLC12A2, SLC12A4, SLC1A5, SLC20A2, SLC30A5, SLC30A6, SLC33A1, SLC38A1, SLC38A2, SLC39A10, SLC39A6, SLC39A7, SLC3A2, SLC4A7, SLC6A15, SLC6A8, SLC6A9, SLC7A5, SMPD4, SNAP23, SPCS2, SRPR, STAM, STEAP3, STIM1, STX10, STX12, STX5, STX6, STX7, STX8, TEX264, TFRC, EMC3, TMEM115, TMEM199, TMEM209, TMEM214, NDC1, TMEM51, TMEM87A, TMEM9, TMPO, TMX1, TMX4, TOR1AIP1, TRIM13, EMC2, UBE2J1, UBXN4, USE1, VAMP2, VAMP3, VANGL1, VAPA, VAPB, VEZT, VMA21, VMP1, VRK2, WDR11, WDR41, YKT6, ABCE1, ALDH3A2, APBB1, APP, ARCN1, ARFGAP2, ARFIP1, ATP6V0A1, ATP6V1F, BSDC1, EMC7, THEM6, CAV1, CCDC115, CLINT1, COPB1, COPG1, DSC2, DSG2, EBAG9, EPHA2, EPHA7, F11R, FAM134B, FKBP8, FZD6, GORAB, GPR108, IRS4, JAG2, KIAA0319L, PALD1, LNPEP, LRBA, LSG1, MARVELD2, MB21D2, MOSPD2, OSBPL11, PKMYT1, PLD3, PTPN2, SCARB1, SEC23B, SEC23IP, SENP2, SLC19A1, SLC39A14, SLC6A6, SOAT1, SPCS3, SRPRB, SSR1, STAM2, STT3B, STX18, SUN1, SYAP1, TBC1D22B, TEX2, TMEM109, TMEM57, TMF1, TOR1AIP2, UBE2G2, UBIAD1, UGT8, UNC5B, VANGL2, VAT1, VKORC1L1, WDR6, LPHN2PGM3CUL3, SPRTN, APP, BAG3, DCP2, ENOPH1, HDHD1, LACTB2, GLO1, PGM1, PGM5, UAP1, NTRK1, GAN, ZNF746, BDH1, QTRTD1, MARC1


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 TMEM216_PGM3


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 TMEM216_PGM3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTMEM216C1842577JOUBERT SYNDROME 24CTD_human;UNIPROT
HgeneTMEM216C1864148MECKEL SYNDROME, TYPE 21CTD_human;UNIPROT
TgenePGM3C4014371IMMUNODEFICIENCY 233ORPHANET;UNIPROT